Cobalt‐Mediated [3+1] Fragmentation of White Phosphorus: Access to Acylcyanophosphanides
Sebastian Hauer, Thomas M. Horsley Downie, Gábor Balázs, Kai Schwedtmann, Jan J. Weigand, Robert Wolf
Abstract
Abstract Despite the accessibility of numerous transition metal polyphosphido complexes through transition‐metal‐mediated activation of white phosphorus, the targeted functionalization of P n ligands to obtain functional monophosphorus species remains challenging. In this study, we introduce a new [3+1] fragmentation procedure for cyclo ‐P 4 ligands, leading to the discovery of acylcyanophosphanides and ‐phosphines. Treatment of the complex [K(18c‐6)][(Ar*BIAN)Co(η 4 ‐P 4 )] ([K(18c‐6)] 3 , 18c‐6=[18]crown‐6, Ar*=2,6‐dibenzhydryl‐4‐isopropylphenyl, BIAN=1,2‐bis(arylimino)acenaphthene diimine) with acyl chlorides results in the formation of acylated tetraphosphido complexes [(Ar*BIAN)Co(η 4 ‐P 4 C(O)R)] (R= t Bu, Cy, 1‐Ad, Ph; 4 a – d ). Subsequent reactions of 4 a – d with cyanide salts yield acylated cyanophosphanides [RC(O)PCN] − ( 9 a – d − ) and the cyclo ‐P 3 cobaltate anion [(Ar*BIAN)Co(η 3 ‐P 3 )(CN)] − ( 8 − ). Further reactions of 4 a – d with trimethylsilyl cyanide (Me 3 SiCN) and isocyanides provide insight into a plausible mechanism of this [3+1] fragmentation reaction, as these reagents partially displace the P 4 C(O)R ligand from the cobalt center. Several potential intermediates of the [3+1] fragmentation were characterized. Additionally, the introduction of a second acyl substituent was achieved by treating [K(18c‐6)] 9b with CyC(O)Cl, resulting in the first bis(acyl)monocyanophosphine (CyC(O)) 2 PCN ( 10 ).