A VIBRATIONAL MODEL FOR THE COORDINATE BOND IN SULFOXIDE COMPLEXES

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1971

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Ohio State University

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Abstract

Effective force constants for the M-O and S-O stretching vibrations of a number of quasi-oetahedral dimethyl-and tetramethylene-sulfoxide complexes have been derived using a 13-atomic model of S. symmetry for the complex. With the aid of certain approximations and assumptions, these force constants have been analyzed in terms of ion: dipole, ion:induced-dipole, and covalent interactions. The covalent contribution can be related to the number of vacancies in the 3d subshell of the coordinating ion. Results suggest that the $t_{2g}$ orbitals are about 80 as effective as $e_{g}$ orbitals in contributing to the M-O force constant.

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Author Institution: Department of Chemistry, University of New Hampshire

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