Synthesis and fluxional character of derivatives of the type [HFe3(CO)10(µ2-CNR2)] and [HFe3(CO)9(µ3-CHNR)]
Abstract
Isonitrile substitution at room temperature of [PPN][HFe3(CO)11][PPN =(Ph3P)2N+] to yield the substituted anion [PPN][HFe3(CO)10(CNR)], followed by protonation or alkylation, gives complexes of the type [HFe3(CO)10(µ2-CNR1R2)](R1= alkyl, R2= Et,H) which exhibit resricted rotation about the C-N bond; at higher temperatures, products resulting from isonirile nisertion into the M-H bond may be observed.