Reactions of co-ordinated ligands. Part 43. Alkyne linking reactions at dimetal centres. Synthesis and structures of [Mo2{µ-(σ,η3:η2:η3,σ-C8H4But4)}(η-C5H5)2], [Mo2{µ-(σ,η3:η3,σ-CHCHButC6H2But3)}(η-C5H5)2], and [FeMo(CO)2(C4Me2Ph2)(η-C5H5)2

Abstract

Addition of Na[Fe(CO)2(η-C5H5)] to a solution of [Mo(NCMe)(η2-ButC2H)2(η-C5H5)][BF4] in tetrahydrofuran affords the two complexes [Mo2{µ-(σ,η3:η2:η3,σ-C8H4But4)}(η-C5H5)2](1) and [Mo2{µ-(σ,η3:η3,σ-CHCHButC6H2But3)}(η-C5H5)2](2), structurally identified by n.m.r.spectroscopy and single-crystal X-ray crystallography. In (1) a C8 chain bridges the Mo ⋯ Mo vector [Mo(1)–Mo(2) 2.639(1)A], the chain beginning and ending with σ bonds to Mo(2). Carbons C(1), C(2), C(3) and C(6), C(7), C(8) each form an η3-allylic interaction with Mo(1) with C(4) and C(5) bonded as an η2-alkene to Mo(2). In contrast, complex (2) can be described as a 5-vinyl substituted C6‘fly-over’ complex where the C8 ligand bonds via a C–Mo σ bond to Mo(2) and an η4-diene-like interaction to Mo(1). One of the carbons, C(2), symmetrically bridges the Mo2 unit [Mo(1)–Mo(2) 2.705(5)A]. The mechanism of formation of these complexes is discussed. An attempt to extend these reactions to [Mo(NCMe)(η2-PhC2Me)2(η-C5H5)][BF4] and [Mo(NCMe)(η2-PhC2Ph)2(η-C5H5)][BF4] resulted in the formation of the dinuclear complexes [FeMo(CO)2(C4Me2Ph2)(η-C5H5)2](3) and [FeMo(CO)2(C4Ph4)(η-C5H5)2](4), the former being structurally characterised by X-ray crystallography.