Primary dependence of 7-aryl-2,5-di-t-butyl-1,3,5-cycloheptatriene valence tautomerism on the π-acceptor strength of the 7-aryl substituent |
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Authors: | Kenichi Takeuchi Hiroshi Fujimoto Kunio Okamoto |
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Institution: | Department of Hydrocarbon Chemistry, Faculty of Engineering, Kyoto University, Sakyo-ku, Kyoto 606, Japan |
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Abstract: | 13C NMR studies showed that the population of the norcaradiene form of the title systems containing p-CH3O, H, and p-CF3 on the 7-aryl group increases in this order. The result is consistent with the prediction from the π-acceptor strength of the aryl group estimated by INDO calculations. |
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