期刊
JOURNAL OF CHEMICAL THEORY AND COMPUTATION
卷 12, 期 2, 页码 535-548出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jctc.5b00721
关键词
-
资金
- NOTUR project at the Norwegian Research Council [2920k]
We have calculated the electronic optical rotation of seven molecules using coupled cluster singles-doubles (CCSD) and the second-order approximation (CC2) employing the aug-cc-pVXZ (X = D, T, or Q) basis sets. We have also compared to time dependent density functional theory (TDDFT) by utilizing two functionals B3LYP and CAM-B3LYP and the same basis sets. Using relative and absolute error schemes, our calculations demonstrate that the CAM-B3LYP functional predicts optical rotation with the minimum deviations compared to CCSD at lambda = 355 and 589.3 nm. Furthermore, our results illustrate that the aug-cc-pVDZ basis set provides the optical rotation in good agreement with the larger basis sets for molecules not possessing small-angle optical rotation at lambda = 589.3 nm. We have also performed several two-point inverse power extrapolations for the basis set convergence, i.e., OR infinity, + AX(-n), using the CC2 model at lambda = 355 and 589.3 nm. Our results reveal that a two-point inverse power extrapolation with the aug-cc-pVTZ and aug-cc-pVQZ basis sets at n = 5 provides optical rotation deviations similar to those of aug-cc-pVSZ with respect to the basis limit.
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