Pyridine adducts of arylbismuth(III) halides

Abstract

A range of bismuth trihalide and arylbismuth(III) halide complexes with pyridine ligands has been prepared and structurally characterised. The complex [BiI₃(py)₃] (py = pyridine) is octahedral with the iodide and pyridine ligands arranged in a mer configuration. A seven-co-ordinate complex [BiCl₃(py)₄] is also described. The compounds [BiCl₂Ph(4-Mepy)₂] (4-Mepy = 4-methylpyridine), [BiBr₂Ph(4-Mepy)₂], [BiBr₂Ph(4-Bu^tpy)₂] (4-Bu^tpy = 4-tert-butylpyridine) and [BiI₂Ph(4-Bu^tpy)₂] all have a five-co-ordinate, square-based pyramidal bismuth centre in which the phenyl group occupies the apical position with two trans halides and two trans pyridine ligands residing in the basal plane. In the solid state these moieties are dimerised through a pair of weak asymmetric halide bridging interactions. The complexes [BiBr₂Ph(py)₂] and [BiI₂Ph(4-Mepy)₂] have similar monomeric units but in the former case these are weakly associated into polymeric chains rather than dimers whereas, for the latter, dimers are formed through a single bridging iodide. In the structure of the ionic compound [4-Bu^tpyH][BiCl₃Ph(4-Bu^tpy)] the [BiCl₃Ph(4-Bu^tpy)]^– anion is monomeric with a square-based pyramidal structure in which the phenyl group is in an apical site whilst the three chlorides and 4-Bu^tpy ligand occupy the basal positions. An example of a diphenylbismuth halide complex is seen in the structure of [BiIPh₂(4-Mepy)], the monomeric unit of which contains a four-co-ordinate bismuth centre with a geometry based on an equatorially vacant trigonal bipyramid in which the two phenyl groups are equatorial and the iodide and 4-methylpyridine ligand are axial. A weak association into polymeric chains occurs through long Bi  · · ·  I interactions approximately trans to one phenyl group. All compounds are discussed in terms of their structure and bonding and compared with related materials previously characterised.

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