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Synthesis and Properties of Triazol-5-one Substituted Phthalocyanines by Microwave Irradiation

机译:微波辐射三唑-5-酮取代酞菁的合成及性能

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摘要

Triazol-5-one substituted phthalocyanines were prepared quickly by the reaction of 4-nitrophthalonitrile with anhydrous metal salts in DBU (1,8-diazabicyclo[5,4,0]undec-7-ene) and DMAE (dimethylaminoethanol) by microwave irradiation.Microwave yields were higher than those of the conventional synthesis methods.All of these complexes axe insoluble in polar solvents such as ethanol,ethyl acetate and chloroform.The characterization of the compounds was accomplished by elemental analysis,1H NMR (for I and II),13C NMR (for I and II),IR and UV-Vis spectral data.In addition,the structure of the starting material (I) was determined by single crystal diffraction.
机译:通过4-硝基邻苯二甲腈与无水金属盐在DBU(1,8-二氮杂双环[5,4,0] undec-7-ene)和DMAE(二甲基氨基乙醇)中的反应快速制备三唑-5取代的酞菁。微波收率高于常规合成方法,所有这些络合物均不溶于极性溶剂如乙醇,乙酸乙酯和氯仿中。化合物的表征通过元素分析,1 H NMR(I和II)完成13 C NMR(I和II),IR和UV-Vis光谱数据。另外,原料(I)的结构通过单晶衍射确定。

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