Vg. Albano et al., STRUCTURAL CHARACTERIZATION OF THE TRINUCLEAR CLUSTER COMPOUND [FE(CO)(4)(AUPPH(3))(2)] AND ISOLATION OF ITS PARENT ANION [FE(CO)(4)(AUPPH(3))](-), Inorganica Chimica Acta, 213(1-2), 1993, pp. 183-190
A re-investigation of the reaction of Au(PPh(3))Cl with [Fe(CO)(4)](2-
) has shown that the [Fe(CO)(4)(AuPPh(3))](-) monoanion and [Fe(CO)(4)
(AuPPh(3))(2)] are obtained in sequence by using a 1:1 and 2:1 molar r
atio, respectively. The complex [Fe(CO)(4)(AuPPh(3))(2)] crystallizes
in the monoclinic space group P2(1)/a, a=20.309(5), b=18.379(3), c=40.
737(6) Angstrom, beta=96.26(2)(0), Z=16, R=0.0526. There are four crys
tallographically independent but chemically equivalent molecules in th
e asymmetric unit. Each molecule consists of an Au2Fe triangle with th
e two Au atoms bearing a PPh(3) ligand and the iron atom bound to four
carbonyl groups. The feature of greatest interest in this molecule is
the Au-Au interaction whose length is found in the range 2.897-2.941(
1) Angstrom, quite different from that quoted from a previous study (3
.028(1) Angstrom).