Persistent Nitrogen-centered Free Radicals, N-(Arylthio)-3,5-di-t-butylphenylaminyls. Decomposition Reactions

DOI: 10.1246/bcsj.54.3215

Source and publish data:

Bulletin of the Chemical Society of Japan p. 3215 - 3216 (1981)

Update date:2022-09-26

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Authors:

Miura, Yozo

Yamamoto, Akifumi

Kinoshita, Masayoshi

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Article abstract of DOI:10.1246/bcsj.54.3215

N-(4-Chlorophenylthio)-3,5-di-t-butylphenylaminyl was decomposed in oxygen-free benzene, and the products were examined.On the basis of the results, the decomposition mechanism of the radical is described.

Full text of DOI:10.1246/bcsj.54.3215

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