Abstract
The tetrahydrido complex [WH4(κ4-P4)] (P4 = meso-o-C6H4(PPhCH2CH2PPh2)2) reacted with aliphatic nitriles AkCN at 80 °C in toluene to afford a series of the imido complexes, [W(NCH2Ak)(κ4-P4)] (2). Similar reactions with aromatic nitriles ArCN proceeded stepwise, leading to formation of the hydrido–alkylideneamido complexes [WH(N═CHAr)(κ4-P4)] (3) at the first stage and a subsequent isomerization into the imido complexes [W(NCH2Ar)(κ4-P4)] (4). Conversion of 3 into 4 was accelerated by electron-rich Ar groups such as p-CH3OC6H4, while it was completely inhibited when Ar was the considerably electron-deficient p-CF3C6H4. An X-ray crystallographic study on 2 (Ak = p-ClC6H4CH2) and 4 (Ar = p-tolyl) has disclosed a distorted-square-pyramidal coordination geometry, in which the apical position is occupied by the imido ligand with a WII–N triple bond. An almost linear WII═N═C linkage of 3 (Ar = p-tolyl) has also been determined. Complex 2 was capable of nitrene group transfer to isocyanide to produce carbodiimide.
Published Version
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