Journal of Organometallic Chemistry p. 381 - 390 (1988)
Update date:2022-08-24
Topics:
Vicente, Jose
Chicote, M.Teresa
Bermudez, M.Dolores
Sanchez-Santano, Maria J.
Jones, Peter G.
The reaction ( 1 1) between [Au(2-C6H4CH2NMe2)Cl2] and [HgPh2] gives [Au(2-C6H4CH2NMe2)(Ph)Cl]. From this complex, the neutral [Au(2-C6H4CH2NMe2)(Ph)X] (X : Br, I, CN, MeCO2) complexes are obtained by reaction with X- salts. Cationic complexes [Au(2-C6H4CH2NMe2)(Ph)L]ClO4 (L : pyridine, tetrahydrothiophene) are obtained by treatment of [Au(2-C6H4CH2-NMe2)(Ph)Cl] with ClO4- and the relevant ligand L. The complex [Au(2-C6H4-CH2NMe2)(Ph)Cl] crystallizes in two modifications, both with three independent molecules in the asymmetric unit. The AuN and AuCl bonds are long, consistent with the appreciable trans influence of the C-donor ligands. The molecules differ somewhat in the orientation of the rings.
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