A Polarographic Study of Aryl-substituted Tetra-aza- and Hexa-aza-pentalenes in Dimethylformamide
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概要
- 論文の詳細を見る
The polarographic reduction potentials of aryl-substituted 1,2,4,5-tetra-aza- and 1,2,3,4,5,6-hexa-aza-pen-talenes were shown to be approximately governed by the numbers of nitrogen atoms and aryl-substituents. Such effect of nitrogen atoms was discussed in terms of the orbital energies of parent azapentalenes obtained by HMO calculations.
- 公益社団法人 日本化学会の論文
著者
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Matsumoto Akira
Department Of Aeronautics And Astronautics Faculty Of Engineering Kyushu University
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Yoshida Masayuki
Department Of Applied Genetics Medical Research Institute Tokyo Medical And Dental University
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Simamura Osamu
Department of Chemistry Faculty of Science The University of Tokyo
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Lee Joung
Department of Chemistry, Faculty of Science, The University of Tokyo
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