Issue 6, 2001

Molecular structure and gas-phase reactivity of clonidine and rilmenidine: Two-layered ONIOM calculations

Abstract

The geometries of various tautomers and rotamers of clonidine and rilmenidine in both anionic and protonated forms, were optimized using the two-layered ONIOM(B3LYP 6-311 + G(d,p): MNDO) method. The calculations showed that, in agreement with experiment, clonidine exists as the more stable imino tautomer. The tautomer containing the amino group is less stable by about 30 kJ mol−1. Rilmenidine also exists in two forms (amino and imino), the amino tautomer being more stable by 5 kJ mol−1. The computed stable conformation for the clonidine species is characterized by the phenyl and imidazolidine rings being perpendicular to each other. In the case of the rilmenidine tautomers and ionised forms, the oxazoline and dicyclopropyl moieties are in a mutual gauche conformation. In contrast to the parent neutral molecule of clonidine, ionization caused considerable geometric changes in the clonidine anions. The oxazoline derivative of rilmenidine is by about 50–60 kJ mol−1, a weaker acid than the imidazoline derivative clonidine. The primary protonation sites are the imidazolidine and oxazoline parts of the drugs. Rilmenidine is slightly less basic than clonidine. The proton affinities of clonidine and rilmenidine were computed to be − 999 and − 996 kJ mol−1, respectively. The clonidine base was found to be substantially more lipophilic than the base of rilmenidine.

Supplementary files

Article information

Article type
Paper
Submitted
01 Dec 2000
Accepted
19 Jan 2001
First published
27 Feb 2001

Phys. Chem. Chem. Phys., 2001,3, 901-907

Molecular structure and gas-phase reactivity of clonidine and rilmenidine: Two-layered ONIOM calculations

M. Remko, O. A. Walsh and W. Graham Richards, Phys. Chem. Chem. Phys., 2001, 3, 901 DOI: 10.1039/B009660L

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