期刊
JOURNAL OF PHYSICAL CHEMISTRY A
卷 115, 期 51, 页码 14677-14686出版社
AMER CHEMICAL SOC
DOI: 10.1021/jp2093725
关键词
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资金
- Center for Computational Research at the University at Buffalo
- University at Buffalo Chemistry Department
- National Science Foundation [CHE-0952253]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [0952253] Funding Source: National Science Foundation
A number of density functionals, including 'pure' (nonhybrid) functionals, global hybrids, and range-separated hybrids, were used to calculate the electronic circular dichroism (CD) spectra of 10 tris-bidentate transition metal complexes. The results are compared to one another and to experimental CD spectra, in an effort to illustrate the shortcomings of particular approximations in time-dependent density functional theory (TDDFT). The use of an origin invariant formalism to calculate magnetic transition dipole moments with the help of gauge-including atomic orbitals (GIAOs) is also investigated. With valence basis sets of moderate flexibility, good agreement between GIAO results and rotatory strengths calculated from the dipole-velocity representation is obtained for selected test cases. Empirically broadened vertical CD spectra calculated with the global hybrid functionals B3LYP and PBE0 are found to agree overall the best with experimental CD spectra.
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