In situ IR and NMR spectroscopic investigation of the formation and structure of protonated diacetylketene tetrachloroaluminate

S. Csihony, A. Bodor, J. Rohonczy, I. Horváth
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引用次数: 8

Abstract

In situ IR and multinuclear NMR are used to monitor the formation of protonated diacetylketene tetrachloroaluminate (1) in the reaction of acetyl chloride and AlCl3 in both dichloromethane and in 1-butyl-3-methylimidazolium chloride ([bmim]Cl). The existence of a fast equilibrium between two enolic forms of protonated diacetylketene (with [AlCl4]− as the counterion) is established. The structure of 1 is determined by the rarely used 13C{1H}–13C{1H} COSY experiment.
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质子化四氯铝酸二乙酰烯酮的形成和结构的原位红外和核磁共振研究
用原位红外光谱和多核核磁共振监测了乙酰氯和AlCl3在二氯甲烷和1-丁基-3-甲基咪唑氯([bmim]Cl)中的反应中质子化四氯铝酸二乙酰基烯(1)的生成。建立了质子化二乙酰烯酮(以[AlCl4]−为反离子)的两种烯醛形式之间的快速平衡。1的结构由很少使用的13C{1H} -13C {1H} COSY实验确定。
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