Chemistry of 2H-azaphosphirene complexes, part 21 - Bond-selective nitrileinsertion into the 2H-azaphosphirene ring system as induced by tetracyanoethylene

Competitive reactions of 2H-azaphosphirene metal complexes la-e (M = Cr, Mo , W) with 1-piperidinonitrile and tetracyanoethylene in toluene have been o bserved at elevated temperatures. For the case of complex Ic, the Delta (5) -1,2-azaphospholene complex 2c (as main product) and the 2H-1,4,2-diazaphos phole complex 3c (as by-product) were separated from the product mixture. A t ambient temperature and using 1-piperidinonitrile as solvent, bond and re gioselective insertion of 1-piperidinonitrile into the P-N bond of 2H-azaph osphirene metal complexes la-e (M = Cr, Mo, W) has been achieved in the pre sence of tetracyanoethylene (TCNE), yielding 2H-1,4,2-diazaphosphole metal complexes 3a - c; analogous reactions in benzo- or acetonitrile afforded th e 2H-1,4,2-diazaphosphole tungsten complexes 3d, e. A preliminary study wit h the 2H-azaphosphirene tungsten complex Ic and 1-piperidinonitrile as solv ent has revealed that substoichiometric amounts of TCNE (0.3 equiv) induce approximately 70% conversion of complex Ic. NMR data of the complexes 2c an d 3a-e and the X-ray structure of complex 3c are discussed.