Tetra-kis(di-cyclo-hexyl-amido)-zirconium(IV)

IUCrdata. 2020 Sep 4;5(Pt 9):x201145. doi: 10.1107/S2414314620011451. eCollection 2020 Sep.

Abstract

The reaction of ZrCl4 with three equivalents of LiNCy2 (Cy is cyclo-hex-yl) resulted in the formation of tris-(di-cyclo-hexyl-amido)-zirconium chloride and the title compound, [Zr(C12H22N)4]. The latter is isotypic with its cerium(IV) analogue and crystallizes with three independent mol-ecules in the asymmetric unit. One mol-ecule is located about a twofold rotation axis, and the other two on fourfold inversion axes. In each mol-ecule, the ZrIV atom has a distorted tetra-hedral coordination environment. The crystal under investigation was twinned by inversion in a 1:1 ratio.

Keywords: amide; crystal structure; isotypism; zirconium.

Grants and funding

Funding for this research was provided by: Deutsche Forschungsgemeinschaft (GRK No. 2226).