Geometric structures and electronic properties of HIV-1 proteinase inhibitor : C60 derivatives

Abstract

Quantum chemical methods were performed to study structure and electronic properties of a series of C60 derivatives. The integrated, ONIOM moleculaar orbital method was applied to optimize the structure of all compounds while the DFT/B3LYP (6-31G (d)) calculations were performed to examine molecular and electronic properties. It was found that strongest effect of functional group on the net charges takes place on the linked atoms between C60 and its side chain. The functional group leads to the changes of atomic net charges on the C60 surface up to 5 A far from C-C bond where the functional group binds to the surface. Two localized electrostatic potential regions are observed, for the selected compounds, near the hydroxyl oxygen and the hydroxyl hydrogen. The hydroxyl hydrogen atom is the center for most positive potential. These electrostatic features are likely to be the modulator of hydrophobicity or lipophilicity of the compounds and, hence, indicate how they interact with the receptor.