Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/74865
Título: Conformational study of the open-chain and furanose structures of d-erythrose and d-threose
Autores/as: Azofra Mesa, Luis Miguel 
Alkorta, Ibon
Elguero, José
Popelier, Paul L.A.
Clasificación UNESCO: 2307 Química física
Fecha de publicación: 2012
Publicación seriada: Carbohydrate research (Print) 
Resumen: The potential energy surfaces for the different configurations of the D-erythrose and D-threose (open-chain, α- and β-furanoses) have been studied in order to find the most stable structures in the gas phase. For that purpose, a large number of initial structures were explored at B3LYP/6-31G(d) level. All the minima obtained at this level were compared and duplicates removed. A further reoptimization of the remaining structures was carried out at B3LYP/6-311++G(d,p) level. We characterized 174 and 170 minima for the open-chain structures of D-erythrose and D-threose, respectively, with relative energies that range over an interval of just over 50kJ/mol. In the case of the furanose configurations, the number of minima is smaller by approximately one to two dozen. G3B3 calculations on the most stable minima indicate that the α-furanose configuration is the most stable for both D-erythrose and D-threose. The intramolecular interactions of the minima have been analyzed with the Atoms in Molecules (AIM) and Natural Bond Orbital (NBO) methodologies. Hydrogen bonds were classified as 1-2, 1-3 or 1-4, based on the number of C-C bonds (1, 2 and 3, respectively) that separate the two moieties participating in the hydrogen bond. In general, the AIM and NBO methodologies agree in the designation of the moieties involved in hydrogen bond interactions, except in a few cases associated to 1-2 contact which have small OH···O angles.
URI: http://hdl.handle.net/10553/74865
ISSN: 0008-6215
DOI: 10.1016/j.carres.2012.06.011
Fuente: Carbohydrate research [ISSN 0008-6215], v. 358, p. 96-105
Colección:Artículos
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