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A Carbene-Stabilized Boryl-Phosphinidene.

Samir Kumar SarkarSubrata KunduMohd NazishJohannes KretschRegine Herbst-IrmerDietmar StalkeParameswaran ParvathyPattiyil ParameswaranHerbert W Roesky
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2022)
Herein, the synthesis and characterization of the carbene-stabilized boryl phosphinidenes 1-3 are reported. Compounds 1-3 are obtained by reacting Me-cAAC=PK (Me 2 -cAAC=dimethyl cyclic(alkyl)(amino)carbene) and dihaloaryl borane in toluene. All three compounds were characterized by X-ray crystallography. Quantum mechanical studies indicated that these compounds have two lone pairs on the P center viz., an σ-type lone pair and a "hidden" π-type lone pair. Hence, these compounds can act as double Lewis bases, and the basicity of the π-type lone pair is higher than the σ-type lone pair.
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