English   español  
Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/66132
Share/Impact:
Statistics
logo share SHARE logo core CORE   Add this article to your Mendeley library MendeleyBASE

Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL
Exportar a otros formatos:

Title

Simultaneous interaction of tetrafluoroethene with anions and hydrogen-bond donors: A cooperativity study

AuthorsAlkorta, Ibon ; Blanco, F.; Elguero, José
Issue Date2009
PublisherAmerican Chemical Society
CitationJournal of Chemical Theory and Computation 5: 1186- 1194 (2009)
AbstractA computational study of the complexes formed by tetrafluoroethylene, C2F4, with anions has been carried out by means of density functional theory (DFT) and second-order Mö ller-Plesset (MP2) computational methods, up to MP2/aug-cc-pVTZ level. In addition, the possibility of cooperativity in the interaction of anions and hydrogen-bond donors (FH, ClH, and H2O) when interacting with different faces of the C 2F4 molecule has been explored. Electron density of the complexes has been analyzed by means of atoms in molecules (AIM) methodology, while natural bond orbital (NBO) methodology has been used to characterize the orbital interaction. In addition, natural energy decomposition analysis (NEDA) has been applied to analyze the source of the interaction. The energetic results indicate that C2F4 is a weaker anion receptor than C 6F6, but in combination with the anions, it became a stronger hydrogen acceptor than C2H4. Cooperativity effects are observed in YH·C2F4 ·X - clusters. In C2F4 ·X- complexes the dominant attractive terms are the electrostatic and polarization ones, while in YH·C2F4 ·X- complexes the charge transfer increases significantly, becoming the most important term for most of the FH and ClH complexes studied here. © 2009 American Chemical Society.
Publisher version (URL)http://dx.doi.org/10.1021/ct800444e
URIhttp://hdl.handle.net/10261/66132
DOI10.1021/ct800444e
Identifiersdoi: 10.1021/ct800444e
issn: 1549-9618
e-issn: 1549-9626
Appears in Collections:(IQM) Artículos
Files in This Item:
File Description SizeFormat 
accesoRestringido.pdf15,38 kBAdobe PDFThumbnail
View/Open
Show full item record
Review this work
 


WARNING: Items in Digital.CSIC are protected by copyright, with all rights reserved, unless otherwise indicated.