Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/357599
Type: Artigo
Title: Stereoelectronic effects of the glycosidic linkage on the conformational preference of d-sucrose
Author: Rozada, Thiago de Castro
Pontes, Rodrigo Meneghetti
Rittner, Roberto
Basso, Ernani Abicht
Abstract: The stereoelectronic effects involved in the conformations shown by D-sucrose were analysed at the M06-2X/6-31++G(d,p) level, both under vacuum and in water with the continuum solvation model IEF-PCM, and employing the natural bond orbital theory (NBO) and non-covalent interactions (NCI). Different groups of conformations for D-sucrose in relation to the glycosidic linkage were evaluated and the results showed that not only were hydrogen bonds important to explain the relative energy observed, but it was also necessary to consider any stabilizing orbital interactions involving the glycosidic linkage. The most stable conformation observed in water had dihedral angles for the glycosidic linkage with values of 110.8° and −44.9° for ϕ and ψ, respectively.
Subject: Sacarose
Country: Estados Unidos
Editor: Royal Society of Chemistry
Rights: Fechado
Identifier DOI: 10.1039/c6ra24413k
Address: https://pubs.rsc.org/en/content/articlelanding/2016/ra/c6ra24413k#!divAbstract
Date Issue: 2016
Appears in Collections:IQ - Artigos e Outros Documentos

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.