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Pentaarylcyclopentadienyl Iron, Cobalt, and Nickel Halides

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NIAID Data Ecosystem2026-03-09 收录
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https://figshare.com/articles/dataset/Pentaarylcyclopentadienyl_Iron_Cobalt_and_Nickel_Halides/3085360
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The preparation of new stable half-sandwich transition metal complexes, having a bulky cyclopentadienyl ligand C5(C6H4-4-Et)5 (CpAr1) or C5(C6H4-4-nBu)5 (CpAr2), is reported. The tetrahydrofuran (THF) adduct [CpAr1Fe­(μ-Br)­(THF)]2 (1a) was synthesized by reacting K­[CpAr1] with [FeBr2(THF)2] in THF, and its molecular structure was determined by X-ray crystallography. Complex 1a easily loses its coordinated THF molecules under vacuum to form the solvent-free complex [CpAr1Fe­(μ-Br)]2 (1b). The analogous complexes [CpAr1Co­(μ-Br)]2 (2), [CpAr1Ni­(μ-Br)]2 (3), and [CpAr2Ni­(μ-Br)]2 (4) were synthesized from CoBr2 and [NiBr2­(1,2-dimethoxyethane)]. The mononuclear, low-spin cobalt­(III) and nickel­(III) complexes [CpAr2MI2] (5, M = Co; 6, M = Ni) were prepared by reacting the radical CpAr2 with NiI2 and CoI2. The complexes were characterized by NMR and UV–vis spectroscopies and by elemental analyses. Single-crystal X-ray structure analyses revealed that the dimeric complexes 1a, 1b, and 3 have a planar M2Br2 core, whereas 2 and 4 feature a puckered M2Br2 ring.
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2016-03-15
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