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The stable carbene 1,2,3,5-tetramethylimidazol-2-ylidene forms an adduct with 3,5-dimethylborabenzene. This adduct 8 can readily be made from the carbene and 1-chloro-3,5-dimethyl-2-(trimethylsilyl)-1,2-dihydroborinine ( 6 ) as colorless crystals. The structure of 8 is closer to that of the anion in NMe 3 Ph(C 5 H 5 BMe) ( 9 ) than to the structures of known betainic adducts. There is no noticeable conjugation between the borabenzene and the imidazol-2-ylidene moieties.
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Zheng et al. (2000) studied this question.
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