Abstract
The chirality of molecules expresses itself, for example, in the fact that a solution of a chiral molecule rotates the plane of linear polarised light. The underlying molecular property is the optical rotatory power (ORP) tensor, which according to time-dependent perturbation theory can be calculated as mixed linear response functions of the electric and magnetic dipole moment operators. Applying a canonical transformation of the Hamiltonian, which reformulates the magnetic dipole moment operator in terms of the operator for the torque acting on the electrons, the ORP of a molecule can be partitioned into atomic and group contributions. In the present work, we investigate the transferability of such individual contributions in a series of small, chiral molecules: hydrogen peroxide, methyl hydroperoxide and dimethyl peroxide. The isotropic atomic or group contributions have been evaluated for the hydrogen, oxygen and carbon atoms as well as for the methyl group at the level of time-dependent density functional theory with the B3LYP exchange-correlation functional employing a large Gaussian basis set. We find that the atomic or group contributions are not transferable among these three molecules.
| Original language | English |
|---|---|
| Journal | Molecular Physics |
| Volume | 112 |
| Issue number | 12 |
| Pages (from-to) | 1624-1632 |
| Number of pages | 9 |
| ISSN | 0026-8976 |
| DOIs | |
| Publication status | Published - 2014 |
Keywords
- atomic contributions
- chirality
- density functional theory
- dimethyl peroxide
- hydrogen peroxide
- methyl hydroperoxide
- optical rotatory power