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'''Marcus Theory''' is a theory originally developed by [[Rudolph A. Marcus]], starting in 1956, to explain the rates of [[electron transfer]] reactions &ndash; the rate at which an electron can move or jump from one chemical species (called the electron donor) to another (called the electron acceptor).<ref name="Nobel">{{internetquelle|werk=Nobelstiftung|url=http://nobelprize.org/nobel_prizes/chemistry/laureates/1992/marcus-lecture.pdf |titel=Electron Transfer Reactions in Chemistry: Theory and Experiment|zugriff=02.04.2007}}</ref> It was originally formulated to address [[outer sphere electron transfer]] reactions, in which the two chemical species only change in their charge with an electron jumping (e.g. the oxidation of an ion like Fe<sup>2+</sup>/Fe<sup>3+</sup>), but do not undergo large structural changes. It was extended to include [[inner sphere electron transfer]] contributions, in which a change of distances or geometry in the solvation or coordination shells of the two chemical species is taken into account (the Fe-O distances in Fe(H<sub>2</sub>O)<sup>2+</sup> and Fe(H<sub>2</sub>O)<sup>3+</sup> are different).<ref>Contrary to Marcus' approach the inner sphere electron transfer theory of [[Noel S. Hush]] refers to a ''continuous'' change of the electron density during transfer along a geometrical coordinate (adiabatic case), and takes also into account the solvent influence as did Marcus. Hush's formulation is known as Marcus-Hush theory.</ref><ref name="Hush">Hush, N.S. Trans. Faraday Soc. 1961, '''57''',557</ref>


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For redox reactions without making or breaking bonds '''Marcus theory''' takes the place of Eyring's [[transition state theory]] <ref name="TST1">P. W. Atkins: ''Physical Chemistry'', 6. Ed., Oxford University Press, Oxford 1998 p.830</ref><ref name="TST2">R.S. Berry, S. A. Rice, J. Ross: ''Physical Chemistry'', Wiley, New York 1980, S. 1147 ff,</ref> which has been derived for reactions with structural changes. Both theories lead to rate equations of the same exponential form. However, whereas in Eyring theory the reaction partners become strongly coupled in the course of the reaction to form a structurally defined activated complex, in Marcus theory they are weakly coupled and retain their individuality. It is the thermally induced reorganization of the surroundings, the solvent (outer sphere) and the solvent sheath or the ligands (inner sphere) which create the geometrically favourable situation ''prior'' to and independent of the electron jump.  
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The original classical Marcus theory for outer sphere electron transfer reactions demonstrates the importance of the solvent and leads the way to the calculation of the [[Gibbs free energy]] of activation, using the [[Polarization (electrochemistry)|polarization]] properties of the solvent, the size of the reactants, the transfer distance and the Gibbs free energy <math>\Delta</math>G<sup>0</sup> of the redox reaction. The most startling result of Marcus' theory was the "inverted region": whereas the reaction rates usually become higher with increasing [[Exergonic reaction|exergonicity]] of the reaction, electron transfer should, according to Marcus theory, become slower in the  very negative <math>\Delta</math>G<sup>0</sup> domain. The inverted region was searched for 30 years until it was unequivocally verified experimentally in 1984. 


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R.A. Marcus received the [[Nobel Prize in Chemistry]] in 1992 for this theory. Marcus theory is used to describe a number of important processes in chemistry and biology, including [[photosynthesis]], [[corrosion]], certain types of [[chemiluminescence]], charge separation in some types of [[solar cells|solar cell]] and more. Besides the inner and outer sphere applications, Marcus theory has been extended to address [[heterogeneous electron transfer]].
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== The One-Electron Redox Reaction ==


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Chemical reactions may lead to a substitution of a group in a molecule or a ligand in a complex, to the elimination of a group of the molecule or a ligand, or to a rearrangement of a molecule or complex. A chemical reaction may, however, also cause simply an exchange of charges between the reactants, and these redox reactions without making or breaking a bond seem to be quite  simple in Inorganic Chemistry for ions and complexes. These reactions often become manifest by a change of colour, e.g. for ions or complexes of transition metal ions, but organic molecules, too, may change their colour by accepting or giving away an electron (like the herbicide [[Paraquat]] (4,4'-bipyridyl) which becomes blue when accepting an electron, thence the alternative name of methyl viologen). For this type of redox reactions R.A. Marcus has developed his theory. Here the trace of argument and the results are presented. For the mathematical development and details the original papers<ref name="Marcus 1">Marcus, R.A. "On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer I" ''J.Chem.Phys.''1956, '''24''', 966. {{DOI|10.1063/1.1742723}} or [http://www.cce.caltech.edu/faculty/marcus/publications/16.pdf Free Text]</ref><ref name="Marcus 2">Marcus.R.A. "Electrostatic Free Energy and Other Properties of States Having Nonequilibrium Polarization I. ''J.Chem.Phys.''1956, '''24''', 979. {{DOI|10.1063/1.1742724}} or [http://www.cce.caltech.edu/faculty/marcus/publications/17.pdf Free Text]</ref> should be consulted.  
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In a redox reaction one partner acts as an electron donor D the other as an acceptor A. For a reaction to take place D and A must diffuse together. They form the precursor complex, usually a kinetic, unstable, solvated encounter complex, which by electron transfer is transformed to the successor complex, and finally this separates by diffusion. For a one electron transfer the reaction is


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(D and A may already carry charges). Here k<sub>12</sub>, k<sub>21</sub> and k<sub>30</sub> are diffusion constants, k<sub>23</sub> and k<sub>32</sub> rate constants of activated reactions. The total reaction may be diffusion controlled (the electron transfer step is faster than diffusion, every encounter leads to reaction) or activation controlled (the "equilibrium of association" is reached, the electron transfer step is slow, the separation of the successor complex is fast).


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==Outer Sphere Electron Transfer==
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Redox reactions are preferably run in polar solvents. Donor and acceptor then have a solvent shell and the precursor and successor complexes are solvated also. The closest molecules of the solvent shell, or the ligands in complexes, are tightly bound and constitute the "inner sphere". Reactions in which these participate are called inner sphere redox reactions. The free solvent molecules constitute the "outer sphere". Outer sphere redox reactions do not change the inner sphere, no bonds are made nor broken.
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It was R.A. Marcus who realized the role of the solvent when he worked on the nature and magnitude of the Gibbs free energy of activation for redox reactions, more precisely: one-electron transfer reactions of the outer sphere type. He published two fundamental papers.<ref name="Marcus 1" /><ref name="Marcus 2" /> The ideas of these two papers are often referred to Marcus Theory although Marcus’ later work goes much beyond them.<ref name="Nobel"/> In the following the development and results of the ideas of these two papers are outlined. For the mathematics and more details the original papers should be consulted.


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In outer sphere redox reactions no bonds are formed or broken; only an electron transfer (ET) takes place. A quite simple example is the Fe<sup>2+</sup>/Fe<sup>3+</sup> redox reaction, the self exchange reaction which is known to be always occurring in an aqueous solution containing both FeSO<sub>4</sub> and Fe<sub>2</sub>(SO<sub>4</sub>)<sub>3</sub> (of course, with equal and measurable rates in both directions and with Gibbs free reaction energy <math>\Delta</math>G<sup>0</sup> = 0).


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From the reaction rate's temperature dependence (e.g. the S<sub>N2</sub>-substitution reaction of the saponification of an alkyl halide) an [[activation energy]] is determined, and this activation energy is interpreted as the energy of the [[transition state]] in a reaction diagram. The latter is drawn, according to Arrhenius and Eyring, as an energy diagram with the reaction coordinate as the abscissa. The reaction coordinate describes the minimum energy path from the reactants to the products, and the points of this coordinate are combinations of distances and angles between and in the reactants in the course of the formation and/or cleavage of bonds. The maximum of the energy diagram, the [[transition state]], is characterized by a specific configuration of the atoms. Moreover, in Eyring’s TST <ref name="TST1" /><ref name="TST2" /> a quite specific change of the [[nuclear coordinates]] is responsible for crossing the maximum point, a vibration in this direction is consequently treated as a translation.
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For outer sphere redox reactions there cannot be such a reaction path, but nevertheless one does observe an activation energy. The rate equation for activation-controlled reactions has the same exponential form as the Eyring equation,


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<math> \Delta G^{\ddagger}</math>is the Gibbs free energy of the formation of the transition state, the exponential term represents the probability of its formation, A contains the probability of crossing from precursor to successor complex.


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The consequence of an electron transfer is the rearrangement of charges, and this gravely influences the solvent environment. For the dipolar solvent molecules rearrange in the direction of the field of the charges (this is called orientation polarisation), and also the atoms and electrons in the solvent molecules are slightly displaced (atomic and electron polarization, respectively). It is this [[solvent polarization]] which determines the free energy of activation and thus the reaction rate.  


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Substitution, elimination and isomerization reactions differ from the outer sphere redox reaction not only in the structural changes outlined above, but also in the fact that the movements of the nuclei and the shift of charges ([[Intervalence charge transfer|charge transfer]], CT) on the reactions path take place in a continuous and concerted way: nuclear configurations and charge distribution are always “in equilibrium”. This is illustrated by the S<sub>N</sub>2 substitution of the saponification of an alkyl halide where the rear side attack of the OH<sup>-</sup> ion pushes out a halide ion and where a transition state with a five-coordinated carbon atom must be visualized. The system of the reactants becomes coupled so tightly during the reaction that they form the [[activated complex]] as an integral entity. The solvent here has a minor effect.
 
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By contrast, in outer sphere redox reactions the displacement of nuclei in the reactants are small, here the solvent has the dominant role. Donor-acceptor coupling is weak, both keep their identity during the reaction. Therefore the electron, being an elementary particle, can only “jump” as a whole ([[electron transfer]], ET). If the electron jumps, the transfer is much faster than the movement of the large solvent molecules, with the consequence that the nuclear positions of the reaction partners and the solvent molecules are the same before and after the electron jump ([[Franck-Condon principle]]).<ref>W.F. Libby, "Theory of Electron Exchange Reactions in Aquous Solution" ''J.Phys.Chem.'' 1952, '''56''', 863</ref> The jump of the electron is governed by quantum mechanical rules, it is only possible if  also the energy of the ET system does not change “during” the jump.


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The arrangement of solvent molecules depends on the charge distribution on the reactants. If the solvent configuration must be the same before and after the jump ''and'' the energy may not change, then the solvent cannot be in the solvation state of the precursor nor in that of the successor complex as they are different, it has to be somewhere in between. For the self-exchange reaction for symmetry reasons an arrangement of the solvent molecules exactly in the middle of those of precursor and successor complex would meet the conditions. This means that the solvent arrangement with half of the electron on both donor and acceptor would be the correct environment for jumping. Also, in this state the energy of precursor and successor in their solvent environment would be the same.  
 
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However, the electron as an elementary particle cannot be divided, it resides either on the donor or the acceptor and arranges the solvent molecules accordingly in an equilibrium. The “transition state”, on the other hand, requires a solvent configuration which would result from the transfer of half an electron, which is impossible. This means that real charge distribution and required solvent polarization are not in an “equilibrium”. Yet it is possible that the solvent takes a configuration corresponding to the “transition state”, even if the electron sits on the donor or acceptor. This, however, requires energy. This energy may be provided by the thermal energy of the solvent and [[thermal fluctuations]] can produce the correct polarization state. Once this has been reached the electron can jump. The ''creation'' of the correct solvent arrangement and the electron jump are decoupled and do not happen in a synchronous process. Thus the energy of the transition state is mostly polarization energy of the solvent.


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=== The Macroscopic System: Two Conducting Spheres ===


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On the basis of his reasoning R.A. Marcus developed a ''classical'' theory with the aim of calculating the polarization energy of the said non-equilibrium state. From thermodynamics it is well known that the energy of such a state can be determined if a reversible path to that state is found. Marcus was successful finding such a path via two reversible charging steps for the preparation of the “transition state” from the precursor complex.
 
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Four elements are essential for the model on which the theory is based: (1) Marcus employs a classical, purely electrostatic model. The charge (many elementary charges) may be transferred in any portion from one body to another. (2) Marcus separates the fast electron polarisation P<sub>e</sub> and the slow atom and orientation polarisation P<sub>u</sub> of the solvent on grounds of their time constants differing several orders of magnitude. (3) Marcus separates the inner sphere (reactant + tightly bound solvent molecules, in complexes + ligands) and the outer sphere (free solvent ) (4) In this model Marcus confines himself to calculating the outer sphere energy of the non-equilibrium polarization of the “transition state”. The outer sphere energy is often much larger than the inner sphere contribution because of the far reaching electrostatic forces (compare the [[Debye-Hückel theory]] of electrochemistry).


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Marcus’ tool is the theory of dielectric polarization in solvents. He solved the problem in a general way for a transfer of charge between two bodies of arbitrary shape with arbitrary surface and volume charge. For the self-exchange reaction, the redox pair (e.g. Fe(H<sub>2</sub>O)<sub>6</sub><sup>3+</sup> / Fe(H<sub>2</sub>O)<sub>6</sub><sup>2+</sup>) is substituted by two macroscopic conducting spheres at a defined distance carrying specified charges. Between these spheres a certain amount of charge is reversibly exchanged.
 
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In the first step the energy W<sub>I</sub> of the transfer of a specific amount of charge is calculated, e.g. for the system in a state when both spheres carry half of the amount of charge which is to be transferred. This state of the system can be reached by transferring the respective charge from the donor sphere to the vacuum and then back to the acceptor sphere.<ref>Marcus takes the vacuum state of the reactants as the zero energy point. Therefore many of his equations contain also the solvation energy of the isolated species W<sub>iso</sub> and the electrostatic energy of formation of the precursor and successor complexes.</ref>  Then the spheres in this state of charge give rise to a defined electric field in the solvent which creates the total solvent polarization P<sub>u</sub> + P<sub>e</sub>.  By the same token this polarization of the solvent interacts with the charges.


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In a second step the energy W<sub>II</sub> of the reversible (back) transfer of the charge to the first sphere, again via the vacuum, is calculated. However, ''the atom and orientation polarization P<sub>u</sub> is kept fixed'', only the electron polarization P<sub>e</sub> may adjust to the field of the new charge distribution ''and'' the fixed P<sub>u</sub>. After this second step the system is in the desired state with an electron polarization corresponding to the starting point of the redox reaction and an atom and orientation polarization corresponding to the “transition state”. The energy W<sub>I</sub> + W<sub>II</sub> of this state is, thermodynamically speaking, a Gibbs free energy G.  
 
  <li>[http://livinginplaya.net/read.php?1,299400 http://livinginplaya.net/read.php?1,299400]</li>
 
  <li>[http://www.nnzqm.com/forum.php?mod=viewthread&tid=1628297 http://www.nnzqm.com/forum.php?mod=viewthread&tid=1628297]</li>
 
  <li>[http://www.05931.cn/viewthread.php?tid=3449031&extra= http://www.05931.cn/viewthread.php?tid=3449031&extra=]</li>
 
  <li>[http://1.ts.cn/home.php?mod=space&uid=2660&do=blog&quickforward=1&id=5339098 http://1.ts.cn/home.php?mod=space&uid=2660&do=blog&quickforward=1&id=5339098]</li>
 
</ul>


== interesses Longchamp Le Pliage Tweedehands ==
[[Image:Marcusparabel.jpg|thumb|300px|Fig. 1. The parabolas of outer-sphere reorganisation energy of the system two spheres in a solvent. Parabola i: the charge on the first, transfer to the second, parabola f: the charge on the second, transfer to the first. The abscissa is the transferred amount of charge <math>\Delta</math>e or the induced polarization P, the ordinate the Gibbs free energy. ΔG(0)<sup>‡</sup> = λ<sub>o</sub>/4 is the reorganization energy at Δe = 0.5, it corresponds to the activation energy of the self-exchange reaction.]]


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Of course, in this classical model the transfer any arbitrary amount of charge <math>\Delta</math>e is possible. So the energy of the non-equilibrium state, and consequently of the polarization energy of the solvent,  can be probed as a function of <math>\Delta</math>e.  Thus Marcus has lumped together, in a very elegant way, the coordinates of all solvent molecules into a single coordinate of solvent polarization <math>\Delta</math>p which is determined by the amount of transferred charge <math>\Delta</math>e. So he reached a simplification of the energy representation to only two dimensions: G = f(<math>\Delta</math>e). The result for two conducting spheres in a solvent is the formula of Marcus
 
 
  <li>[http://ciarcr.org/spip.php?article310/ http://ciarcr.org/spip.php?article310/]</li>
<math> G =\left(\frac{1}{2r_{1}}+\frac{1}{2r_2}-\frac{1}{R}\right)\cdot\left(\frac{1}{\epsilon_{op}}-\frac{1}{\epsilon_s}\right)\cdot(\Delta e)^2  </math>
 
 
  <li>[http://enseignement-lsf.com/spip.php?article64#forum24579342 http://enseignement-lsf.com/spip.php?article64#forum24579342]</li>
Where r<sub>1</sub> and r<sub>2</sub> are the radii of the spheres and R is their separation, <math>\epsilon</math><sub>s</sub> and <math>\epsilon</math><sub>op</sub> are the static and high frequency (optical) dielectric constants of the solvent, <math>\Delta</math>e the amount of charge transferred. The graph of G vs. <math>\Delta</math>e is a parabola (Fig. 1). In Marcus theory the energy belonging to the transfer of a unit charge (<math>\Delta</math>e = 1) is called the (outer sphere) reorganization energy <math>\lambda</math><sub>o</sub>, i.e. the energy of a state where the polarization would correspond to the transfer of a unit amount of charge, but the real charge distribution is that before the transfer.<ref name= "square">Note: The quadratic dependence of outer sphere reorganization energy is ''not'' a consequence of vibrations in reactants or solvent!</ref> In terms of exchange direction the system is symmetric.
 
 
  <li>[http://enseignement-lsf.com/spip.php?article65#forum24260757 http://enseignement-lsf.com/spip.php?article65#forum24260757]</li>
=== The Microscopic System: The Redox Pair ===
 
 
  <li>[http://bbs.yapaifs.cn/forum.php?mod=viewthread&tid=4781062&fromuid=15088 http://bbs.yapaifs.cn/forum.php?mod=viewthread&tid=4781062&fromuid=15088]</li>
Shrinking the two-sphere model to the molecular level creates the problem that in the self exchange reaction the charge can no longer be transferred in arbitrary amounts, but only as a single electron. However, the polarization still is determined by the total ensemble of the solvent molecules and therefore can still be treated classically, i.e. the polarization energy is not subject to quantum limitations. Therefore the energy of solvent reorganization can be calculated as being due to a ''hypothetical'' transfer and back transfer of a partial elementary charge according to the Marcus formula. Thus the reorganization energy for chemical redox reactions, which is a Gibbs free energy, is also a parabolic function of <math>\Delta</math>e of this hypothetical transfer, For the self exchange reaction, where for symmetry reasons <math>\Delta</math>e = 0.5, the Gibbs free energy of activation is <math>\Delta</math>G(0)<sup>‡</sup> = <math>\lambda</math><sub>o</sub>/4 (see Fig. 1 and Fig.2 intersection of the parabolas I and f, f(0), respectively).
 
 
</ul>
Up to now all was physics, now some chemistry enters. The self exchange reaction is a very specific redox reaction, most of the redox reactions are between different partners <ref>they are often called Marcus cross reactions.</ref> e.g.
 
:<math>\mathrm{[Fe^{II}(CN)_{6}]^{4-}}+\mathrm{[Ir^{IV}Cl_{6}]^{2-}}\rightleftharpoons\mathrm{[Fe^{III}(CN)_{6}]^{3-}}+\mathrm{[Ir^{III}Cl_{6}]^{3-}}</math>
 
and they have positive (endergonic) or negative (exergonic) Gibbs free energies of reaction <math>\Delta</math>G<sup>0</sup>.
 
As Marcus calculations refer exclusively to the electrostatic properties in the solvent (outer sphere) <math>\Delta</math>G<sup>0</sup> and <math>\lambda</math><sub>o</sub> are independent of one another and therefore can just be added up. This means that the Marcus parabolas in systems with different <math>\Delta</math>G<sup>0</sup> are shifted just up or down in the G vs. <math>\Delta</math>e diagram (Fig. 2). Variation of <math>\Delta</math>G<sup>0</sup> can be affected in experiments by offering different acceptors to the same donor.  
 
Simple calculations of the points of intersection of the parabolas i (y = x<sup>2</sup>), f(0) (y = (x-d)<sup>2</sup>) and f1 to f3 (y = (x-d)<sup>2</sup> +c) give the Gibbs free energy of activation
 
:<math>\Delta G^{\ddagger} = \frac{(\lambda_{o} + \Delta G^0)^2}{4 \lambda_{o}}</math>
 
It should be noted that the intersection of those parabolas represents an activation energy and not the energy of a transition state of fixed configuration of all nuclei in the system as is the case in the substitution and other reactions mentioned. The transition state of the latter reactions has to meet structural and energetic conditions, redox reactions have only to comply to the energy requirement.  Whereas the geometry of the transition state in the other reactions is the same for all pairs of reactants, for redox pairs many polarization environments may meet the energetic conditions.
 
[[Image:Marcusparabel 2.jpg|thumb|300 px|Fig. 2 Marcus-Parabolas for different redox reactions: f<sub>1</sub> such with positive ΔG<sup>0</sup>, f(0) for the self-exchange reaction with ΔG<sup>0</sup> = 0 (broken line), f<sub>2</sub> for moderately negative ΔG<sup>0</sup> (selected so, that ΔG<sup>‡</sup> = 0) and f<sub>3</sub> for strongly negative ΔG<sup>0</sup>. The free energy of activation ΔG<sup>‡</sup> decreases from f<sub>1</sub> (b<sub>1</sub>) via f(0) (a) to f<sub>2</sub> (zero) and increases again for f<sub>3</sub> („Marcus inverted region“).]] 
 
Marcus’ formula shows a quadratic dependence of the Gibbs free energy of activation on the Gibbs free energy of reaction. It is general knowledge from the host of chemical experience that reactions usually are the faster the more negative is <math>\Delta</math>G<sup>0</sup>. In many cases even a linear free energy relation is found. According to the Marcus formula the rates increase also when the reactions are more exergonic, however only as long as <math>\Delta</math>G<sup>0</sup> is positive or slightly negative. It is surprising that for redox reactions according to the Marcus formula the activation energy should increase for very exergonic reaction, i.e. in the cases when <math>\Delta</math>G<sup>0</sup>is negative and its absolute value is greater than that of <math>\lambda</math><sub>o</sub>. This realm of Gibbs free energy of reaction is called “Marcus inverted region”. In Fig. 2 it becomes obvious that the intersection of the parabolas i and f moves upwards in the left part of the graph when <math>\Delta</math>G<sup>0</sup> continues to become more negative, and this means increasing activation energy. Thus the total graph of ln k vs. <math>\Delta</math>G<sup>0</sup> should have a maximum.
 
The maximum of the ET rate is expected at <math>\Delta</math>G<sup>‡</sup> = 0. Here <math>\Delta</math>e = 0  and q = 0 (Abb.2) which means that the electron may jump in the precursor complex at its equilibrium polarization. No thermal activation is necessary: the reaction is barrierless. In the inverted region the polarization corresponds to the difficult to imagine notion of a charge distribution where the donor has received and the acceptor given off charge. Of course, in real world this does not happen, it is not a real charge distribution which creates this critical polarization, but the thermal fluctuation in the solvent. This polarization necessary for transfer in the inverted region can be created – with some probability – as well as any other one.<ref>The reverse reaction may support understanding: for this reaction the polarization due to the hypothetical transfer of a unit electron charge is not sufficient to reach a polarization where the polarization energies of A/D and A<sup>-</sup>/D<sup>+</sup> are equal. This can only happen on the hypothetical transfer of more that one electron charge.</ref> The electron is just waiting for it for jumping.
 
==Inner Sphere Electron Transfer==
 
In the outer sphere model the donor or acceptor and the tightly bound solvation shells or the complex’ ligands  were considered to form rigid structures which do not change in the course of electron transfer. However, the distances in the inner sphere are dependent on the charge of donor and acceptor, e.g. the central ion-ligand distances are different in complexes carrying different charges  And again the Franck-Condon principle must be obeyed: for the electron to jump to occur, the nuclei have to have a configuration which is an identical one of as well the precursor as the successor complexes, of course highly distorted. In this case the energy requirement is fulfilled automatically.
 
In this inner sphere case the Arrhenius  concept holds, the transition state of definite geometric structure is reached along a geometrical reaction coordinate determined by nuclear motions. No further nuclear motion is necessary to form the successor complex, just the electron jumps, which makes a difference to the TST theory. The reaction coordinate for inner sphere energy is governed by vibrations and they differ in the oxidized and reduces species.<ref name= "Sutin">N. Sutin, 'Theory of Electron Transfer Reactions: Insights and Hindsights', Progr. Inorg. Chem. 1083, '''30''', 441-448</ref>
 
For the self-exchange system Fe<sup>2+</sup>/Fe<sup>3+</sup> only  the symmetrical breathing vibration of the six water molecules around the iron ions is considered.<ref name = "Sutin" /> Assuming harmonic conditions this vibration has frequencies <math>\nu_D</math> and <math>\nu_A</math>, the force constants f<sub>D</sub> and f<sub>A</sub> are <math>f = 4 \pi^2 \nu^2 \mu</math> and the energies are
:<math>E_D = E_D(q_{0,D}) + 3 f_D(\Delta q_D)^2</math>
:<math>E_A = E_A(q_{0,A}) + 3 f_A(\Delta q_A)^2</math>
where q<sub>0</sub> is the equilibrium normal coordinate and <math>\Delta q = (q-q_0) </math> the displacement along the normal coordinate, the factor 3 stems from 6 (H<sub>2</sub>O)<math>\cdot</math> ½. Like for the outer-sphere reorganization energy potential energy curve is quadratic, here, however, as a consequence of vibrations.  
 
The equilibrium normal coordinates differ in Fe(H<sub>2</sub>O)<sub>6</sub><sup>2+</sup> and Fe(H<sub>2</sub>O)<sub>6</sub><sup>3+</sup>. By thermal excitation of the breathing vibration a geometry can be reached which is common to both donor and acceptor, i.e. the potential energy curves of the breathing vibrations of D and A intersect here. This is the situation where the electron may jump. The energy of this transition state is the inner sphere reorganization energy <math>\lambda</math><sub>in</sub>.
For the self-exchange reaction the metal-water distance in the transition state can be calculated <ref name="Sutin"/>
 
:<math> q^*=\frac{f_D q_{0,D} + f_A q_{0,A}}{f_D + f_A} </math>
 
This gives the inner sphere reorganisation energy
:<math> \lambda_{in} = \Delta E^* = \frac{3 f_D f_A}{f_D + f_A}(q_{0,D} - q_{0,A})^2 </math>
 
It is fortunate that the expressions for the  energies for outer and inner reorganization have the same quadratic form. Inner sphere and outer sphere reorganization energies are independent, so they can be added to give <math>\lambda = \lambda_{in} + \lambda_o</math>  and inserted in the Arrhenius equation
 
<math> k_{act} = A \cdot e^{- \frac{ \Delta {G_{in}^{\ddagger}}+ \Delta {G_{o}}^{\ddagger}}{kT}}</math>
 
Here, A can be seen to represent the probability of electron jump, exp[-<math>\Delta</math>G<sub>in</sub><sup><math>^\ddagger</math></sup>/kT] that of reaching the transition state of the inner sphere and exp[-<math>\Delta</math>G<sub>o</sub><sup><math>^\ddagger</math></sup>/kT]  that of outer sphere adjustment .
For unsymmetrical (cross) reactions like
 
:<math>\mathrm{[Fe(H_2O)_6]^{2+}} +\mathrm{[[Co(H_2O)_6]]^{3+}} \rightleftharpoons \mathrm{[Fe(H_2O)_6]^{3+}} + \mathrm{[Co(H_2O)_6]^{2+}}</math>
 
the expression for <math>\lambda_{in}</math> can also be derived, but it is more complicated.<ref name = "Sutin"/> These reactions have a free reaction enthalpy <math>\Delta</math>G<sup>0</sup>  which is independent of the reorganization energy and  determined by the different redox potentials of the iron and cobalt couple. Consequently the quadratic Marcus equation holds also for the inner sphere reorganization energy, including the prediction of an inverted region. One may visualizing this by (a) in the normal region both the initial state and the final state have to have stretched bonds, (b) In the <math>\Delta</math> G<math>^\ddagger</math> = 0 case the equilibrium configuration of the initial state is the stretched configuration of the final state, and (c) in the inverted region the initial state has compressed bonds whereas the final state has largely stretched bonds.
Similar considerations hold for metal complexes where the ligands are larger than solvent molecules and also for ligand bridged polynuclear complexes.
 
==The Probability of the Electron Jump==
The strength of the electronic coupling of the donor and acceptor decides whether the electron transfer reaction is adiabatic or non-adiabatic. In the non-adiabatic case the coupling is weak, i.e. H<sub>AB</sub> in Fig. 3 is small compared to the reorganization energy and donor and acceptor retain their identity. The system has a certain probability to jump from the initial to the final potential energy curves. In the adiabatic case the coupling is considerable, the gap of 2 H<sub>AB</sub> is larger and the system stays on the lower potential energy curve.<ref>In normal chemical reactions, like substitutions, which proceed via a transition state the upper potential energy curve is so far up that it is neglected</ref>
 
Marcus theory as laid out above, represents the non-adiabatic case.<ref>The theory of adiabatic electron transfer with participation of nuclear movement (which may be considered as a transfer of charge, not an electron jump), has been worked out by Hush.</ref> Consequently the semi-classical [[Landau-Zener formula|Landau-Zener theory]] can be applied, which gives the probability of interconversion of donor and acceptor for a single passage of the system through the region of the intersection of the potential energy curves
:<math> P_{if} = 1-\exp[-\frac{4\pi^2 {H_{if}^2}}{hv \mid(s_i - s_f)\mid}] </math>
where H<sub>if</sub> is the interaction energy at the intersection, v  the velocity of the system through the intersection region, s<sub>i</sub> and s<sub>f</sub> the slopes there.
[[Image:Parameters of the Marcus Equation.JPG]]
 
Fig. 3 Energy diagram for Electron Transfer including inner and outer sphere reorganization and electronic coupling: The vertical axis is the free energy, and the horizontal axis is the "reaction coordinate" – a simplified axis representing the motion of all the atomic nuclei (inclusive solvent reorganization) 
 
Working this out  one arrives at the basic equation of Marcus theory
 
<math>k_{et} = \frac{2\pi}{\hbar}|H_{AB}|^2 \frac{1}{\sqrt{4\pi \lambda k_bT}}\exp \left ( -\frac{(\lambda +\Delta G^\circ)^2}{4\lambda k_bT} \right )</math>
 
where <math>k_{et}</math> is the rate constant for electron transfer, <math>|H_{AB}|</math> is the electronic coupling between the initial and final states, <math>\lambda</math> is the reorganization energy (both inner and outer-sphere), and <math>\Delta G^\circ</math> is the total [[Gibbs free energy]] change for the electron transfer reaction (<math>k_b</math> is the [[Boltzmann constant]] and <math>T</math> is the [[absolute temperature]]).
 
Thus Marcus's theory builds on the traditional Arrhenius equation for the rates of chemical reactions in two ways:
1. It provides a formula for the activation energy, based on a parameter called the reorganization energy, as well as the Gibbs free energy. The reorganization energy is defined as the energy required to “reorganize” the system structure from initial to final coordinates, without making the charge transfer.
2. It provides a formula for the pre-exponential factor in the Arrhenius equation, based on the electronic coupling between the initial and final state of the electron transfer reaction (i.e., the overlap of the electronic wave functions of the two states).
 
== Experimental Results ==
 
Marcus has published his theory in 1956. For long years there was an intensive search for the inverted region which would be a proof of the theory. But all experiments with series of reactions of more and more negative <math>\Delta</math>G<sup>0</sup> revealed only an increase of  the reaction rate up to the diffusion limit, i.e. to a value indicating that ''every'' encounter lead to electron transfer, and that limit held also for very negative <math>\Delta</math>G<sup>0</sup> values (Rehm-Weller behaviour).<ref>Rehm, D., Weller, A. "Kinetik und Mechanismus der Elektronenübertragung bei der Fluoreszenzlöschung in Acetonitril" ''Ber. Bunsenges.Physik.Chem.'' 1969, '''73''', 834-839 characterized this behaviour by the empirical formula <math> \Delta G^{\ddagger} = \frac{\Delta G^0}{2}+\sqrt{\Delta G^{\ddagger}(0)^2 + \left(\frac{\Delta G^0}{2}\right)^2}  </math></ref> It took about 30 years until the inverted region was unequivocally substantiated by Miller, Calcaterra and Closs for an intermolecular electron transfer in a molecule where donor and acceptor are kept at a constant distance by means of a stiff spacer (Fig.4).<ref>Miller J.R., Calcaterra L.T., Closs G.L.: "Intramolecular long-distance electron transfer in radical anions. The effects of free energy and solvent on the reaction rates", ''J.Am.Chem.Soc.'' 1984, '''106''', 3047, {{DOI|10.1021/ja00322a058}}</ref>
 
[[Image:Marcusparabel MillerCloss.jpg|thumb|Fig.4. Marcus behaviour in a molecule, which is composed of a biphenyl entity, whose anion (produced by means of pulse radiolysis) acts as a donor, a steroid entity, which is a rigid spacer and different aromatic hydrocarbons (1−3) and quinones (4−8), which are the acceptors.<ref>We recommend reference to the original paper, JACS does not license Wikipedia for graphs.</ref>]]
 
''A posteriori'' one may presume that in the systems where the reaction partners may diffuse freely the optimum distance for the electron jump may be sought, i.e. the distance for which <math>\Delta</math>G<sup>‡</sup> = 0 and <math>\Delta</math>G<sup>0</sup> = - <math>\lambda</math><sub>o</sub>. For <math>\lambda</math><sub>o</sub> is dependent on R, <math>\lambda</math><sub>o</sub> increases for larger R and the opening of the parabola smaller. It is formally always possible to close the parabola in Fig. 2 to such an extent, that the f-parabola intersects the i-parabola in the apex. Then always <math>\Delta</math>G<sup>‡</sup> = 0 and the rate k reaches the  maximum diffusional value for all very negative <math>\Delta</math>G<sup>0</sup>. There are, however, other concepts for the phenomenon,<ref name="Nobel"/> e.g. the participation of excited states or that the decrease of the rate constants would be so far in the inverted region that it escapes measurement.
 
R.A. Marcus and his coworkers have further developed the theory outlined here in several aspects. They have included inter alia statistical aspects and quantum effects,<ref>Siders, P.,Marcus, R.A. "Quantum Effects in Electron-Transfer Reactions" ''J.Am.Chem.Soc.'' 1981,'''103''',741; Siders, P., Marcus, R.A. "Quantum Effects for Electron-Transfer Reactions in the 'Inverted Region'" ''J.Am.Chem.Soc.'' 1981,'''103''',748</ref>  they have applied the theory to chemiluminescence <ref>Marcus. R.A. "On the Theory of Chemiluminescent Electron-Transfer Reactions" ''J.Chem.Phys.''1965,'''43''',2654</ref>  and electrode reactions.<ref>Marcus, R.A. "On the theory of Electron-Transfer Reaction IV. Unified Treatment of Homogeneous and Electrode Reactions" ''J.Chem.Phys.'' 1965, '''43'''. 679</ref>  R.A Marcus received the Nobel Prize in Chemistry in 1992, his Nobel Lecture gives an extensive view of his work.<ref name = "Nobel" />
 
==See also==
*[[Hammond's postulate]]
 
== References ==
<references/>
 
==Marcus's Key Papers==
* {{cite journal | author = Marcus, R.A | journal = [[J. Chem. Phys.]] | year = 1956 | volume = 24 | issue = 5 | pages = 966 | doi = 10.1063/1.1742723 | title = On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer. I|bibcode = 1956JChPh..24..966M }}
* {{cite journal | author = Marcus, R.A | journal = [[J. Chem. Phys.]] | year = 1956 | volume = 24 | issue = 5 | pages = 979 | doi = 10.1063/1.1742724 | title = Electrostatic Free Energy and Other Properties of States Having Nonequilibrium Polarization. I|bibcode = 1956JChPh..24..979M }}
* {{cite journal | author = Marcus, R.A | journal = [[J. Chem. Phys.]] | year = 1957 | volume = 26 | issue = 4 | pages = 867 | doi = 10.1063/1.1743423 | title = On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer. II. Applications to Data on the Rates of Isotopic Exchange Reactions|bibcode = 1957JChPh..26..867M }}
* {{cite journal | author = Marcus, R.A | journal = [[J. Chem. Phys.]] | year = 1957 | volume = 26 | issue = 4 | pages = 872 | doi = 10.1063/1.1743424 | title = On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer. III. Applications to Data on the Rates of Organic Redox Reactions|bibcode = 1957JChPh..26..872M }}
* {{cite journal | author = Marcus, R.A | journal = [[Disc. Faraday Soc.]] | year = 1960 | volume = 29 | pages = 21 | doi = 10.1039/df9602900021 | title = Exchange reactions and electron transfer reactions including isotopic exchange. Theory of oxidation-reduction reactions involving electron transfer. Part 4.—A statistical-mechanical basis for treating contributions from solvent, ligands, and inert salt}}
* {{cite journal | author = Marcus, R.A | journal = [[J. Phys. Chem.]] | year = 1963 | volume = 67 | issue = 4 | pages = 853 | doi = 10.1021/j100798a033 | title = On The Theory Of Oxidation--Reduction Reactions Involving Electron Transfer. V. Comparison And Properties Of Electrochemical And Chemical Rate Constants}}
* {{cite journal | author = Marcus, R.A | journal = [[Annu. Rev. Phys. Chem.]] | year = 1964 | volume = 15 | issue = 1 | pages = 155 | doi = 10.1146/annurev.pc.15.100164.001103 | title = Chemical and Electrochemical Electron-Transfer Theory|bibcode = 1964ARPC...15..155M }}
* {{cite journal | author = Marcus, R.A | journal = [[J. Chem. Phys.]] | year = 1965 | volume = 43 | issue = 2 | pages = 679 | doi = 10.1063/1.1696792 | title = On the Theory of Electron-Transfer Reactions. VI. Unified Treatment for Homogeneous and Electrode Reactions|bibcode = 1965JChPh..43..679M }}
* {{cite journal | author = Marcus, R.A.; Sutin N | journal = [[Biochim. Biophys. Acta.]] | year = 1985 | volume = 811 | issue = 3 | pages = 265 | title = Electron transfers in chemistry and biology | doi = 10.1016/0304-4173(85)90014-X}}
 
{{DEFAULTSORT:Marcus Theory}}
[[Category:Physical organic chemistry]]
[[Category:Physical chemistry]]

Revision as of 01:13, 5 October 2013

Marcus Theory is a theory originally developed by Rudolph A. Marcus, starting in 1956, to explain the rates of electron transfer reactions – the rate at which an electron can move or jump from one chemical species (called the electron donor) to another (called the electron acceptor).[1] It was originally formulated to address outer sphere electron transfer reactions, in which the two chemical species only change in their charge with an electron jumping (e.g. the oxidation of an ion like Fe2+/Fe3+), but do not undergo large structural changes. It was extended to include inner sphere electron transfer contributions, in which a change of distances or geometry in the solvation or coordination shells of the two chemical species is taken into account (the Fe-O distances in Fe(H2O)2+ and Fe(H2O)3+ are different).[2][3]

For redox reactions without making or breaking bonds Marcus theory takes the place of Eyring's transition state theory [4][5] which has been derived for reactions with structural changes. Both theories lead to rate equations of the same exponential form. However, whereas in Eyring theory the reaction partners become strongly coupled in the course of the reaction to form a structurally defined activated complex, in Marcus theory they are weakly coupled and retain their individuality. It is the thermally induced reorganization of the surroundings, the solvent (outer sphere) and the solvent sheath or the ligands (inner sphere) which create the geometrically favourable situation prior to and independent of the electron jump.

The original classical Marcus theory for outer sphere electron transfer reactions demonstrates the importance of the solvent and leads the way to the calculation of the Gibbs free energy of activation, using the polarization properties of the solvent, the size of the reactants, the transfer distance and the Gibbs free energy G0 of the redox reaction. The most startling result of Marcus' theory was the "inverted region": whereas the reaction rates usually become higher with increasing exergonicity of the reaction, electron transfer should, according to Marcus theory, become slower in the very negative G0 domain. The inverted region was searched for 30 years until it was unequivocally verified experimentally in 1984.

R.A. Marcus received the Nobel Prize in Chemistry in 1992 for this theory. Marcus theory is used to describe a number of important processes in chemistry and biology, including photosynthesis, corrosion, certain types of chemiluminescence, charge separation in some types of solar cell and more. Besides the inner and outer sphere applications, Marcus theory has been extended to address heterogeneous electron transfer.

The One-Electron Redox Reaction

Chemical reactions may lead to a substitution of a group in a molecule or a ligand in a complex, to the elimination of a group of the molecule or a ligand, or to a rearrangement of a molecule or complex. A chemical reaction may, however, also cause simply an exchange of charges between the reactants, and these redox reactions without making or breaking a bond seem to be quite simple in Inorganic Chemistry for ions and complexes. These reactions often become manifest by a change of colour, e.g. for ions or complexes of transition metal ions, but organic molecules, too, may change their colour by accepting or giving away an electron (like the herbicide Paraquat (4,4'-bipyridyl) which becomes blue when accepting an electron, thence the alternative name of methyl viologen). For this type of redox reactions R.A. Marcus has developed his theory. Here the trace of argument and the results are presented. For the mathematical development and details the original papers[6][7] should be consulted.

In a redox reaction one partner acts as an electron donor D the other as an acceptor A. For a reaction to take place D and A must diffuse together. They form the precursor complex, usually a kinetic, unstable, solvated encounter complex, which by electron transfer is transformed to the successor complex, and finally this separates by diffusion. For a one electron transfer the reaction is

(D and A may already carry charges). Here k12, k21 and k30 are diffusion constants, k23 and k32 rate constants of activated reactions. The total reaction may be diffusion controlled (the electron transfer step is faster than diffusion, every encounter leads to reaction) or activation controlled (the "equilibrium of association" is reached, the electron transfer step is slow, the separation of the successor complex is fast).

Outer Sphere Electron Transfer

Redox reactions are preferably run in polar solvents. Donor and acceptor then have a solvent shell and the precursor and successor complexes are solvated also. The closest molecules of the solvent shell, or the ligands in complexes, are tightly bound and constitute the "inner sphere". Reactions in which these participate are called inner sphere redox reactions. The free solvent molecules constitute the "outer sphere". Outer sphere redox reactions do not change the inner sphere, no bonds are made nor broken.

It was R.A. Marcus who realized the role of the solvent when he worked on the nature and magnitude of the Gibbs free energy of activation for redox reactions, more precisely: one-electron transfer reactions of the outer sphere type. He published two fundamental papers.[6][7] The ideas of these two papers are often referred to Marcus Theory although Marcus’ later work goes much beyond them.[1] In the following the development and results of the ideas of these two papers are outlined. For the mathematics and more details the original papers should be consulted.

The Problem

In outer sphere redox reactions no bonds are formed or broken; only an electron transfer (ET) takes place. A quite simple example is the Fe2+/Fe3+ redox reaction, the self exchange reaction which is known to be always occurring in an aqueous solution containing both FeSO4 and Fe2(SO4)3 (of course, with equal and measurable rates in both directions and with Gibbs free reaction energy G0 = 0).

From the reaction rate's temperature dependence (e.g. the SN2-substitution reaction of the saponification of an alkyl halide) an activation energy is determined, and this activation energy is interpreted as the energy of the transition state in a reaction diagram. The latter is drawn, according to Arrhenius and Eyring, as an energy diagram with the reaction coordinate as the abscissa. The reaction coordinate describes the minimum energy path from the reactants to the products, and the points of this coordinate are combinations of distances and angles between and in the reactants in the course of the formation and/or cleavage of bonds. The maximum of the energy diagram, the transition state, is characterized by a specific configuration of the atoms. Moreover, in Eyring’s TST [4][5] a quite specific change of the nuclear coordinates is responsible for crossing the maximum point, a vibration in this direction is consequently treated as a translation.

For outer sphere redox reactions there cannot be such a reaction path, but nevertheless one does observe an activation energy. The rate equation for activation-controlled reactions has the same exponential form as the Eyring equation,

is the Gibbs free energy of the formation of the transition state, the exponential term represents the probability of its formation, A contains the probability of crossing from precursor to successor complex.

The Marcus Model

The consequence of an electron transfer is the rearrangement of charges, and this gravely influences the solvent environment. For the dipolar solvent molecules rearrange in the direction of the field of the charges (this is called orientation polarisation), and also the atoms and electrons in the solvent molecules are slightly displaced (atomic and electron polarization, respectively). It is this solvent polarization which determines the free energy of activation and thus the reaction rate.

Substitution, elimination and isomerization reactions differ from the outer sphere redox reaction not only in the structural changes outlined above, but also in the fact that the movements of the nuclei and the shift of charges (charge transfer, CT) on the reactions path take place in a continuous and concerted way: nuclear configurations and charge distribution are always “in equilibrium”. This is illustrated by the SN2 substitution of the saponification of an alkyl halide where the rear side attack of the OH- ion pushes out a halide ion and where a transition state with a five-coordinated carbon atom must be visualized. The system of the reactants becomes coupled so tightly during the reaction that they form the activated complex as an integral entity. The solvent here has a minor effect.

By contrast, in outer sphere redox reactions the displacement of nuclei in the reactants are small, here the solvent has the dominant role. Donor-acceptor coupling is weak, both keep their identity during the reaction. Therefore the electron, being an elementary particle, can only “jump” as a whole (electron transfer, ET). If the electron jumps, the transfer is much faster than the movement of the large solvent molecules, with the consequence that the nuclear positions of the reaction partners and the solvent molecules are the same before and after the electron jump (Franck-Condon principle).[8] The jump of the electron is governed by quantum mechanical rules, it is only possible if also the energy of the ET system does not change “during” the jump.

The arrangement of solvent molecules depends on the charge distribution on the reactants. If the solvent configuration must be the same before and after the jump and the energy may not change, then the solvent cannot be in the solvation state of the precursor nor in that of the successor complex as they are different, it has to be somewhere in between. For the self-exchange reaction for symmetry reasons an arrangement of the solvent molecules exactly in the middle of those of precursor and successor complex would meet the conditions. This means that the solvent arrangement with half of the electron on both donor and acceptor would be the correct environment for jumping. Also, in this state the energy of precursor and successor in their solvent environment would be the same.

However, the electron as an elementary particle cannot be divided, it resides either on the donor or the acceptor and arranges the solvent molecules accordingly in an equilibrium. The “transition state”, on the other hand, requires a solvent configuration which would result from the transfer of half an electron, which is impossible. This means that real charge distribution and required solvent polarization are not in an “equilibrium”. Yet it is possible that the solvent takes a configuration corresponding to the “transition state”, even if the electron sits on the donor or acceptor. This, however, requires energy. This energy may be provided by the thermal energy of the solvent and thermal fluctuations can produce the correct polarization state. Once this has been reached the electron can jump. The creation of the correct solvent arrangement and the electron jump are decoupled and do not happen in a synchronous process. Thus the energy of the transition state is mostly polarization energy of the solvent.

Marcus Theory

The Macroscopic System: Two Conducting Spheres

On the basis of his reasoning R.A. Marcus developed a classical theory with the aim of calculating the polarization energy of the said non-equilibrium state. From thermodynamics it is well known that the energy of such a state can be determined if a reversible path to that state is found. Marcus was successful finding such a path via two reversible charging steps for the preparation of the “transition state” from the precursor complex.

Four elements are essential for the model on which the theory is based: (1) Marcus employs a classical, purely electrostatic model. The charge (many elementary charges) may be transferred in any portion from one body to another. (2) Marcus separates the fast electron polarisation Pe and the slow atom and orientation polarisation Pu of the solvent on grounds of their time constants differing several orders of magnitude. (3) Marcus separates the inner sphere (reactant + tightly bound solvent molecules, in complexes + ligands) and the outer sphere (free solvent ) (4) In this model Marcus confines himself to calculating the outer sphere energy of the non-equilibrium polarization of the “transition state”. The outer sphere energy is often much larger than the inner sphere contribution because of the far reaching electrostatic forces (compare the Debye-Hückel theory of electrochemistry).

Marcus’ tool is the theory of dielectric polarization in solvents. He solved the problem in a general way for a transfer of charge between two bodies of arbitrary shape with arbitrary surface and volume charge. For the self-exchange reaction, the redox pair (e.g. Fe(H2O)63+ / Fe(H2O)62+) is substituted by two macroscopic conducting spheres at a defined distance carrying specified charges. Between these spheres a certain amount of charge is reversibly exchanged.

In the first step the energy WI of the transfer of a specific amount of charge is calculated, e.g. for the system in a state when both spheres carry half of the amount of charge which is to be transferred. This state of the system can be reached by transferring the respective charge from the donor sphere to the vacuum and then back to the acceptor sphere.[9] Then the spheres in this state of charge give rise to a defined electric field in the solvent which creates the total solvent polarization Pu + Pe. By the same token this polarization of the solvent interacts with the charges.

In a second step the energy WII of the reversible (back) transfer of the charge to the first sphere, again via the vacuum, is calculated. However, the atom and orientation polarization Pu is kept fixed, only the electron polarization Pe may adjust to the field of the new charge distribution and the fixed Pu. After this second step the system is in the desired state with an electron polarization corresponding to the starting point of the redox reaction and an atom and orientation polarization corresponding to the “transition state”. The energy WI + WII of this state is, thermodynamically speaking, a Gibbs free energy G.

Fig. 1. The parabolas of outer-sphere reorganisation energy of the system two spheres in a solvent. Parabola i: the charge on the first, transfer to the second, parabola f: the charge on the second, transfer to the first. The abscissa is the transferred amount of charge e or the induced polarization P, the ordinate the Gibbs free energy. ΔG(0) = λo/4 is the reorganization energy at Δe = 0.5, it corresponds to the activation energy of the self-exchange reaction.

Of course, in this classical model the transfer any arbitrary amount of charge e is possible. So the energy of the non-equilibrium state, and consequently of the polarization energy of the solvent, can be probed as a function of e. Thus Marcus has lumped together, in a very elegant way, the coordinates of all solvent molecules into a single coordinate of solvent polarization p which is determined by the amount of transferred charge e. So he reached a simplification of the energy representation to only two dimensions: G = f(e). The result for two conducting spheres in a solvent is the formula of Marcus

Where r1 and r2 are the radii of the spheres and R is their separation, s and op are the static and high frequency (optical) dielectric constants of the solvent, e the amount of charge transferred. The graph of G vs. e is a parabola (Fig. 1). In Marcus theory the energy belonging to the transfer of a unit charge (e = 1) is called the (outer sphere) reorganization energy o, i.e. the energy of a state where the polarization would correspond to the transfer of a unit amount of charge, but the real charge distribution is that before the transfer.[10] In terms of exchange direction the system is symmetric.

The Microscopic System: The Redox Pair

Shrinking the two-sphere model to the molecular level creates the problem that in the self exchange reaction the charge can no longer be transferred in arbitrary amounts, but only as a single electron. However, the polarization still is determined by the total ensemble of the solvent molecules and therefore can still be treated classically, i.e. the polarization energy is not subject to quantum limitations. Therefore the energy of solvent reorganization can be calculated as being due to a hypothetical transfer and back transfer of a partial elementary charge according to the Marcus formula. Thus the reorganization energy for chemical redox reactions, which is a Gibbs free energy, is also a parabolic function of e of this hypothetical transfer, For the self exchange reaction, where for symmetry reasons e = 0.5, the Gibbs free energy of activation is G(0) = o/4 (see Fig. 1 and Fig.2 intersection of the parabolas I and f, f(0), respectively).

Up to now all was physics, now some chemistry enters. The self exchange reaction is a very specific redox reaction, most of the redox reactions are between different partners [11] e.g.

and they have positive (endergonic) or negative (exergonic) Gibbs free energies of reaction G0.

As Marcus calculations refer exclusively to the electrostatic properties in the solvent (outer sphere) G0 and o are independent of one another and therefore can just be added up. This means that the Marcus parabolas in systems with different G0 are shifted just up or down in the G vs. e diagram (Fig. 2). Variation of G0 can be affected in experiments by offering different acceptors to the same donor.

Simple calculations of the points of intersection of the parabolas i (y = x2), f(0) (y = (x-d)2) and f1 to f3 (y = (x-d)2 +c) give the Gibbs free energy of activation

It should be noted that the intersection of those parabolas represents an activation energy and not the energy of a transition state of fixed configuration of all nuclei in the system as is the case in the substitution and other reactions mentioned. The transition state of the latter reactions has to meet structural and energetic conditions, redox reactions have only to comply to the energy requirement. Whereas the geometry of the transition state in the other reactions is the same for all pairs of reactants, for redox pairs many polarization environments may meet the energetic conditions.

Fig. 2 Marcus-Parabolas for different redox reactions: f1 such with positive ΔG0, f(0) for the self-exchange reaction with ΔG0 = 0 (broken line), f2 for moderately negative ΔG0 (selected so, that ΔG = 0) and f3 for strongly negative ΔG0. The free energy of activation ΔG decreases from f1 (b1) via f(0) (a) to f2 (zero) and increases again for f3 („Marcus inverted region“).

Marcus’ formula shows a quadratic dependence of the Gibbs free energy of activation on the Gibbs free energy of reaction. It is general knowledge from the host of chemical experience that reactions usually are the faster the more negative is G0. In many cases even a linear free energy relation is found. According to the Marcus formula the rates increase also when the reactions are more exergonic, however only as long as G0 is positive or slightly negative. It is surprising that for redox reactions according to the Marcus formula the activation energy should increase for very exergonic reaction, i.e. in the cases when G0is negative and its absolute value is greater than that of o. This realm of Gibbs free energy of reaction is called “Marcus inverted region”. In Fig. 2 it becomes obvious that the intersection of the parabolas i and f moves upwards in the left part of the graph when G0 continues to become more negative, and this means increasing activation energy. Thus the total graph of ln k vs. G0 should have a maximum.

The maximum of the ET rate is expected at G = 0. Here e = 0 and q = 0 (Abb.2) which means that the electron may jump in the precursor complex at its equilibrium polarization. No thermal activation is necessary: the reaction is barrierless. In the inverted region the polarization corresponds to the difficult to imagine notion of a charge distribution where the donor has received and the acceptor given off charge. Of course, in real world this does not happen, it is not a real charge distribution which creates this critical polarization, but the thermal fluctuation in the solvent. This polarization necessary for transfer in the inverted region can be created – with some probability – as well as any other one.[12] The electron is just waiting for it for jumping.

Inner Sphere Electron Transfer

In the outer sphere model the donor or acceptor and the tightly bound solvation shells or the complex’ ligands were considered to form rigid structures which do not change in the course of electron transfer. However, the distances in the inner sphere are dependent on the charge of donor and acceptor, e.g. the central ion-ligand distances are different in complexes carrying different charges And again the Franck-Condon principle must be obeyed: for the electron to jump to occur, the nuclei have to have a configuration which is an identical one of as well the precursor as the successor complexes, of course highly distorted. In this case the energy requirement is fulfilled automatically.

In this inner sphere case the Arrhenius concept holds, the transition state of definite geometric structure is reached along a geometrical reaction coordinate determined by nuclear motions. No further nuclear motion is necessary to form the successor complex, just the electron jumps, which makes a difference to the TST theory. The reaction coordinate for inner sphere energy is governed by vibrations and they differ in the oxidized and reduces species.[13]

For the self-exchange system Fe2+/Fe3+ only the symmetrical breathing vibration of the six water molecules around the iron ions is considered.[13] Assuming harmonic conditions this vibration has frequencies and , the force constants fD and fA are and the energies are

where q0 is the equilibrium normal coordinate and the displacement along the normal coordinate, the factor 3 stems from 6 (H2O) ½. Like for the outer-sphere reorganization energy potential energy curve is quadratic, here, however, as a consequence of vibrations.

The equilibrium normal coordinates differ in Fe(H2O)62+ and Fe(H2O)63+. By thermal excitation of the breathing vibration a geometry can be reached which is common to both donor and acceptor, i.e. the potential energy curves of the breathing vibrations of D and A intersect here. This is the situation where the electron may jump. The energy of this transition state is the inner sphere reorganization energy in.

For the self-exchange reaction the metal-water distance in the transition state can be calculated [13]

This gives the inner sphere reorganisation energy

It is fortunate that the expressions for the energies for outer and inner reorganization have the same quadratic form. Inner sphere and outer sphere reorganization energies are independent, so they can be added to give and inserted in the Arrhenius equation

Here, A can be seen to represent the probability of electron jump, exp[-Gin/kT] that of reaching the transition state of the inner sphere and exp[-Go/kT] that of outer sphere adjustment . For unsymmetrical (cross) reactions like

the expression for can also be derived, but it is more complicated.[13] These reactions have a free reaction enthalpy G0 which is independent of the reorganization energy and determined by the different redox potentials of the iron and cobalt couple. Consequently the quadratic Marcus equation holds also for the inner sphere reorganization energy, including the prediction of an inverted region. One may visualizing this by (a) in the normal region both the initial state and the final state have to have stretched bonds, (b) In the G = 0 case the equilibrium configuration of the initial state is the stretched configuration of the final state, and (c) in the inverted region the initial state has compressed bonds whereas the final state has largely stretched bonds. Similar considerations hold for metal complexes where the ligands are larger than solvent molecules and also for ligand bridged polynuclear complexes.

The Probability of the Electron Jump

The strength of the electronic coupling of the donor and acceptor decides whether the electron transfer reaction is adiabatic or non-adiabatic. In the non-adiabatic case the coupling is weak, i.e. HAB in Fig. 3 is small compared to the reorganization energy and donor and acceptor retain their identity. The system has a certain probability to jump from the initial to the final potential energy curves. In the adiabatic case the coupling is considerable, the gap of 2 HAB is larger and the system stays on the lower potential energy curve.[14]

Marcus theory as laid out above, represents the non-adiabatic case.[15] Consequently the semi-classical Landau-Zener theory can be applied, which gives the probability of interconversion of donor and acceptor for a single passage of the system through the region of the intersection of the potential energy curves

where Hif is the interaction energy at the intersection, v the velocity of the system through the intersection region, si and sf the slopes there.


Fig. 3 Energy diagram for Electron Transfer including inner and outer sphere reorganization and electronic coupling: The vertical axis is the free energy, and the horizontal axis is the "reaction coordinate" – a simplified axis representing the motion of all the atomic nuclei (inclusive solvent reorganization)

Working this out one arrives at the basic equation of Marcus theory

where is the rate constant for electron transfer, is the electronic coupling between the initial and final states, is the reorganization energy (both inner and outer-sphere), and is the total Gibbs free energy change for the electron transfer reaction ( is the Boltzmann constant and is the absolute temperature).

Thus Marcus's theory builds on the traditional Arrhenius equation for the rates of chemical reactions in two ways: 1. It provides a formula for the activation energy, based on a parameter called the reorganization energy, as well as the Gibbs free energy. The reorganization energy is defined as the energy required to “reorganize” the system structure from initial to final coordinates, without making the charge transfer. 2. It provides a formula for the pre-exponential factor in the Arrhenius equation, based on the electronic coupling between the initial and final state of the electron transfer reaction (i.e., the overlap of the electronic wave functions of the two states).

Experimental Results

Marcus has published his theory in 1956. For long years there was an intensive search for the inverted region which would be a proof of the theory. But all experiments with series of reactions of more and more negative G0 revealed only an increase of the reaction rate up to the diffusion limit, i.e. to a value indicating that every encounter lead to electron transfer, and that limit held also for very negative G0 values (Rehm-Weller behaviour).[16] It took about 30 years until the inverted region was unequivocally substantiated by Miller, Calcaterra and Closs for an intermolecular electron transfer in a molecule where donor and acceptor are kept at a constant distance by means of a stiff spacer (Fig.4).[17]

Fig.4. Marcus behaviour in a molecule, which is composed of a biphenyl entity, whose anion (produced by means of pulse radiolysis) acts as a donor, a steroid entity, which is a rigid spacer and different aromatic hydrocarbons (1−3) and quinones (4−8), which are the acceptors.[18]

A posteriori one may presume that in the systems where the reaction partners may diffuse freely the optimum distance for the electron jump may be sought, i.e. the distance for which G = 0 and G0 = - o. For o is dependent on R, o increases for larger R and the opening of the parabola smaller. It is formally always possible to close the parabola in Fig. 2 to such an extent, that the f-parabola intersects the i-parabola in the apex. Then always G = 0 and the rate k reaches the maximum diffusional value for all very negative G0. There are, however, other concepts for the phenomenon,[1] e.g. the participation of excited states or that the decrease of the rate constants would be so far in the inverted region that it escapes measurement.

R.A. Marcus and his coworkers have further developed the theory outlined here in several aspects. They have included inter alia statistical aspects and quantum effects,[19] they have applied the theory to chemiluminescence [20] and electrode reactions.[21] R.A Marcus received the Nobel Prize in Chemistry in 1992, his Nobel Lecture gives an extensive view of his work.[1]

See also

References

  1. 1.0 1.1 1.2 1.3 Template:Internetquelle
  2. Contrary to Marcus' approach the inner sphere electron transfer theory of Noel S. Hush refers to a continuous change of the electron density during transfer along a geometrical coordinate (adiabatic case), and takes also into account the solvent influence as did Marcus. Hush's formulation is known as Marcus-Hush theory.
  3. Hush, N.S. Trans. Faraday Soc. 1961, 57,557
  4. 4.0 4.1 P. W. Atkins: Physical Chemistry, 6. Ed., Oxford University Press, Oxford 1998 p.830
  5. 5.0 5.1 R.S. Berry, S. A. Rice, J. Ross: Physical Chemistry, Wiley, New York 1980, S. 1147 ff,
  6. 6.0 6.1 Marcus, R.A. "On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer I" J.Chem.Phys.1956, 24, 966. Electronic Instrument Positions Staff (Standard ) Cameron from Clarence Creek, usually spends time with hobbies and interests which include knotting, property developers in singapore apartment For sale and boomerangs. Has enrolled in a world contiki journey. Is extremely thrilled specifically about visiting . or Free Text
  7. 7.0 7.1 Marcus.R.A. "Electrostatic Free Energy and Other Properties of States Having Nonequilibrium Polarization I. J.Chem.Phys.1956, 24, 979. Electronic Instrument Positions Staff (Standard ) Cameron from Clarence Creek, usually spends time with hobbies and interests which include knotting, property developers in singapore apartment For sale and boomerangs. Has enrolled in a world contiki journey. Is extremely thrilled specifically about visiting . or Free Text
  8. W.F. Libby, "Theory of Electron Exchange Reactions in Aquous Solution" J.Phys.Chem. 1952, 56, 863
  9. Marcus takes the vacuum state of the reactants as the zero energy point. Therefore many of his equations contain also the solvation energy of the isolated species Wiso and the electrostatic energy of formation of the precursor and successor complexes.
  10. Note: The quadratic dependence of outer sphere reorganization energy is not a consequence of vibrations in reactants or solvent!
  11. they are often called Marcus cross reactions.
  12. The reverse reaction may support understanding: for this reaction the polarization due to the hypothetical transfer of a unit electron charge is not sufficient to reach a polarization where the polarization energies of A/D and A-/D+ are equal. This can only happen on the hypothetical transfer of more that one electron charge.
  13. 13.0 13.1 13.2 13.3 N. Sutin, 'Theory of Electron Transfer Reactions: Insights and Hindsights', Progr. Inorg. Chem. 1083, 30, 441-448
  14. In normal chemical reactions, like substitutions, which proceed via a transition state the upper potential energy curve is so far up that it is neglected
  15. The theory of adiabatic electron transfer with participation of nuclear movement (which may be considered as a transfer of charge, not an electron jump), has been worked out by Hush.
  16. Rehm, D., Weller, A. "Kinetik und Mechanismus der Elektronenübertragung bei der Fluoreszenzlöschung in Acetonitril" Ber. Bunsenges.Physik.Chem. 1969, 73, 834-839 characterized this behaviour by the empirical formula
  17. Miller J.R., Calcaterra L.T., Closs G.L.: "Intramolecular long-distance electron transfer in radical anions. The effects of free energy and solvent on the reaction rates", J.Am.Chem.Soc. 1984, 106, 3047, Electronic Instrument Positions Staff (Standard ) Cameron from Clarence Creek, usually spends time with hobbies and interests which include knotting, property developers in singapore apartment For sale and boomerangs. Has enrolled in a world contiki journey. Is extremely thrilled specifically about visiting .
  18. We recommend reference to the original paper, JACS does not license Wikipedia for graphs.
  19. Siders, P.,Marcus, R.A. "Quantum Effects in Electron-Transfer Reactions" J.Am.Chem.Soc. 1981,103,741; Siders, P., Marcus, R.A. "Quantum Effects for Electron-Transfer Reactions in the 'Inverted Region'" J.Am.Chem.Soc. 1981,103,748
  20. Marcus. R.A. "On the Theory of Chemiluminescent Electron-Transfer Reactions" J.Chem.Phys.1965,43,2654
  21. Marcus, R.A. "On the theory of Electron-Transfer Reaction IV. Unified Treatment of Homogeneous and Electrode Reactions" J.Chem.Phys. 1965, 43. 679

Marcus's Key Papers

  • One of the biggest reasons investing in a Singapore new launch is an effective things is as a result of it is doable to be lent massive quantities of money at very low interest rates that you should utilize to purchase it. Then, if property values continue to go up, then you'll get a really high return on funding (ROI). Simply make sure you purchase one of the higher properties, reminiscent of the ones at Fernvale the Riverbank or any Singapore landed property Get Earnings by means of Renting

    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

    A vendor's stamp duty has been launched on industrial property for the primary time, at rates ranging from 5 per cent to 15 per cent. The Authorities might be trying to reassure the market that they aren't in opposition to foreigners and PRs investing in Singapore's property market. They imposed these measures because of extenuating components available in the market." The sale of new dual-key EC models will even be restricted to multi-generational households only. The models have two separate entrances, permitting grandparents, for example, to dwell separately. The vendor's stamp obligation takes effect right this moment and applies to industrial property and plots which might be offered inside three years of the date of buy. JLL named Best Performing Property Brand for second year running

    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

    There are various methods to go about discovering the precise property. Some local newspapers (together with the Straits Instances ) have categorised property sections and many local property brokers have websites. Now there are some specifics to consider when buying a 'new launch' rental. Intended use of the unit Every sale begins with 10 p.c low cost for finish of season sale; changes to 20 % discount storewide; follows by additional reduction of fiftyand ends with last discount of 70 % or extra. Typically there is even a warehouse sale or transferring out sale with huge mark-down of costs for stock clearance. Deborah Regulation from Expat Realtor shares her property market update, plus prime rental residences and houses at the moment available to lease Esparina EC @ Sengkang
  • One of the biggest reasons investing in a Singapore new launch is an effective things is as a result of it is doable to be lent massive quantities of money at very low interest rates that you should utilize to purchase it. Then, if property values continue to go up, then you'll get a really high return on funding (ROI). Simply make sure you purchase one of the higher properties, reminiscent of the ones at Fernvale the Riverbank or any Singapore landed property Get Earnings by means of Renting

    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

    A vendor's stamp duty has been launched on industrial property for the primary time, at rates ranging from 5 per cent to 15 per cent. The Authorities might be trying to reassure the market that they aren't in opposition to foreigners and PRs investing in Singapore's property market. They imposed these measures because of extenuating components available in the market." The sale of new dual-key EC models will even be restricted to multi-generational households only. The models have two separate entrances, permitting grandparents, for example, to dwell separately. The vendor's stamp obligation takes effect right this moment and applies to industrial property and plots which might be offered inside three years of the date of buy. JLL named Best Performing Property Brand for second year running

    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

    There are various methods to go about discovering the precise property. Some local newspapers (together with the Straits Instances ) have categorised property sections and many local property brokers have websites. Now there are some specifics to consider when buying a 'new launch' rental. Intended use of the unit Every sale begins with 10 p.c low cost for finish of season sale; changes to 20 % discount storewide; follows by additional reduction of fiftyand ends with last discount of 70 % or extra. Typically there is even a warehouse sale or transferring out sale with huge mark-down of costs for stock clearance. Deborah Regulation from Expat Realtor shares her property market update, plus prime rental residences and houses at the moment available to lease Esparina EC @ Sengkang
  • One of the biggest reasons investing in a Singapore new launch is an effective things is as a result of it is doable to be lent massive quantities of money at very low interest rates that you should utilize to purchase it. Then, if property values continue to go up, then you'll get a really high return on funding (ROI). Simply make sure you purchase one of the higher properties, reminiscent of the ones at Fernvale the Riverbank or any Singapore landed property Get Earnings by means of Renting

    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

    A vendor's stamp duty has been launched on industrial property for the primary time, at rates ranging from 5 per cent to 15 per cent. The Authorities might be trying to reassure the market that they aren't in opposition to foreigners and PRs investing in Singapore's property market. They imposed these measures because of extenuating components available in the market." The sale of new dual-key EC models will even be restricted to multi-generational households only. The models have two separate entrances, permitting grandparents, for example, to dwell separately. The vendor's stamp obligation takes effect right this moment and applies to industrial property and plots which might be offered inside three years of the date of buy. JLL named Best Performing Property Brand for second year running

    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

    There are various methods to go about discovering the precise property. Some local newspapers (together with the Straits Instances ) have categorised property sections and many local property brokers have websites. Now there are some specifics to consider when buying a 'new launch' rental. Intended use of the unit Every sale begins with 10 p.c low cost for finish of season sale; changes to 20 % discount storewide; follows by additional reduction of fiftyand ends with last discount of 70 % or extra. Typically there is even a warehouse sale or transferring out sale with huge mark-down of costs for stock clearance. Deborah Regulation from Expat Realtor shares her property market update, plus prime rental residences and houses at the moment available to lease Esparina EC @ Sengkang
  • One of the biggest reasons investing in a Singapore new launch is an effective things is as a result of it is doable to be lent massive quantities of money at very low interest rates that you should utilize to purchase it. Then, if property values continue to go up, then you'll get a really high return on funding (ROI). Simply make sure you purchase one of the higher properties, reminiscent of the ones at Fernvale the Riverbank or any Singapore landed property Get Earnings by means of Renting

    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

    A vendor's stamp duty has been launched on industrial property for the primary time, at rates ranging from 5 per cent to 15 per cent. The Authorities might be trying to reassure the market that they aren't in opposition to foreigners and PRs investing in Singapore's property market. They imposed these measures because of extenuating components available in the market." The sale of new dual-key EC models will even be restricted to multi-generational households only. The models have two separate entrances, permitting grandparents, for example, to dwell separately. The vendor's stamp obligation takes effect right this moment and applies to industrial property and plots which might be offered inside three years of the date of buy. JLL named Best Performing Property Brand for second year running

    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

    There are various methods to go about discovering the precise property. Some local newspapers (together with the Straits Instances ) have categorised property sections and many local property brokers have websites. Now there are some specifics to consider when buying a 'new launch' rental. Intended use of the unit Every sale begins with 10 p.c low cost for finish of season sale; changes to 20 % discount storewide; follows by additional reduction of fiftyand ends with last discount of 70 % or extra. Typically there is even a warehouse sale or transferring out sale with huge mark-down of costs for stock clearance. Deborah Regulation from Expat Realtor shares her property market update, plus prime rental residences and houses at the moment available to lease Esparina EC @ Sengkang
  • One of the biggest reasons investing in a Singapore new launch is an effective things is as a result of it is doable to be lent massive quantities of money at very low interest rates that you should utilize to purchase it. Then, if property values continue to go up, then you'll get a really high return on funding (ROI). Simply make sure you purchase one of the higher properties, reminiscent of the ones at Fernvale the Riverbank or any Singapore landed property Get Earnings by means of Renting

    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

    A vendor's stamp duty has been launched on industrial property for the primary time, at rates ranging from 5 per cent to 15 per cent. The Authorities might be trying to reassure the market that they aren't in opposition to foreigners and PRs investing in Singapore's property market. They imposed these measures because of extenuating components available in the market." The sale of new dual-key EC models will even be restricted to multi-generational households only. The models have two separate entrances, permitting grandparents, for example, to dwell separately. The vendor's stamp obligation takes effect right this moment and applies to industrial property and plots which might be offered inside three years of the date of buy. JLL named Best Performing Property Brand for second year running

    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

    There are various methods to go about discovering the precise property. Some local newspapers (together with the Straits Instances ) have categorised property sections and many local property brokers have websites. Now there are some specifics to consider when buying a 'new launch' rental. Intended use of the unit Every sale begins with 10 p.c low cost for finish of season sale; changes to 20 % discount storewide; follows by additional reduction of fiftyand ends with last discount of 70 % or extra. Typically there is even a warehouse sale or transferring out sale with huge mark-down of costs for stock clearance. Deborah Regulation from Expat Realtor shares her property market update, plus prime rental residences and houses at the moment available to lease Esparina EC @ Sengkang
  • One of the biggest reasons investing in a Singapore new launch is an effective things is as a result of it is doable to be lent massive quantities of money at very low interest rates that you should utilize to purchase it. Then, if property values continue to go up, then you'll get a really high return on funding (ROI). Simply make sure you purchase one of the higher properties, reminiscent of the ones at Fernvale the Riverbank or any Singapore landed property Get Earnings by means of Renting

    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

    A vendor's stamp duty has been launched on industrial property for the primary time, at rates ranging from 5 per cent to 15 per cent. The Authorities might be trying to reassure the market that they aren't in opposition to foreigners and PRs investing in Singapore's property market. They imposed these measures because of extenuating components available in the market." The sale of new dual-key EC models will even be restricted to multi-generational households only. The models have two separate entrances, permitting grandparents, for example, to dwell separately. The vendor's stamp obligation takes effect right this moment and applies to industrial property and plots which might be offered inside three years of the date of buy. JLL named Best Performing Property Brand for second year running

    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

    There are various methods to go about discovering the precise property. Some local newspapers (together with the Straits Instances ) have categorised property sections and many local property brokers have websites. Now there are some specifics to consider when buying a 'new launch' rental. Intended use of the unit Every sale begins with 10 p.c low cost for finish of season sale; changes to 20 % discount storewide; follows by additional reduction of fiftyand ends with last discount of 70 % or extra. Typically there is even a warehouse sale or transferring out sale with huge mark-down of costs for stock clearance. Deborah Regulation from Expat Realtor shares her property market update, plus prime rental residences and houses at the moment available to lease Esparina EC @ Sengkang
  • One of the biggest reasons investing in a Singapore new launch is an effective things is as a result of it is doable to be lent massive quantities of money at very low interest rates that you should utilize to purchase it. Then, if property values continue to go up, then you'll get a really high return on funding (ROI). Simply make sure you purchase one of the higher properties, reminiscent of the ones at Fernvale the Riverbank or any Singapore landed property Get Earnings by means of Renting

    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

    A vendor's stamp duty has been launched on industrial property for the primary time, at rates ranging from 5 per cent to 15 per cent. The Authorities might be trying to reassure the market that they aren't in opposition to foreigners and PRs investing in Singapore's property market. They imposed these measures because of extenuating components available in the market." The sale of new dual-key EC models will even be restricted to multi-generational households only. The models have two separate entrances, permitting grandparents, for example, to dwell separately. The vendor's stamp obligation takes effect right this moment and applies to industrial property and plots which might be offered inside three years of the date of buy. JLL named Best Performing Property Brand for second year running

    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

    There are various methods to go about discovering the precise property. Some local newspapers (together with the Straits Instances ) have categorised property sections and many local property brokers have websites. Now there are some specifics to consider when buying a 'new launch' rental. Intended use of the unit Every sale begins with 10 p.c low cost for finish of season sale; changes to 20 % discount storewide; follows by additional reduction of fiftyand ends with last discount of 70 % or extra. Typically there is even a warehouse sale or transferring out sale with huge mark-down of costs for stock clearance. Deborah Regulation from Expat Realtor shares her property market update, plus prime rental residences and houses at the moment available to lease Esparina EC @ Sengkang
  • One of the biggest reasons investing in a Singapore new launch is an effective things is as a result of it is doable to be lent massive quantities of money at very low interest rates that you should utilize to purchase it. Then, if property values continue to go up, then you'll get a really high return on funding (ROI). Simply make sure you purchase one of the higher properties, reminiscent of the ones at Fernvale the Riverbank or any Singapore landed property Get Earnings by means of Renting

    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

    A vendor's stamp duty has been launched on industrial property for the primary time, at rates ranging from 5 per cent to 15 per cent. The Authorities might be trying to reassure the market that they aren't in opposition to foreigners and PRs investing in Singapore's property market. They imposed these measures because of extenuating components available in the market." The sale of new dual-key EC models will even be restricted to multi-generational households only. The models have two separate entrances, permitting grandparents, for example, to dwell separately. The vendor's stamp obligation takes effect right this moment and applies to industrial property and plots which might be offered inside three years of the date of buy. JLL named Best Performing Property Brand for second year running

    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

    There are various methods to go about discovering the precise property. Some local newspapers (together with the Straits Instances ) have categorised property sections and many local property brokers have websites. Now there are some specifics to consider when buying a 'new launch' rental. Intended use of the unit Every sale begins with 10 p.c low cost for finish of season sale; changes to 20 % discount storewide; follows by additional reduction of fiftyand ends with last discount of 70 % or extra. Typically there is even a warehouse sale or transferring out sale with huge mark-down of costs for stock clearance. Deborah Regulation from Expat Realtor shares her property market update, plus prime rental residences and houses at the moment available to lease Esparina EC @ Sengkang
  • One of the biggest reasons investing in a Singapore new launch is an effective things is as a result of it is doable to be lent massive quantities of money at very low interest rates that you should utilize to purchase it. Then, if property values continue to go up, then you'll get a really high return on funding (ROI). Simply make sure you purchase one of the higher properties, reminiscent of the ones at Fernvale the Riverbank or any Singapore landed property Get Earnings by means of Renting

    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

    A vendor's stamp duty has been launched on industrial property for the primary time, at rates ranging from 5 per cent to 15 per cent. The Authorities might be trying to reassure the market that they aren't in opposition to foreigners and PRs investing in Singapore's property market. They imposed these measures because of extenuating components available in the market." The sale of new dual-key EC models will even be restricted to multi-generational households only. The models have two separate entrances, permitting grandparents, for example, to dwell separately. The vendor's stamp obligation takes effect right this moment and applies to industrial property and plots which might be offered inside three years of the date of buy. JLL named Best Performing Property Brand for second year running

    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

    There are various methods to go about discovering the precise property. Some local newspapers (together with the Straits Instances ) have categorised property sections and many local property brokers have websites. Now there are some specifics to consider when buying a 'new launch' rental. Intended use of the unit Every sale begins with 10 p.c low cost for finish of season sale; changes to 20 % discount storewide; follows by additional reduction of fiftyand ends with last discount of 70 % or extra. Typically there is even a warehouse sale or transferring out sale with huge mark-down of costs for stock clearance. Deborah Regulation from Expat Realtor shares her property market update, plus prime rental residences and houses at the moment available to lease Esparina EC @ Sengkang