Abstract
The success of tris(pyrazolyl)borates has inspired the development of new scorpionate ligands that are based on other donor groups. These include borate ligands with thioimidazolyl, selenoimidazolyl, phosphine and N-heterocyclic carbene donors, ligands that provide a facial array of [S3], [Se3], [P3], and [C3] donors, respectively. These ligands are all more strongly donating than the tris(pyrazolyl)borates, with tris(carbene)borate ligands having the greatest donor strength. Despite the design similarities, strongly donating scorpionates differ in their topology and flexibility, donor properties and degradation pathways. The structural and electronic properties of these ligands are contrasted and related to their chemistry, particularly that of the transition metals. Bidentate congeners of all these ligands are also known and are briefly covered. The ability of strongly donating scorpionate ligands to stabilize metal ligand multiple bonds in late transition metal complexes is also briefly discussed.
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