Please use this identifier to cite or link to this item: http://repositorio.ufla.br/jspui/handle/1/32802
metadata.artigo.dc.title: A halogen bond does not dictate the conformational preferences of cis-1,3-disubstituted cyclohexanes
metadata.artigo.dc.creator: Silla, Josué M.
Freitas, Matheus P.
metadata.artigo.dc.subject: Halogen bonds
Intermolecularly interacting species
Conformational stability
Ligações de halogéneo
Espécies interagindo intermolecularmente
Estabilidade conformacional
metadata.artigo.dc.publisher: Royal Society of Chemistry
metadata.artigo.dc.date.issued: 2016
metadata.artigo.dc.identifier.citation: SILLA, J. M.; FREITAS, M. P. A halogen bond does not dictate the conformational preferences of cis-1,3-disubstituted cyclohexanes. Cambridge, v. 14, p. 8610-8614, 2016.
metadata.artigo.dc.description.abstract: Halogen bonds are defined as interactions between halogens and a Lewis base in which the halogen (X) acts as the electrophilic species, and is typically explained by the presence of a σ-hole at the end of the C–X bond. Despite the important role of the halogen bond in intermolecularly interacting species, e.g. in acid–base reactions, enzyme inhibition and the supramolecular architecture, this interaction was not found to control the conformational equilibrium of some small model molecules, namely cis-1,3-disubstituted cyclohexanes. In addition, the attraction between the electrophilic (σ-hole) and nucleophilic regions is used to explain that the halogen bond was weaker than that in the species with parallel C–X bonds. Therefore, intramolecular halogen bonds should be used with caution to explain the conformational stability of organic compounds.
metadata.artigo.dc.identifier.uri: https://pubs.rsc.org/en/Content/ArticleLanding/2016/OB/c6ob01635a#!divAbstract
http://repositorio.ufla.br/jspui/handle/1/32802
metadata.artigo.dc.language: en_US
Appears in Collections:DQI - Artigos publicados em periódicos

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