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Carbodicarbenes, Carbon(0) Derivatives, Can Dimerize
Author(s) -
Ruiz David A.,
Melaimi Mohand,
Bertrand Guy
Publication year - 2013
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.201300887
Subject(s) - carbene , allene , electrophile , ligand (biochemistry) , service (business) , computer science , transition (genetics) , carbon fibers , chemistry , metadata , fullerene , world wide web , organic chemistry , business , algorithm , biochemistry , receptor , composite number , catalysis , marketing , gene
Sometimes you have to be spontaneous : Increasing the electrophilicity of carbodicarbenes, by increasing the π‐accepting properties of the carbene moieties, can be done but at the expense of their stability. In contrast to the carbodibenzimidazol‐2‐ylidene, which can be stored at room temperature, the carbodibenzoxazol‐2‐ylidene spontaneously dimerizes above −20 °C. However, this bent allene (CCC angle calc : 135.5°) can be spectroscopically characterized and used as a ligand for transition metals.

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