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Investigation of nitrogen-containing heterocyclic free radicals

XIV.Rate of dissociation of diaryl-β-naphthylimidazolyl radicals

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

Dimers of 4(5)-phenyl-5(4)-β-naphthyl-2-phenyl-substituted imidazolyl radicals were synthesized in order to study the effect of a β-naphthyl group on the stability of triaryl-imidazolyl radicals, and the rate constants and energies of activation for dissociation of the dimers were determined. The presence of a β-naphthyl group in the bistriarylimid-azolyl molecule facilitates its dissociation into radicals as compared with bistriphenyl-imidazolyl.

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Literature cited

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See [1] for communication XIII.

Translated from Khimiya Geterotsiklicheskikh Soedinnii, No. 9, pp. 1255–1257, September, 1971.

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Tanaseichuk, B.S., Bardina, A.A. & Khomenko, A.A. Investigation of nitrogen-containing heterocyclic free radicals. Chem Heterocycl Compd 7, 1180–1182 (1971). https://doi.org/10.1007/BF00510032

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  • DOI: https://doi.org/10.1007/BF00510032

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