Enthalpic nature of the CH/π interaction involved in the recognition of carbohydrates by aromatic compounds, confirmed by a novel interplay of NMR, calorimetry, and theoretical calculations

Journal of the American Chemical Society

Volumn 131, Issue 50, 2009, Pages 18129-18138

  Ramírez Gualito, Karla ^a   Alonso Ríos, Rosa ^a   Quiroz García, Beatriz ^a   Rojas Aguilar, Aarón ^b   Díaz, Dolores ^c   Jiménez Barbero, Jesús ^c   Cuevas, Gabriel ^a  

^a UNIVERSIDAD NACIONAL AUTÓNOMA DE MÉXICO   (Mexico)

^b DEPARTAMENTO DE FÍSICA   (Mexico)

^c CENTRO DE INVESTIGACIONES BIOLÓGICAS   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ANOMERIC POSITION; BENZENE MOLECULES; CALVET MICROCALORIMETRY; DIFFERENT EFFECTS; ENTHALPY OF SOLVATION; GALACTOPYRANOSE; GALACTOPYRANOSIDE; INTERACTION ENERGIES; METHOXY; METHOXY GROUP; METHYL GROUP; MOLECULAR REGION; NMR DATA; NON-POLAR; PYRANOSE; SPECIFIC INTERACTION; STABILIZATION ENERGY; STACKING INTERACTION; THEORETICAL CALCULATIONS;

CARBOHYDRATES; ENTHALPY; FLUORINE CONTAINING POLYMERS; HYDROCARBONS; MOLECULAR BIOLOGY; MOLECULAR RECOGNITION; MOLECULES; NUCLEAR MAGNETIC RESONANCE;

BENZENE;

1,2,3,4,6 PENTA O ACETYL BETA DEXTRO GALACTOPYRANOSE; ACETIC ACID DERIVATIVE; AROMATIC COMPOUND; BENZENE; CARBOHYDRATE DERIVATIVE; METHYL 2,3,4,6 TETRA O METHYL ALPHA DEXTRO GALACTOPYRANOSIDE; METHYL 2,3,4,6 TETRA O METHYL ALPHA DEXTRO MANNOPYRANOSIDE; METHYL 2,3,4,6 TETRA O METHYL BETA DEXTRO GALACTOPYRANOSIDE; METHYL GROUP; PROTON; PYRANOSIDE; UNCLASSIFIED DRUG;

ARTICLE; CALCULATION; CONTROLLED STUDY; ENERGY; ENTHALPY; EPIMER; GEOMETRY; MICROCALORIMETRY; MOLECULAR INTERACTION; MOLECULAR RECOGNITION; MOLECULE; NUCLEAR MAGNETIC RESONANCE; SOLVATION; SUBSTITUTION REACTION;

BENZENE; CALORIMETRY, DIFFERENTIAL SCANNING; CARBOHYDRATE CONFORMATION; CARBOHYDRATES; HYDROCARBONS, AROMATIC; HYDROGEN BONDING; MAGNETIC RESONANCE SPECTROSCOPY; METHYLATION; MODELS, MOLECULAR; MODELS, THEORETICAL; THERMODYNAMICS;

EID: 72449187087     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja903950t     Document Type: Article

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