Antiferromagnetic complexes involving metalmetal bonds IV. Synthesis, molecular structure and magnetic properties of the heterotrinuclear cluster, (C5H5Cr)2(μ²-SCMe3)(μ³-S)2Fe(CO)3, with direct and indirect exchange between Cr^III and Fe^I centers

The photochemical reaction between the antiferromagnetic complex (C5H5-CrSCMe3)2S (I) (containing a CrCr bond 2.689 A long) and Fe(CO)5 results in the elimination of two carbonyl groups and one tert-butyl radical to give (C5H5Cr)2(μ2-SCMe3)(μ3-S)2 · Fe(CO)3 (III). As determined by X-ray diffraction, III contains a CrCr bond of almost the same length as in I (2.707 A), together with one thiolate and two sulphide bridges. The latter are also linked with the Fe atom of the Fe(CO)3 moiety (average FeS bond length 2.300 A). Fe also forms a direct bond, 2.726 A long, with one of the Cr atoms, whereas its distance from the other Cr atom (3.110 A) is characteristic for non-bonded interactions. Complex III is antiferromagnetic, the exchange parameter, −2J, values for CrCr, Cr(1)Fe and Cr(2)…Fe are 380, 2600 and 170 cm−1, respectively. The magnetic properties of III are discussed in terms of the “exchange channel model”. The contributions from indirect interactions through bridging ligands are shown to be insignificant compared with direct exchange involving metalmetal bonds. The effects of steric factors and of the nature of the M(CO)n fragments on the chemical transformations of (C5H5CrSCMe3)2S · M(CO)n are discussed.