Evaluates solvation models and conformational analyses in organic molecules, suggesting optimal methods.
To provide a guide for selecting appropriate calculation methods for conformational analyses of organic molecules with explicit consideration of solvation effects, the A-values of twenty-two substituents were computed with solvation corrections across multiple solvation models. In addition, conformational equilibrium analyses of 1,4- and 1,2-trans-difluorocyclohexanes were performed as complementary benchmark systems, and a comprehensive evaluation was achieved through integration of both datasets. Comparison with reported experimental data furnished a robust benchmark for identifying the optimal combination of solvation models and theoretical levels for energy calculation and geometry optimization.
No takes yet. Share an insight, caveat, or question.
Yamada et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: