SYNTHESIS OF S2-BRIDGED AND PF2O2-BRIDGED DINUCLEAR RUTHENIUM(IV) COMPLEX OBTAINED FROM THE REACTION OF DISULFIDE-BRIDGED RUTHENIUM(III) DIMER COMPLEX WITH DIOXYGEN AND WATER
K. Matsumoto et al., SYNTHESIS OF S2-BRIDGED AND PF2O2-BRIDGED DINUCLEAR RUTHENIUM(IV) COMPLEX OBTAINED FROM THE REACTION OF DISULFIDE-BRIDGED RUTHENIUM(III) DIMER COMPLEX WITH DIOXYGEN AND WATER, Bulletin of the Chemical Society of Japan, 70(6), 1997, pp. 1239-1244
Reaction of [{Ru(CH3CN)(3)[P(OMe)(3)](2)}(2)(mu-S-2)](PF6)(3) with a m
ixture of acetylene and O-2 gave a novel ruthenium(IV) dimer complex u
(IV)(PFO3)[P(OMe)(3)](2)}(2)(mu-S)(mu-PF2O2)(2)]. The newly formed bri
dging and terminal ligands PF2O2- and PFO32- are produced from the rea
ction of PF6- with trace amounts of H2O in the solvent. Although acety
lene is not incorporated in the final product, it is necessary to acce
lerate the reaction. Ruthenium(IV) complexes with S2- ligand are rare
and only two examples are previously known. The crystal of [{Ru(PFO3)[
P(OMe)(3)](2)}(2)(mu-S)(mu-PF2O2)(2)] is monoclinic, space group P2(1)
/n, a = 11.061(5), b = 20.764(4), c = 17.074(3) Angstrom, beta = 95.74
(2)degrees, V = 3901(1) Angstrom(3), and Z = 4. The bridging PF2O2- li
gand coordinates to Ru atoms with the two oxygen atoms, while the term
inal PFO32- ligand coordinates to a Ru atom with one of the oxygen ato
ms. The molecular structure is confirmed by P-31 and (FNMR)-F-19 spect
roscopy.