Nicholas J. Goodwin, William Henderson, Brian K. Nicholson, John Fawcett and David R. Russell
Removal of formaldehyde from the readily prepared ferrocenyl (R) hydroxymethylphosphine RCH2P(CH2OH)2 with one mole equivalent of Na2S2O5 gave the completely air-stable primary phosphine RCH2PH2 as a crystalline, sublimable solid. With [Mo(CO)6] both mono-, [Mo(CO)5(RCH2PH2)], and di-substituted, [Mo(CO)4(RCH2PH2)2], products are readily formed, and both were characterised by structure determinations. Reaction with [{RuCl2(p-cym)}2] (p-cym = p-cymene) resulted in bridge splitting to give the complex [RuCl2(p-cym)(RCH2PH2)]. With [Ru3(CO)12], RCH2PH2 reacted in analogous fashion to other primary phosphines, with two isolated products [Ru3(µ-H)2(CO)9(µ3-PCH2R)] and [Ru4(CO)11(µ4-PCH2R)2] containing cluster capping RCH2P phosphinidine ligands, the former characterised by a structure determination. Thus, the phosphine appears to show typical co-ordinative properties of a primary phosphine, but has the added advantage of being air-stable.