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An Acyclic Imino‐Substituted Silylene: Synthesis, Isolation, and its Facile Conversion into a Zwitterionic Silaimine
Author(s) -
Inoue Shigeyoshi,
Leszczyńska Kinga
Publication year - 2012
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201203257
Subject(s) - silylene , ligand (biochemistry) , adduct , borane , chemistry , atom (system on chip) , crystallography , silicon , computer science , catalysis , organic chemistry , operating system , biochemistry , receptor
A new type of Si(II) : A novel silylene stabilized by a Cp* and an imidazolin‐2‐iminato ligand has been prepared using two different methods (see scheme). The X‐ray crystallographic structure shows that the silicon(II) center is coordinated to an η 2 ‐Cp* ligand and the nitrogen atom of an imidazolin‐2‐iminato ligand. This silylene easily reacts with B(C 6 F 5 ) 3 to give a stable borane adduct having a zwitterionic resonance structure.
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