The preparation of multimetallic complexes using sterically bulky N-centred tripodal dialkyl phosphino ligands

Sterically bulky monodentate and bidentate phosphines have been widely used as ligands for metal complexation and catalyst formation. Bulky tridentate phosphine ligands are however much rarer and have not been widely investigated even though they may be considered attractive ligands for coordination chemistry studies and catalysis. Here we report the synthesis of two new N-centred tripodal phosphine ligands bearing bulky cyclohexyl and tert-butyl groups. The coordination chemistry of the cyclohexyl triphosphine ligand N(CH2PCy2)3 (4) was investigated and found to react with Mo and W hexacarbonyls preferentially forming bidentate metal tetracarbonyl complexes [Mo(CO)4{N(CH2PCy2)3-κ2P}] (6) and [W(CO)4{N(CH2PCy2)3-κ2P}] (7) over the expected facial capping tridentate complexes. The steric bulk of the cyclohexyl groups on the phosphorus atoms is sufficient to prevent the third arm of the ligand from coordinating and adopting the required geometry for facial coordination. This ‘steric control’ at the metal centre results in the third arm remaining freely available for further metal coordination. The coordination chemistry of this free phosphine arm on complexes 6 and 7 was investigated further and used to prepare a series of gold, platinum and silver multimetallic complexes. The X-ray crystal structures of the resulting mixed bi and trimetallic complexes [W(CO)4{N(CH2PCy2)3-κ2P}AuCl] (8), [[Mo(CO)4{N(CH2PCy2)3-κ2P}]2(μ-PtCl2)] (9) and [[W(CO)4{N(CH2PCy2)3-κ2P}]2(μ-Ag)]ClO4 (11) are reported.