Mj. Almond et al., PHOTOCHEMICAL-SYNTHESIS AND CRYSTAL-STRUCTURE OF DIMETHYLPHOSPHINODITHIATOMANGANESE(I) TETRACARBONYL, [MN(CO)(4)(S(2)PME(2))], Polyhedron, 14(11), 1995, pp. 1433-1437
The new compound [Mn(CO)(4)(S(2)PMe(2)] (A) has been prepared by the p
hotochemical reaction of Mn-2(CO)(10) and Me(2)P(S)P(S)Me(2) in benzen
e solution. A single crystal X-ray diffraction study confirms that the
manganese atom in A is six-coordinate with a distorted octahedral arr
ay of atoms around the metal centre: the dithiophosphinate ligand adop
ts a chelating bidentate mode of coordination. The two P-S distances [
2.008(4) and 2.004(4) Angstrom] are equal within the limits of experim
ental error, as indeed are the two Mn-S distances [2.419(4) and 2.423(
4) Angstrom]. The ''bite'' S ... S distance is ca 3.196 Angstrom. The
Mn(CO)(4) moiety adopts local C-2v symmetry. The crystallographic data
are backed up by an IR spectroscopic study.