SYNTHESIS AND STRUCTURE OF FE-4(CO)(10)(MU(2)-CO)(MU(4)-TE)(2) AND FE-57 - MOSSBAUER-SPECTRA OF FE-3(CO)(9)(MU(3)-TE)(2) AND FE-4(CO)(10)(MU(2)-CO)(MU(4)-TE)(2)
Tf. Fassler et al., SYNTHESIS AND STRUCTURE OF FE-4(CO)(10)(MU(2)-CO)(MU(4)-TE)(2) AND FE-57 - MOSSBAUER-SPECTRA OF FE-3(CO)(9)(MU(3)-TE)(2) AND FE-4(CO)(10)(MU(2)-CO)(MU(4)-TE)(2), Journal of organometallic chemistry, 561(1-2), 1998, pp. 221-225
The compound Fe-4(CO)(10)(mu(2)-CO)(mu(4)-Te)(2) (1) has been prepared
by the reaction of Fe-3(CO)(9)Te-2 (2) and Fe-2(CO)(9) in toluene. Co
mpound 1 is also formed by UV light irradiation of 2 and Fe(CO), in TH
F. The structure of 1 was established by single-crystal analysis. Crys
tal data: orthorhombic, Pccn, a = 6.843(1), b = 15.814(1), c = 17.436(
1) Angstrom; V = 1887 Angstrom(3); Z = 4; T = 293 K, R-1 = 0.040. 1 co
nsists of a planar array of four iron atoms with a quadruply bridging
telluro ligand on each side of the plane. The shortest metal-metal bon
d contains a bridging carbonyl ligand, semi-bridging carbonyl ligands
bridge the two adjacent metal-metal bonds. Te-125-NMR investigations s
how a conversion from 1 to 2 within several hours. Fe-57 Mossbauer spe
ctra show two doublets for 1 and only one broadened doublet for 2. The
ratio of the intensities of the doublets of 1 is found close to unity
and confirms the existence of two equipopulated crystallographic site
s of iron. On the contrary, in the case of 2, the analysis of the spec
tra does not allow the expected correlation with the results of the cr
ystal structure determination. The same difficulty was previously enco
untered in the case of the isostructural selenide Fe-3(CO)(9)Se-2. (C)
1998 Elsevier Science S.A. All rights reserved.