Semiempircal Local Spin: Theory and Implementation of the ZILSH Methanol for Predicting Heisenberg Exchange Constants of Polynuclear Transition Metal Complexes

摘要

The local spin formalism (Clark, A.E.; Davidson, E.R.J. Chem Phys 2001, 115, 7382-7392) for computing expectation values that appear in the Heisenberg spin model has been extended to semiempirical single determinant wave functions. An altnerative derivation of expectation values in restricted and unrestricted cases is given that takes advantage of the zero differential overlap (ZDO) approximation. A formal connection between single determinant wave functions (which are not in general spin eigenfunctions) and the Heisenberg spin model was established by demonstrating that energies of single determinants that are eigenfunctions of the local spin operators with eigenvalues corresponding to high-spin radical centers are given by the same Heisenberg coupling constants {J_AB} that describe the true spin states of the systemn. Unrestricted single determinant wave functions for transition metal complexes are good approximations of local spin eigenfunctions when the metal d orbitals are local in character and all unpaired electrons on each metal have the same spin (although spins on different metals might be reversed). Good aproximations of the coupling constants can then be extracted from local spin expectation valuese energies of the single determinant wave functions. Once the coupling constants are obtained, diagonalization of the Heisenberg spin Hamiltonian provides predictions of the energies and compositions of the spin states. A computational method is presented for obtaining coupling constants and spin-state energies in this way for polynuclear transition metal complexes using the intermediate neglect of differential overlap Hamiltonian parameterized for optical spectroscopy (INDO/S) in the ZINDO program. This method is referred to as ZILSH, derived from ZINDO, Davidson's local spin formalism, and the Heisenberg spin model. Coupling constants and spin ground states obtained for 10 iron complexes containing from 2 to 6 metals are found to agree well with experimental results in most cases. In the casae of the complex [Fe_6O_3(OAc)_9(OEt)_2(bpy)_2]~+, a priori predictions of the coupling constants yield a ground-state spin of zero, in agreement with variable-temperature magnetization data, and corroborate spin alignments proposed earlier on the basis of structural considerations. This demonstrates the potential of the ZILSH method to aid in understanding magnetic interactions in polynuclear transition metal complexes.