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Issue title: Computational aspects of electric polarizability calculations: Atoms, Molecules and clusters, Part I
Article type: Research Article
Authors: Diedrich, C. | Causemann, S. | Grimme, S.; *
Affiliations: Theoretische Organische Chemie, Organisch-Chemisches Institut der Universität Münster, Corrensstraße 40, D-48149 Münster, Germany
Correspondence: [*] Corresponding author. E-mail: grimmes@uni-muenster.de.
Abstract: The optical rotations (OR) of five chiral organic molecules have been calculated by time-dependent density functional response theory (TDDFT) employing four different density functionals. The results are compared with experimental gas phase data in order to explore the inherent accuracy of the functionals. The theoretical results obtained with the BHLYP hybrid functional including 50% “exact” Hartree-Fock exchange compare very well with the experimental data and also better with those derived from the gas-phase than from solution. Non-hybrid functionals show a tendency to overestimate the OR. The anomalous behavior of the methyloxirane molecule which shows sign changes with solvent and excitation frequency is discussed.
Keywords: time dependent density functional theory, optical rotation, organic molecules
DOI: 10.3233/JCM-2004-4306
Journal: Journal of Computational Methods in Sciences and Engineering, vol. 4, no. 3, pp. 293-300, 2004
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