Investigations of Pyridine-2-thiol as a Ligand: Synthesis
and X-ray Structures of the Mixed Mo−Mn Dinuclear
Complex CpMoMn(CO)3(μ-CO)(μ-η2-pyS)(μ-η1-pyS), the
Electron-Deficient Trimolybdenum Cluster
Cp3Mo3(μ-CO)2(μ-S)(μ3-S)(μ-η2-NC5H4), and the
Mononuclear CpMo(CO)2(μ-η2-pyS)
posted on 2005-01-17, 00:00authored byNoorjahan Begum, Shariff E. Kabir, G. M. Golzar Hossain, A. F. M. Mahfuzur Rahman, Edward Rosenberg
The reaction of Mn2(CO)6(pyS)2 (1) with (CpMo(CO)3)2 (2) at 110 °C gives the heterodinuclear complex CpMoMn(CO)3(μ-CO)(μ-η2-pyS))(μ-η1-pyS) (3), the mononuclear molybdenum
complex CpMo(CO)2(μ-η2-pyS) (4), and the 46-electron trimolybdenum cluster Cp3Mo3(μ-CO)2(μ-S)(μ3-S)(μ-η2-NC5H4) (5). Compound 4 could also be prepared in high yield from the
reaction of 2 with pyridine-2-thiol at 110 °C. Compound 3 represents a rare example of a
Mo−Mn heterodinuclear complex containing a μ-η2-pyridine-2-thiolato, a μ-η1-pyridine-2-thiolato, and a cyclopentadienyl ligand. The 46-electron compound 5 represents a unique
example of a trimolybdenum compound containing three cyclopentadienyl ligands, an ortho-metalated pyridyl ligand, a capping sulfido, a bridging sulfido, and two semibridging CO
ligands. Curiously, although this complex is formally electron deficient, it is unreactive toward
two-electron donors. The structures of all the compounds have been unambiguously
established by single-crystal X-ray crystallography.