卡宾
反应性(心理学)
化学
过渡金属卡宾配合物
单重态
芳基
光化学
有机化学
催化作用
物理
激发态
医学
替代医学
病理
烷基
核物理学
作者
Jan Lorkowski,Patrick Yorkgitis,Melinda R. Serrato,Milan Gembický,Cezary Pietraszuk,Guy Bertrand,Rodolphe Jazzar
标识
DOI:10.1002/anie.202401020
摘要
Singlet carbenes are not always isolable and often even elude direct detection. When they escape observation, their formation can sometimes be evidenced by in situ trapping experiments. However, is carbene-like reactivity genuine evidence of carbene formation? Herein, using the first example of a spectroscopically characterized cyclic (amino)(aryl)carbene (CAArC), we cast doubt on the most common carbene trapping reactions as sufficient proof of carbene formation.
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