Chemistry of nitrosoimines. XIV. Photolysis of 5-nitrosoimino-4-phenyl-3-phenylimino-1,2,4-thiadiazolidine.
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概要
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Photolysis of 5-nitrosoimino-4-phenyl-3-phenyliraino-1,2,4-thiadiazolidine proceeded through π-π<SUP>*</SUP> excitation and gave phenylcyanamide and 5-imino-4-phenyl-3-phenylimino-1,2,4-thiadiazolidine as primary products. It was found that other products were produced by the reactions of the primary products. The formation mechanisms have been discussed briefly.
- 公益社団法人 日本化学会の論文
著者
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Akiba Kin-ya
Department Of Chemistry Faculty Of Science Hiroshima University
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Inamoto Naoki
Department Of Chemistry Graduate School Of Science The University Of Tokyo
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Tsuchiya Tohru
Department of Chemistry, Faculty of Science, The University of Tokyo
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Tsuchiya Tohru
Department of Applied Chemistry, Faculty of Science and Technology, Keio University
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Fukawa Isaburo
Department of Chemistry, Faculty of Science, The University of Tokyo
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Inamoto Naoki
Department of Chemistry and Research Centre for Spectrochemistry, Faculty of Science, The University of Tokyo
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