dc.creatorDias, Luiz C
dc.creatorFerreira, Marco A B
dc.creatorTormena, Claudio F
dc.date2008-Jan
dc.date2015-11-27T13:13:33Z
dc.date2015-11-27T13:13:33Z
dc.date.accessioned2018-03-29T01:08:09Z
dc.date.available2018-03-29T01:08:09Z
dc.identifierThe Journal Of Physical Chemistry. A. v. 112, n. 2, p. 232-7, 2008-Jan.
dc.identifier1089-5639
dc.identifier10.1021/jp709601w
dc.identifierhttp://www.ncbi.nlm.nih.gov/pubmed/18154324
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/198142
dc.identifier18154324
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1298375
dc.descriptionWe have investigated the electronic impact of the R protecting group (TBS or PMB) in the conformational equilibrium of alpha-methyl substituted alcohols 1 (R = TBS) and 2 (R = PMB). The conformational analysis and (1)H NMR experiments for alcohols 1 and 2 reflect the tendency for the existence of hydrogen-bonded conformations. The intrinsic low basicity of silyl ethers does not affect the capacity of the oxygen attached to the silicon atom in forming intramolecular hydrogen bonds. We showed that the extents of the hydrogen bonds in silyl and alkyl ethers are determined by several properties, such as orbital interactions, lone pair hybridizations, and lone pair energies, and not just by the electronic occupancy of the donor atom. The populational analysis of NBO allowed understanding the intra- and intermolecular hydrogen bonds between the OH group and oxygen bonded to silicon as well as to alkyl ethers, concluding that there are distinct lone pair contributions.
dc.description112
dc.description232-7
dc.languageeng
dc.relationThe Journal Of Physical Chemistry. A
dc.relationJ Phys Chem A
dc.rightsfechado
dc.rights
dc.sourcePubMed
dc.titleIntra- And Intermolecular Hydrogen Bonds In Alkyl And Silyl Ethers: Experimental And Theoretical Analysis.
dc.typeArtículos de revistas


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