Optimal configurations of "capped" β-cyclodextrin dimers in water maximise hydrophobic association

ChemPhysChem

Volumn 11, Issue 2, 2010, Pages 452-459

  Riedaa Gamieldien, M ^b   Maestre, Itziar ^a   Jaime, Carlos ^a   Naidoo, Kevin J ^b  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

^b UNIVERSITY OF CAPE TOWN   (South Africa)

Author keywords

Cyclodextrins; Dimerization; Hydrophobic effect; Molecular dynamics; Supramolecular chemistry

Indexed keywords

CYCLODEXTRINS; DICHROISM; DIMERIZATION; FREE ENERGY; HYDROGEN BONDS; HYDROPHOBICITY; MOLECULAR DYNAMICS; NAPHTHALENE; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SUPRAMOLECULAR CHEMISTRY;

BETA-CYCLODEXTRIN; DIMER CONFIGURATION; FREE-ENERGY CALCULATIONS; HEAD-TO-HEAD CONFIGURATIONS; HYDROPHOBIC ASSOCIATION; HYDROPHOBIC EFFECT; NAPHTHYL GROUPS; TAIL ARRANGEMENT;

DIMERS;

EID: 75249089431     PISSN: 14394235     EISSN: 14397641     Source Type: Journal    
DOI: 10.1002/cphc.200900541     Document Type: Article

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