Author:
McDowell C. A.,Paulus K. F. G.
Abstract
The alkali metal hyperfine interaction in ion pairs of sodium and potassium cations with the radical anions of some methyl-substituted pyrazines and pyridines has been investigated. The electrostatic, electronic, and steric interactions which influence the metal hyperfine splitting are discussed in detail. It is proposed that the variation of the observed hyperfine splitting is due, in some cases, to steric effects, but in the series of m-xylene, 3,5-dimethylpyridine, and 2,6-dimethylpyrazine, the variation is caused by a change in the energy of electronic excitations from the anion to the cation.The results of molecular orbital calculations of the spin densities in tetramethylpyrazine and 3,5-dimethylpyridine are compared with experiment and found to give reasonable agreement.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
33 articles.
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1. References;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
2. On the adiabatic dynamics of paramagnetic ion pairs;Applied Magnetic Resonance;1992-10
3. Radical cations and anions of pyrazines: an electron paramagnetic resonance study;Journal of the Chemical Society, Perkin Transactions 2;1992
4. Caractéristiques des spectres de résonance paramagnétique électronique des radicaux formés à partir des tétrahydro-1,2,3,4 et octahydro-1,2,3,4,6,7,8,9 phénazine;Spectrochimica Acta Part A: Molecular Spectroscopy;1986-01
5. Electron transfer to complex ligands. Radical anions and organomagnesium radical complexes of 2,2'-bipyridines and 1,10-phenanthrolines;Journal of the American Chemical Society;1982-07