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机构地区:[1]College of Chemistry and Chemical Engineering, Henan Institute of Science and Technology [2]College of Resources and Environment, Henan Institute of Science and Technology [3]College of Chemistry and Chemical Engineering, Harbin Normal University
出 处:《Chinese Journal of Structural Chemistry》2012年第6期872-876,共5页结构化学(英文)
基 金:Supported by the Science Foundation of Education Department of Heilongjiang Province(12511142)
摘 要:Reduction of a series of N,N'-diaryl adipyl bis-azo compounds using hydrazine hydrate as reductant was investigated. The products were characterized by elemental analysis, IR and 1H NMR methods and confirmed to be N,N'-diaryl adipyl dihydrazine. The results show that hydrazine hydrate can selectively reduce azo bonds with other potential reducible bonds intact in the N,N'-diaryl adipyl bis-azo compounds. The yields are high up to 92% under mild reaction conditions. According to the previous reports, this reduction process was attributed to an indirect reduction mechanism through an intermediate diimide.Reduction of a series of N,N'-diaryl adipyl bis-azo compounds using hydrazine hydrate as reductant was investigated. The products were characterized by elemental analysis, IR and 1H NMR methods and confirmed to be N,N'-diaryl adipyl dihydrazine. The results show that hydrazine hydrate can selectively reduce azo bonds with other potential reducible bonds intact in the N,N'-diaryl adipyl bis-azo compounds. The yields are high up to 92% under mild reaction conditions. According to the previous reports, this reduction process was attributed to an indirect reduction mechanism through an intermediate diimide.
关 键 词:N N'-diaryl adipyl bis-azo compounds N N'-diaryl adipyl dihydrazine hydrazine hydrate selective reduction
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