HF/6-31G* Energy Surfaces for Disaccharide Analogs

Alfred D. French*, Anne Marie Kelterer, Glenn P. Johnson, Michael K. Dowd, Christopher J. Cramer

*Korrespondierende/r Autor/in für diese Arbeit

Publikation: Beitrag in einer FachzeitschriftArtikel

Abstract

The HF/6-31G* level of theory was used to calculate relaxed potential energy surfaces for 12 analogs of disaccharides. The analogs were made by replacing glucose with tetrahydropyran and fructose with 2-methyltetrahydrofuran. Molecules had zero, one or two anomeric carbon atoms, and di-axial, axial-equatorial, and di-equatorial linkages. Despite the absence of hydroxyl groups, the surfaces account well for conformations that are observed in crystals of the parent disaccharides. Thus, torsional energy and the simple bulk of ring structures are major factors in determining disaccharide conformation. The contour shapes around the global minima depend on the number of anomeric carbons involved in the linkage, while the presence of alternative minima that have relative energies less than 4 kcal/mol mostly requires equatorial bonds. However, molecules with two adjacent anomeric centers gave exceptions to these rules. Flexibility values related to a partition function show that the di-axial trehalose analog is the most rigid. The di-equatorial pseudodisaccharide analog with no anomeric centers is most flexible. Reproduction of these surfaces is proposed as a simple test of force fields for modeling carbohydrates. Also, these surfaces can be used in a simple hybrid method for calculating disaccharide energy surfaces.

Originalspracheenglisch
Seiten (von - bis)65-78
Seitenumfang14
FachzeitschriftJournal of Computational Chemistry
Jahrgang22
Ausgabenummer1
DOIs
PublikationsstatusVeröffentlicht - 15 Jan 2001

ASJC Scopus subject areas

  • !!Chemistry(all)
  • !!Safety, Risk, Reliability and Quality

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