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机构地区:[1]Department of Chemistry, Hebei University, Baoding, Hebei 071002, China [2]Department of Chemistry, Nankai University, Tianjin 300071, China
出 处:《Chinese Journal of Chemistry》2004年第10期1215-1218,共4页中国化学(英文版)
基 金:Project supported by the National Natural Science Foundation of China (No. 20072018).
摘 要:UV-Irradiation of 4-bromo-3-methyl-1-phenyl-4,5-dihydro-pyrazol-5-one (1) in the presence of various aromatic hydrocarbons gave different types of photoproducts; depending on the nature of the hydrocarbons via an electron-transfer mechanism. In the presence of naphthalene or phenanthrene a photochemical homocoupling reaction of I occurred to form 2 or 2 and 3, respectively.UV-Irradiation of 4-bromo-3-methyl-1-phenyl-4,5-dihydro-pyrazol-5-one (1) in the presence of various aromatic hydrocarbons gave different types of photoproducts; depending on the nature of the hydrocarbons via an electron-transfer mechanism. In the presence of naphthalene or phenanthrene a photochemical homocoupling reaction of I occurred to form 2 or 2 and 3, respectively.
关 键 词:photocoupling PYRAZOLONE EXCIPLEX electron-transfer mechanism
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