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{{Coupling in molecules}}
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'''Vibronic coupling''', nonadiabatic coupling or derivative coupling in a [[molecule]] involves the interaction between electronic and nuclear vibrational motion.<ref name=encyclopedia>{{cite book|chapter=Nonadiabatic Derivative Couplings|last=Yarkony|first=David R|editor-last=Paul von Ragué Schleyer et al|title=Encyclopedia of Computational Chemistry|year=1998|publisher=Wiley|location=Chichester|isbn=0-471-96588-X|url=http://onlinelibrary.wiley.com/doi/10.1002/0470845015.cna007/abstract}}</ref><ref>{{ cite journal|doi=10.1111/j.1751-1097.1977.tb06918.x |first=T. |last=Azumi|title=WHAT DOES THE TERM "VIBRONIC COUPLING" MEAN?|journal= Photochemistry and Photobiology|volume= 25| pages=315–326|year=1977}}</ref>  The term "vibronic" originates from the combination of the terms "vibrational" and "electronic". The word coupling denotes the idea that in a molecule, vibrational and electronic interactions are interrelated and influence each other, and the magnitude of vibronic coupling reflects the degree of such interrelation.  
 
In [[theoretical chemistry]], the vibronic coupling is neglected within the [[Born&ndash;Oppenheimer approximation]].   Vibronic couplings are crucial to the understanding of nonadiabatic processes, especially near points of [[conical intersection]]s.<ref>{{cite journal|last=Yarkony|first=David R.|title=Nonadiabatic Quantum Chemistry—Past, Present, and Future|journal=Chemical Reviews|date=11 January 2012|volume=112|issue=1|pages=481–498|doi=10.1021/cr2001299}}</ref><ref>{{cite book|last=Baer|first=Michael|title=Beyond Born-Oppenheimer : electronic non-adiabatic coupling terms and conical intersections|year=2006|publisher=Wiley|location=Hoboken, N.J.|isbn=0471778915}}</ref>  The direct calculation of vibronic couplings is not common due to difficulties associated with its evaluation.
 
== Definition ==
Vibronic coupling describes the mixing of different electronic state as a result of small vibrations.
:<math>
\mathbf{f}_{k' k}\equiv\langle\,\chi_{k'}(\mathbf{r};\mathbf{R})\,|\, \hat{\nabla}_\mathbf{R}\chi_k(\mathbf{r};\mathbf{R})\rangle_{(\mathbf{r})}
</math>
 
== Evaluation ==
The evaluation of vibronic coupling often involve complex mathematical treatment.
 
=== Numerical Gradients ===
The form of vibronic coupling is essentially derivative of the [[wave function]].  Each component of the vibronic coupling vector can be calculated with [[numerical differentiation]] methods using [[wave function]]s at displaced geometries.   This is the procedure used in [[MOLPRO]].<ref name=MOLPRO>{{cite web|title=NON ADIABATIC COUPLING MATRIX ELEMENTS|url=http://www.molpro.net/info/2012.1/doc/manual/node509.html|publisher=MOLPRO|accessdate=3 November 2012}}</ref>
 
First order accuracy can be achieved with forward difference formula:
 
:<math>
(\mathbf{f}_{k' k})_l\approx\frac{1}{d}\left[\gamma^{k' k}(\mathbf{R}|\mathbf{R}+d\mathbf{e}_l)-\gamma^{k' k}(\mathbf{R}|\mathbf{R})\right]
</math>
 
Second order accuracy can be achieved with central difference formula:
 
:<math>
(\mathbf{f}_{k' k})_l\approx\frac{1}{2d}\left[\gamma^{k' k}(\mathbf{R}|\mathbf{R}+d\mathbf{e}_l)-\gamma^{k' k}(\mathbf{R}|\mathbf{R}-d\mathbf{e}_l)\right]
</math>
 
Here, <math>\mathbf{e}_l</math> is a unit vector along direction <math>l</math>. <math>\gamma^{k' k}</math> is the transition density between the two electronic states.
 
:<math>
\gamma^{k' k}(\mathbf{R}_1|\mathbf{R}_2)=\langle\chi_{k'}(\mathbf{r};\mathbf{R}_1)\,|\,\chi_k(\mathbf{r};\mathbf{R}_2)\rangle_{(\mathbf{r})}
</math>
 
Evaluation of electronic wave functions for both electronic states are required at N displacement geometries for first order accuracy and 2*N displacements to achieve second order accuracy, where N is the number of nuclear degrees of freedom. This can be very expensive for larger molecules.
 
As with other numerical differentiation method, the evaluation of nonadiabatic coupling vector with this method is numerically unstable, limiting the accuracy of the result.  Moreover, the calculation of the two transition densities in the numerator are not straightforward. The wave functions of both electronic states are expanded with [[Slater determinants]] or [[Configuration state function]]s(CSF).  The contribution form the change of CSF basis is too expensive to evaluate using numerical method, and is usually ignored by employing an approximate [[diabatic]] CSF basis. This will also cause further inaccuracy of the calculated coupling vector, although the error is usually tolerable.
 
=== Analytic Gradient Methods ===
Evaluating derivative couplings with analytic gradient methods has the advantage of high accuracy and very low cost, usually much cheaper than one single point calculation. This means an acceleration factor of 2N.  However, the process involves intense mathematical  treatment and programming.  As a result, few programs have currently implemented analytic evaluation of vibronic couplings. Details about this method can be found in ref.<ref>{{cite journal|last=Lengsfield|first=Byron H.|coauthors=Saxe, Paul; Yarkony, David R.|title=On the evaluation of nonadiabatic coupling matrix elements using SA-MCSCF/CI wave functions and analytic gradient methods. I|journal=The Journal of Chemical Physics|date=1 January 1984|volume=81|issue=10|pages=4549|doi=10.1063/1.447428|bibcode = 1984JChPh..81.4549L }}</ref>   For the implementation for SA-MCSCF and [[MRCI]] in [[COLUMBUS]] please see ref.<ref>{{cite journal|last=Lischka|first=Hans|coauthors=Dallos, Michal; Szalay, Péter G.; Yarkony, David R.; Shepard, Ron|title=Analytic evaluation of nonadiabatic coupling terms at the MR-CI level. I. Formalism|journal=The Journal of Chemical Physics|date=1 January 2004|volume=120|issue=16|pages=7322|doi=10.1063/1.1668615|bibcode = 2004JChPh.120.7322L }}</ref>
 
==Crossings and avoided crossings of potential energy surfaces==
{{Main|Potential energy surface|Conical intersection}}
Vibronic coupling is large in the case of two [[adiabatic]] [[potential energy surface]]s coming close to each other (that is, when the energy gap between them is of the order of magnitude of one oscillation quantum).  This happens in the neighbourhood of an [[avoided crossing]] of  [[potential energy surface]]s corresponding to distinct electronic states of the same spin symmetry. At the vicinity of [[conical intersection]]s, where the potential energy surfaces of the same spin symmetry cross, the magnitude of vibronic coupling approaches infinity. In either case the [[adiabatic process (quantum mechanics)|adiabatic]] or [[Born&ndash;Oppenheimer approximation]] fails and vibronic couplings have to be taken into account. 
 
The large magnitude of vibronic coupling near [[avoided crossing]]s and [[conical intersection]]s allows wavefunctions to propagate from one adiabatic potential energy surface to another, giving rise to nonadiabatic phenomena such as [[Quenching (fluorescence)|radiationless decay]].   The singularity of vibronic coupling at conical intersections is responsible for the existence of [[Berry phase]], which has been discovered by [[H. Christopher Longuet-Higgins|Longuet-Higgins]] in this context.
 
==Difficulties and alternatives==
Although crucial to the understanding of nonadiabatic processes, direct evaluation of vibronic couplings has been very limited.
 
Evaluation of vibronic couplings is often associated with severe difficulties in mathematical formulation and program implementations.  As a result, the algorithms to evaluate vibronic couplings are not yet implemented in many [[quantum chemistry]] program suites.  
 
The evaluation of vibronic couplings also requires correct description of at least two electronic states in regions where they are strongly coupled. This requires the use of multi-reference methods such as [[Multireference configuration interaction|MCSCF]] and [[MRCI]], which are very expensive and delicate methods.  This is further complicated by the fact that definition of vibronic couplings requires electronic [[wavefunctions]]. Unfortunately, wavefunction based methods are usually too expensive for larger systems and popular methods for larger systems such as [[density functional theory]] and [[molecular mechanics]] cannot generate wave function information.
As a result, direct evaluation of vibronic couplings are mostly limited to very small molecules.  The magnitude of vibronic coupling is often introduced as an [[Empirical method|empirical]] parameter determined by reproducing experimental data.
 
Alternatively, one can avoid explicit use of derivative couplings by switch from the [[adiabatic process (quantum mechanics)|adiabatic]] to the [[diabatic]] representation of the [[potential energy surface]]s.  Although rigorous validation of a diabatic representation requires knowledge of vibronic coupling, it is often possible to construct such diabatic representations by referencing the continuity of physical quantities such as dipole moment, charge distribution or orbital occupations.  However, such construction requires detailed knowledge of a molecular system and introduces significant arbitrariness. Diabatic representations constructed with different method can yield different results and the reliability of the result relies on the discretion of the researcher.
 
==Theoretical development==
Perhaps the earliest examples of the importance of vibronic coupling were found during the 1930s. In 1934 [[Renner&ndash;Teller effect|Renner]] wrote about the vibronic coupling in an electronically excited Π-state in CO<sub>2</sub>. Calculations of the lower [[excited state|excited levels]] of [[benzene]] by Sklar in 1937 (with the valence bond method) and later in 1938 by [[Maria Goeppert-Mayer|Goeppert-Mayer]] and Sklar (with the [[molecular orbital]] method) demonstrated a correspondence between the theoretical predictions and experimental results of the benzene [[spectroscopy|spectrum]]. The benzene spectrum was the first qualitative computation of the efficiencies of various vibrations at inducing intensity absorption.<ref>{{cite book |last=Fischer |first=Gad |title=Vibronic Coupling: The Interaction between the Electronic and Nuclear Motions |publisher=Academic Press |location=New York |year=1984 |isbn=0-12-257240-8 }}</ref>
 
== See also ==
*[[Born&ndash;Huang approximation]]
*[[Born-Oppenheimer approximation]]
*[[Conical intersection]]
 
==References==
{{reflist}}
 
[[Category:Quantum chemistry]]
[[Category:Molecular vibration]]
[[Category:Dynamics]]

Latest revision as of 07:02, 25 July 2014

It's a good idea to have your own representative with you while going to purchase a newly constructed condominium. You may not be aware of this, but while you approach the sales office regarding a new condominium development; the gross sales workers is there to represent the interests of the builder.

Looking at all these points, they aid you select and choose one of the best. A sensible choice would be to search for property near the MRT (Mass Rapid Transit) as it will make it simpler for you to get round with the railway station connecting the complete city to state. The country is clean, the food is great. Real estate brokers love this place and may present you the very best it has to supply. It could even be clever to take a look at London property costs, as they don't seem to be only inexpensive but additionally might enhance and would profit you as an investment purpose.

Moreover, we're doable coming right into a period of weakening rental demand. Over the last few years, within the backdrop of a powerful financial system and rising worldwide workforce, rental demand averaged around forty two,000 items. Going ahead, offered that Singapore is taking a look at a slowing charge of GDP and international workforce improvement, the growth in rental demand is extra likely new launch fernvale to be decrease than the expansion of rental present (from the huge improve in completed items), leading to lower rental yields and high vacancy fees. There is singapore property prices no harm in double-checking our information regarding the HDB market - especially since policies are frequently being reviewed and adjusted.

Whereas Napic doesn't have a housing affordability index, a tricky calculation reveals that the standard worth of RM273,00 is about 5.6 occasions that of a median annual family earnings of RM48,000. The widespread price of a KL home is now a steep 13 occasions that of the widespread metropolis family income of RM54,000 and a doable signal that the market is headed for a bubble. The sharp enhance in costs is alleged to be on the very least partly attributable to speculative demand as patrons snap up a variety of properties within the hope that costs will carry on spiralling upward '" despite low occupancy rates that may affect rental yields. Concerning the Writer

Recording the underside variety of new models being launched in August with just one,118 items out there, the August URA figures additionally showed an anticipated dip with a total of 1,539 fashions bought. Consistent with PropNex, this was the lowest variety of new private residential transactions (together with Government Condominium) ecotech @ sunview in 2012, at a drop of 25.5 percent m-on-m, with sixty two percent of the general fashions offered inside the Exterior Central Region. If initiatives akin to Eco and Riversails are able to hit the launch pad in September, new personal home gross sales is more more likely to rebound throughout the private property market."

As we speak, the Asian property market (particularly in Singapore, Hong Kong and China) is being supported by ‘phoney' cash. Money is printed endlessly in the trillions of dollars by irresponsible governments for political motives. Banks are both reducing their reserve rates or chopping interest rates and these have fuelled the influx of extra hot cash. The money is finding its method into Asian markets like Singapore, within the hopes of so-referred to as higher returns and inflating many asset bubbles.

Another excuse why increasingly property owners are acquiring property administration providers Warranwood is that they make sure that the gathering of lease and regular reporting that keeps them abreast of the scenario concerning their real property. On the Lakeville New launch you'll be able to discover a new way of life where the whole lot you have ever dreamt of is feasible. You get consolation, comfort and privacy multi functional place. As soon as you live in Lakeville, you'll by no means wish to leave! Alan Cheong, Research Head at Savills Singapore, said that whereas Jurong is an established town, newer estates reminiscent of Sengkang, Pasir Ris and Punggol have overshadowed it in terms of new executive and personal condominium launches. Energetic secondary market for simple exit of property investments.

Many traders have shunned away from shopping for residential properties in Singapore due to the steep stamp duties in place. Relying on the quantum you purchase your property , you can positively anticipate to pay at the very least five to six figures simply in property taxes alone. Nevertheless, there are nonetheless no property taxes in place with regards to industrial properties Therefore, it's a sexy purchase as the money might be put to raised use or translate to better rental yield.