Abstract

Isocyanides react readily with Ucp2(NEt2)2(cp = cyclopentadienyl) and U(C5Me5)2(NEt2)Cl giving iminoalkylamido insertion compounds: starting from Ucp2(NEt2)2 and an excess of isocyanide or form the monoinserted compound, a second insertion occurs, affording the highly symmetrical bis(iminoalkylamido) compounds; 1H n.m.r. data indicate the importance of a ‘carbenoid’ resonance hybrid and nitrogen lone-pair donation to the ‘carbenoid’ carbon atom.

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