Moss Robert A, Tian Jingzhi, Sauers Ronald R, Krogh-Jespersen Karsten
Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, New Brunswick, NJ 08903, USA.
J Am Chem Soc. 2007 Aug 15;129(32):10019-28. doi: 10.1021/ja071799i. Epub 2007 Jul 21.
Contrary to implications in the literature, the sigma --> p absorptions of alkylchlorocarbenes (RCCl) are readily acquired by laser flash photolysis with UV-vis detection in solution at ambient temperature. Examples include RCCl with R = methyl, benzyl, t-butyl, 1-adamantyl, and cyclopropyl. These absorptions permit direct monitoring of carbene reactions and the formation of carbene-solvent complexes. The kinetics of the reactions of "free" and complexed MeCCl and PhCH2CCl were directly followed with tetramethylethylene and 1-hexene. Particularly effective complexation was provided by anisole and 1,3-dimethoxybenzene, which modulated the rates of intermolecular carbene additions. Computational studies are presented, which aid in understanding the carbene absorption spectra and the nature of the solvent complexes.
与文献中的暗示相反,烷基氯卡宾(RCCl)的σ→p吸收可以在室温下通过溶液中的紫外可见检测激光闪光光解轻松获得。实例包括R为甲基、苄基、叔丁基、1-金刚烷基和环丙基的RCCl。这些吸收允许直接监测卡宾反应以及卡宾-溶剂配合物的形成。用四甲基乙烯和1-己烯直接跟踪“游离”和络合的MeCCl和PhCH2CCl的反应动力学。苯甲醚和1,3-二甲氧基苯提供了特别有效的络合作用,它们调节了分子间卡宾加成的速率。本文还进行了计算研究,有助于理解卡宾吸收光谱和溶剂配合物的性质。