dc.creatorFuentealba Rosas, Patricio
dc.creatorSantos, Juan C.
dc.date.accessioned2018-12-20T14:06:15Z
dc.date.available2018-12-20T14:06:15Z
dc.date.created2018-12-20T14:06:15Z
dc.date.issued2011
dc.identifierCurrent Organic Chemistry, Volumen 15, Issue 20, 2018, Pages 3619-3626
dc.identifier13852728
dc.identifier10.2174/138527211797636200
dc.identifierhttps://repositorio.uchile.cl/handle/2250/153874
dc.description.abstractThe Electron Localization Function (ELF) has played in the last time an important role in understanding the special characteristics of the chemical bond. The chemical interpretation of the ELF as an indicator of the regions of the space where it is most probable to find a localized electron pair has been of great value in order to understand some complex chemical bonds. In this work, the ELF has been used to study the delocalization and aromatic character of a diversity of molecules. It is shown that whereas the analysis of the total ELF does not provide clear information about aromaticity, the separation of the function on its σ and π parts yields indeed valuable information about it. Moreover, it is possible to construct a quantitative scale of aromaticity. It is also shown that the use of the ELF to understand aromaticity is complementary to other methodologies. The study includes mono substituted benzene derivatives, cyclic organic compounds, borazine molecule and the mechanism of
dc.languageen
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceCurrent Organic Chemistry
dc.subjectAromaticity
dc.subjectElectron localization
dc.subjectELF
dc.titleElectron localization function as a measure of electron delocalization and aromaticity
dc.typeArtículo de revista


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