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Direct Observation of Carbamoylnitrenes
Authors:Hongmin Li  Huabin Wan  Zhuang Wu  Dingqing Li  Prof?Dr Didier Bégué  Prof?Dr Curt Wentrup  Prof?Dr Xiaoqing Zeng
Institution:1. The Key Lab of Health Chemistry and Molecular Diagnosis of Suzhou, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou, P.R. China;2. Institut des Sciences Analytiques et de Physico-Chimie pour l'Environnement et les Matériaux (IPREM), Université de Pau et des Pays de l'Adour, Pau, France;3. School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, Queensland, Australia
Abstract:As the prototype Curtius rearrangement reaction, carbamoyl azide decomposes into aminoisocyanate and molecular nitrogen. However, the key intermediate carbamoylnitrene was previously undetected, even though the decomposition of carbamoyl azides has been studied frequently since its discovery in the 1890s. Upon ArF laser (λ=193 nm) photolysis, the stepwise decomposition of the two simplest carbamoyl azides H2NC(O)N3 and Me2NC(O)N3, isolated in solid noble gas matrices, occurs with the formation of the corresponding carbamoylnitrenes H2NC(O)N and Me2NC(O)N. Both triplet species are characterized for the first time by combining matrix‐isolation IR spectroscopy and quantum‐chemical calculations. Subsequent visible‐light irradiations cause efficient rearrangement of these nitrenes into the respective aminoisocyanates.
Keywords:azides  Curtius rearrangement  IR spectroscopy  matrix isolation  nitrenes
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