SYNTHESIS AND ELECTROCHEMICAL STUDIES OF NEW FERROCENE-LABELED DINUCLEAR RHODIUM(II) COMPLEXES - CRYSTAL-STRUCTURES OF RH2(O2CME)2([(C6H4)PHP(C5H4)]FE(C5H5))2-(HO2CME)2] AND RH2(O2CME)2([(C6H4)PHP(C5H4)]2FE)-(HO2CME)].CH2CL2
F. Estevan et al., SYNTHESIS AND ELECTROCHEMICAL STUDIES OF NEW FERROCENE-LABELED DINUCLEAR RHODIUM(II) COMPLEXES - CRYSTAL-STRUCTURES OF RH2(O2CME)2([(C6H4)PHP(C5H4)]FE(C5H5))2-(HO2CME)2] AND RH2(O2CME)2([(C6H4)PHP(C5H4)]2FE)-(HO2CME)].CH2CL2, Journal of the Chemical Society. Dalton transactions, (11), 1993, pp. 1681-1688
The reaction of diphenylphosphinoferrocene and 1,1'-bis(diphenylphosph
ino)ferrocene with [Rh2(O2CMe)4(MeOH)2] (1:1 and 1:2 molar ratio respe
ctively) yields the monoadducts [Rh2(O2CMe)4{(Ph2PC5H4) Fe(C5H5)}] 1 a
nd [{Rh2(O2CMe)4(MeOH)}2{(Ph2PC5H4)2Fe}] 2. By thermal treatment of 1
in refluxing toluene-acetic acid (10:3) the monometallated product [Rh
2(O2CMe)3{[(C6H4)PhP(C5H4)]Fe(C5H5)}(HO2CMe)2] 3 was obtained in pract
ically quantitative yield. Compound 3 reacts with [Fe(C5H5)(C5H4PPh2)]
(1:1 molar ratio) giving the adduct )3{[(C6H4)PhP(C5H4)]Fe(C5H5)}{(Ph
2PC5H4)Fe(C5H5)}] 4, which reacts thermally in toluene-acetic acid (10
:3) yielding the doubly metallated product [Rh2(O2CMe)2{[(C6H4)PhP(C5H
4)]Fe(C5H5)}2(HO2CMe)2] 5 as a mixture of conformational isomers. An X
-ray determination of 5 has been carried out: space group Pbca (orthor
hombic), a = 18.065(3), b = 20.606(4), c = 26.242(5) angstrom, Z = 8,
and R = 0.038. The crystal structure shows that the two metallated pho
sphines are in a head-to-tail configuration. Thermal treatment of a mi
xture of [Rh2(O2CMe)4(MeOH)2] and [Fe(C5H4PPh2)2] (1:1 molar ratio) in
acetic acid yields the compound [Rh2(O2CMe)2{[(C6H4)PhP(C5H4)]2Fe}(HO
2CMe)].CH2Cl2 6 after purification and crystallization from a CH2Cl2-h
exane-acetic acid mixture. An X-ray diffraction investigation showed t
hat this compound crystallizes in space group P2(1)/c (monoclinic) wit
h a = 12.735(4), b = 16.811(5), c = 20.161(8) angstrom, beta = 95.17(4
)degrees, Z = 4 and R = 0.089. The two PPh2 fragments of the ferrocene
ligand act as bridging orthometallated ligands in a head-to-head conf
iguration. Two well defined oxidation processes were detected by cycli
c voltammetry for all the complexes in CH2Cl2 solution: the first one,
in the range 0.6-0.7 V, is due to the couple Fe2+-Fe3+ while the seco
nd one, in the range 0.9-1.32 V, is due to the couple Rh2(4+)-Rh2(5+).