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New organogold(I) complexes: Synthesis, structure, and dynamic behavior of the polynuclear organogold diphenylmethane and diphenylethane derivatives
Authors:Tat'yana V Baukova  Lyudmila G Kuz'mina  Natal'ya A Oleinikova  Dmitrii A Lemenovskii  Aleksander L Blumenfel'd
Institution:

aNesmeyanov Institute of Organoelement Compounds, Russian Academy of Science, Vavilov St. 28, Moscow 117813, Russia

bKurnakov Institute of General and Inorganic Chemistry, Russian Academy of Science, Leninskii pr. 31, Moscow 117907, Russia

cChemistry Department, Moscow State University, Leninskie Gory, Moscow 117234, Russia

Abstract:Two organogold derivatives of diphenylmethane and diphenylethane, Ph3PAu(o-C6H4)CH2(C6H4-o)AuPPh3 (1) and Ph3PAu(o-C6H4)(CH2)2(C6H4-o)AuPPh3 (2), have been synthesized by the reaction of ClAuPPh3 with Li(o-C6H4)CH2(C6H4-o)Li and Li(o-C6H4)(CH2)2(C6H4-o)Li respectively. The interaction of 1 with dppe results in the replacement of the two PPh3 groups to give a macrocyclic compound View the MathML source (3) that includes an Au cdots, three dots, centered Au bond. Compounds 1 and 2 react with one or two equivalents of Ph3PAu]BF4 to form new types of cationic complex CH2(C6H4-o)2(AuPPh3)3]BF4 (4), CH2(C6H4-o)2(AuPPh3)4](BF4)2 (5), and (CH2)2(C6H4-o)2(AuPPh3)4](BF4)2 (6). Complexes 1–6 have been characterized by X-ray diffraction studies, FAB MS, and IR as well as by 1H and 31P NMR spectroscopy. A complicated system of Au cdots, three dots, centered H-C agostic interactions, involving the bridging alkyl groups (—CH2— and CH2-CH2—) of diphenylmethane and diphenylethane ligands, has been found to occur in complexes 1–3 and 6.
Keywords:Agostic  Fluxionality  Crystal structure  Phenyl  Gold  Phosphine
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