Abstract
We report the implementation of a method for the calculation of optical rotation. This method is based on the time-dependent density-functional theory and utilizes time-periodic magnetic-field-dependent basis functions. The calculations are based on a density fit. It is demonstrated that additional terms in the analytical expression appearing from derivatives of the approximated Coulomb potential are necessary to provide the gauge-origin independence of the results within a given numerical accuracy. Contributions from these terms also restore the symmetry between the electric and magnetic perturbations in the optical rotation tensor.
| Original language | English |
|---|---|
| Article number | 114103 |
| Journal | Journal of Chemical Physics |
| Volume | 123 |
| Issue number | 11 |
| DOIs | |
| State | Published - Sep 15 2005 |
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