Diamagnetic 8-amidoquinoline and 8-(trialkylsilylamido)quinoline complexes of divalent nickel and zinc

Abstract

Transamination of Zn[N(SiMe 3) 2] 2 with 8-(triisopropylsilylamino) ( 1a) and 8-(tert-butyldimethylsilylamino)quinoline ( 1b) yields monomeric heteroleptic bis(trimethylsilyl)amido zinc 8-(trialkylsilylamido)quinoline ( 2a, 2b). The reaction of Zn[N(SiMe 3) 2] 2 with 8-aminoquinoline leads to the formation of heteroleptic dimeric 8-amidoquinoline zinc bis(trimethylsilyl)amide ( 3). This compound shows fluxionality on the NMR time scale due to a transannular trans– cis isomerization process and also a strong temperature dependency of the ratio of these two isomers. Variation of the stoichiometry allows the synthesis and isolation of homoleptic zinc bis(8-amidoquinoline) ( 4) with the zinc atoms in a distorted tetrahedral environment. The metallation of 8-aminoquinoline with (tmeda)NiMe 2 yields diamagnetic nickel bis(8-amidoquinoline) ( 5) with a nickel center showing a distorted square planar coordination sphere. Dinuclear zinc complexes are accessible employing tetra-dentate di(8-aminoquinolyl)diphenylsilane ( 6). The metallation of 6 with dimethylzinc yields dimeric zinc di(8-amidoquinolyl)diphenylsilane ( 7) with tetrahedrally coordinated zinc atoms. A comparison of the molecular structures of 1a, 2b, 3, 4, 5, 6, and 7 shows nearly no dependency of the structural data of the quinolyl unit on the substitution pattern of the amino function. The metal–nitrogen bond lengths depend on the coordination numbers of the metal and the nitrogen atoms (terminal or bridging position) as well as the electrostatic attraction between the metal cations and the amino bases.