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Computational modeling of inclusion complexes of β‐cyclodextrin with enantiomers of salsolinol, N ‐methyl‐salsolinol, and 1‐benzyl‐tetrahydroisoquinoline
Author(s) -
Huang MingJu,
Quan Zhe,
Liu YiMing
Publication year - 2008
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.21852
Subject(s) - chemistry , oniom , enantiomer , capillary electrophoresis , tetrahydroisoquinoline , cyclodextrin , stereochemistry , structural isomer , molecule , computational chemistry , molecular model , organic chemistry , chromatography
Capillary electrophoresis with β‐CD as a chiral selector has successfully separated the two enantiomers of salsolinol, N ‐methyl‐salsolinol, and 1‐benzyl‐tetrahydroisoquinoline (BTIQ). The migration times of each enantiomer in capillary electrophoresis reflect the stability of their β‐CD inclusion complexes. This paper reports a computational modeling study of the inclusion complexes of β‐cyclodextrin (β‐CD) with salsolinol, N ‐methyl‐salsolinol, and BTIQ by using PM3 (Parametric Method 3) semiempirical molecular orbital calculations and the ONIOM hybrid method. Two types of the inclusion complexes, cis‐ and trans‐orientations, are considered for each enantiomer of the guest molecules, salsolinol, N ‐methyl‐salsolinol, and BTIQ. In the cis‐orientation, the nitrogen in the salsolinol, N ‐methyl‐salsolinol, and BTIQ points toward the secondary hydroxyls of the β‐CD, while in the trans‐orientation, the nitrogen in salsolinol, N ‐methyl‐salsolinol, and BTIQ points toward the primary hydroxyls of the β‐CD. We found that the stabilization energies of these inclusion complexes from these PM3 and ONIOM different methods correlate very well with the migration order deduced from the study of capillary electrophoretic separation. © 2008 Wiley Periodicals, Inc. Int J Quantum Chem, 2009