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• W2008804702 abstract "Using the multireference configuration interaction method due to Grimme and Waletzke, combined with the atomic mean-field approximations for the efficient calculation of spin–orbit matrix elements, the g-tensors in second-order perturbation theory have been calculated for the main group radicals CO+, CN, BO, BS, MgF, AlO, O2, HCO, H2O+, NO2, CO2−, NF2, NO22−, O3−, ClO2, and H2CO+, and for the transition metal compounds ZnH, ZnF, and TiF3, using explicit sum-over-state expansions for up to 20 excited states. In most cases, a valence triple-zeta basis set with polarization functions has been employed. It is shown that the addition of diffuse functions to this basis set does not improve the g-tensor results, and in several instances leads to slower convergence of the sum-over-state expansion. The calculated g-tensors are in good agreement with experimental values, and with our previous multireference configuration interaction results available for 9 of the 19 radicals. Our results are shown to be equivalent to, or better than, values obtained by other theoretical methods. Examples of radicals for which g-tensor calculations presented problems in the past are AlO and TiF3. For AlO, we obtain Δg⊥=−1530 ppm (parts per million), compared with an experimental value of −1900 ppm in Ne matrix. Using the SVP (valence double-zeta plus polarization) basis set, Δg⊥ of TiF3 is calculated to be −115.3 ppt (parts per thousand), compared with experimental values of −111.9 and −123.7 ppt." @default.
• W2008804702 created "2016-06-24" @default.
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• W2008804702 date "2003-05-14" @default.
• W2008804702 modified "2023-10-09" @default.
• W2008804702 title "Efficient calculation of electron paramagnetic resonance g-tensors by multireference configuration interaction sum-over-state expansions, using the atomic mean-field spin–orbit method" @default.
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• W2008804702 doi "https://doi.org/10.1063/1.1569243" @default.
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