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卤代(吡啶鎓)卡宾的反应性。

Reactivity of halo(pyridinium)carbenes.

机构信息

Department of Chemistry, Dalhousie University, Halifax, Nova Scotia B3H 4J3, Canada.

出版信息

J Org Chem. 2009 Dec 4;74(23):9126-31. doi: 10.1021/jo901958g.

Abstract

The reactivity of chloro- and fluoro(N-methyl-3-pyridinium)carbenes was examined by laser flash photolysis, where the halo(pyridinium)carbenes formed ylides with pyridine, acetonitrile, and acetone. Although the halo(pyridinium)carbenes reacted within the time of the laser pulse, their relative reactivities with a series of alkenes could be obtained from quenching experiments by using carbene-pyridine ylides. Their relative order of reactivity with the alkenes and their poor overall selectivity showed that the halo(pyridinium)carbenes are strongly reactive electrophilic species. Computational studies demonstrated that the alkene (HOMO)-carbene (LUMO) interaction is predominant in halo(pyridinium)carbene-alkene reactions, supporting the electrophilic nature of these species.

摘要

通过激光闪光光解实验研究了氯代和氟代(N-甲基-3-吡啶鎓)碳烯的反应活性,其中卤代(吡啶鎓)碳烯与吡啶、乙腈和丙酮形成了叶立德。尽管卤代(吡啶鎓)碳烯在激光脉冲的时间内发生反应,但可以通过使用碳烯-吡啶叶立德进行猝灭实验来获得它们与一系列烯烃的相对反应活性。它们与烯烃的相对反应活性及其较差的整体选择性表明,卤代(吡啶鎓)碳烯是强反应性的亲电物种。计算研究表明,在卤代(吡啶鎓)碳烯-烯烃反应中,烯烃(HOMO)-碳烯(LUMO)相互作用占主导地位,支持这些物种的亲电性。

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