首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Solar and ultraviolet N-dealkylation of N,N-diemthylaminobenzylidene malonic acid derivatives via photoexcited polycyclic nitrioaromatic compounds
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Solar and ultraviolet N-dealkylation of N,N-diemthylaminobenzylidene malonic acid derivatives via photoexcited polycyclic nitrioaromatic compounds

机译:N,N-二甲基氨基亚苄基丙二酸衍生物通过光激发的多环硝基芳族化合物的太阳和紫外线N-脱烷基作用

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摘要

Broadband irradiation of N,N-dimethylaminobenzylidene malonic acid derivatives in benzene solution with polycyclic nitroaromatic compunds,namely 1-nitronaphthalene,9-nitroanthracene and 1-nitropyrene leads to mono-alkylated products predominant,accompanied by the corresponding photoreduction products of the nitroaromatics,lower conversion was obsewrved in acetonitrile concomitant with 2-4% of the mono-alkylated products,however,no conversion was observed in methanol as solvent.The structures of the products were assigned based on IR,~1H-,~(13)C NMR and mass spectra,elemental analyses and comparison with authentic samples.
机译:用多环硝基芳族化合物(即1-硝基萘,9-硝基蒽和1-硝基py)对苯溶液中的N,N-二甲基氨基亚苄基丙二酸衍生物进行宽带辐照,以单烷基化产物为主,伴随着相应的硝基芳族化合物的光还原产物,较低乙腈与2-4%的单烷基化产物同时发生转化,但是在甲醇为溶剂中未观察到转化。产物的结构基于IR,〜1H-,〜(13)C NMR进行分配质谱,元素分析和与真实样品的比较。

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