L 3 C 3 P 3 : Tricarbontriphosphide Tricyclic Radicals and Cations Stabilized by Cyclic (alkyl)(amino)carbenes

Autor: Guy Bertrand, Yuanfeng Hou, Zhongshu Li, Yaqi Li, Hansjörg Grützmacher, Cheng-Yong Su, Alexander Hinz, Jeffrey Harmer
Přispěvatelé: Department of Chemistry, UCSD-CNRS Joint Research Chemistry Laboratory (UMI 3555), University of California [San Diego] (UC San Diego), University of California-University of California-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Zdroj: Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2018, 57 (1), pp.198-202. ⟨10.1002/anie.201710099⟩
ISSN: 1433-7851
1521-3773
Popis: Alkynes usually oligomerize to give rings with a conjugated π-electron system. In contrast, phosphaalkynes, R-C≡P, frequently give compounds with polycyclic structures, which are thermodynamically more stable than the corresponding π-conjugated isomers. The syntheses of the first CP tricyclic compounds are reported with either radical or cationic ground states stabilized by cyclic (alkyl)(amino)carbenes (CAACs). These compounds may be considered as examples of tricarbontriphosphide coordinated by carbenes and are likely formed via trimerization of the corresponding mono-radicals CAAC-CP. The mechanism for the formation of these tricarbontriphosphide radicals has been rationalized by a combination of experiments and DFT calculations.
Databáze: OpenAIRE