Fernando Obledo-Benicio, Nancy E Magaña-Vergara, K. Pineda‐Urbina
Jun 1, 2020
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Journal
Journal of Molecular Structure
Abstract
Abstract Four compounds derived from 2-hydroxy and 2-mercaptobenzimidazole were synthesized and characterized by FT-IR spectroscopy, nuclear magnetic resonance and elemental analysis. Two of the resulting compounds –diethyl 2-oxo-1H benzo[d]imidazole-1,3(2H)-dicarboxylate and diethyl 2-thioxo-1H benzo[d]imidazole-1,3(2H)-dicarboxylate– were crystallized and analyzed by X-ray diffraction. The former presented intermolecular interactions of bidentate hydrogen-bonds and the formation of R 2 2 (10) rings via C–H⋯O C, resulting in a stacking arrangement while the latter had a zig-zag arrangement due to the intermolecular aromatic interaction C–H⋯O C. A computational conformational study was made to support and explain the resulting structures stabilities. Furthermore, a QTAIM analysis was performed to study the nature of the intramolecular 1,5-type O⋯O and S⋯O interactions.