Différences entre les versions de « ELF abstracts page »
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<font color=red> '''SPEAKERS :''' please add below, in your own section, your title talk and abstract : </font> | <font color=red> '''SPEAKERS :''' please add below, in your own section, your title talk and abstract : </font> | ||
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* click on your name in the ''' "Contents" ''' box below, this will lead you to your own section; | * click on your name in the ''' "Contents" ''' box below, this will lead you to your own section; | ||
* your section starts with your name as the title line, click on '''[<font color=blue>edit</font>]''' (far right). | * your section starts with your name as the title line, click on '''[<font color=blue>edit</font>]''' (far right). | ||
Version du 20 mai 2010 à 17:43
SPEAKERS : please add below, in your own section, your title talk and abstract :
- first : log in;
- click on your name in the "Contents" box below, this will lead you to your own section;
- your section starts with your name as the title line, click on [edit] (far right).
The order of abstract follow the program of the workshop.
E. Alikhani
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P. Hiberty
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C. Lepetit
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M-M. Rohmer
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B. De Courcy
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H. Jamet
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G. A. Cisneros
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X. Assfeld
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H. S. Rzepa
Department of Chemistry, Imperial College London
ELF and the Nature of Triple bonds
A recent report of the species HOS≡CH by Schreiner, Mloston and co-workers1 speculated upon the nature of the SC bond; did it have triple significant bond character? Of the various techniques these authors used for the analysis, neither QTAIM nor ELF was employed. I initially filled this gap by a post on my blog2, and followed this by a full article submitted for publication more conventionally3. The results of this investigation will be presented at the workshop, including a rather surprising conclusion regarding the nature of triple bonds themselves in relation to the degree of charge-shift character they display4. The hypothesis so generated was then extended to investigating the nature of metal-metal multiple bonds, particularly Cr-Cr whose compounds are purported to exhibit homonuclear quadruple or quintuple bonds5. These systems also appear to sustain remarkably high charge-shift character and most intriguing ELF behaviour. The issue for discussion in the workshop is therefore whether or not ELF (combined with QTAIM) is indeed revealing something new about the nature of the triple and higher order homonuclear (metal) bond.
The talk will appear @www.ch.ic.ac.uk/rzepa/talks/elf10 and will feature rotatable ELF isosurfaces and models.
References
[1] P. R. Schreiner, H. P. Reisenauer, J. Romanski, and G. Mloston, Angew. Chemie. 2009, 48, 8133-8136. DOI: 10.1002/anie.200903969
[2] H. S. Rzepa, Blog and follow up
[3] H. S. Rzepa, submitted for publication, 2010.
[4] S. Shaik, D. Danovich, W. Wu and P. C. Hiberty, Nature Chem., 2009, 1, 443-449. DOI: 10.1038/nchem.327
[5] For initial speculations, see blog.
M. Yanez
Departamento de Química, C-9. Universidad Autónoma de Madrid. Cantoblanco, 28049-Madrid. Spain
ELF as a useful tool to understand chemical bonding in challenging cases
Quite unexpectedly, substituent effects on the structure of iminoboranes are opposite to those observed for the acetylene derivatives in spite of the fact that both series of compounds are isoelectronic. [1] More importantly these dissimilarities cannot be easily explained in terms of the atoms in molecules (AIM) theory or in terms of the population of the πBN* or πCC* antibonding orbitals. In some molecules a decrease (increase) of the electron density is unexpectedly reflected in a shortening (lengthening) of the bond. Conversely, the ELF analysis offers a clear picture of the substituent effects on the CC and BN bonding. The dissimilarities between acetylene- and iminoborane derivatives are primarily a consequence of the strong electronegativity difference between the B and N atoms in the iminoboranes. This difference is the origin of the significant distortion of the BN bonding electron density in iminoboranes, which is not seen in the corresponding acetylene analogues.
References
[1] O. Mó; M. Yáñez; A. Martín Pendás; J.E. Del Bene; I. Alkorta and J. Elguero, Phys. Chem. Chem. Phys. 9, 3970 (2007)
P. J. MacDougall
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J. Angyan
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M. Causa
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J. Contreras-Garcia
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D. L. Cooper
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A. Lüchow
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E. P. Fowe
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S. Grabowski
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A. M. Pendas
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E. Matito
Institute of Physics, University of Szczecin, Poland
The Electron Localization Function at the Correlated Level: A Natural Orbital Formulation.
The calculation of the electron localization function (ELF) at the correlated level carries the computational expense of the second-order density matrix (DM2).1 In this work we put forward an approximation for the calculation of the ELF at the correlated level without using the DM2.2 In particular, we use approximate expressions for the DM2 based on the formula for the monodeterminantal wavefunctions (X-HF in the graph below) and the formula of Müller in terms of natural orbitals.3 The approximation has been tested in a set of molecules, NH3, CO2, H2O, CO, CN-, NO+, N2, H2O2, F2 and FCl-, which have been calculated using a plethora of methods: HF, B3LYP, MP2, CISD, CCSD and CASSCF. For these methods/molecules we calculate the atomic population and its variance for each ELF basin.
References
[1] Matito E., Silvi B., Duran M. and Solà M., J. Chem. Phys. 125, 024301 (2006)
[2] Feixas F., Matito E., Duran M., Solà M. and Silvi B., in preparation.
[3] Müller A.M.K., Phys. Lett. 105A, 446 (1984)
D. Borgis
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R. Vuillemier
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J. Cioslowski
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J. Pilmé
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R. Nesper
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Y. Grin
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J-F. Halet
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U. Wedig
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R. Weihrich
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P. Raybaud
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E. Dumont
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N. Chéron
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S. Berski
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L. Joubert
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H. Bolvin
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A. Delalande
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R. Nalewajski
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A. Scemama
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J. Tao
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I. Fourré
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H. Gérard
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N. Russo
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