Forster Taryn D, Tuononen Heikki M, Parvez Masood, Roesler Roland
Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, AB, T2N 1N4 Canada.
J Am Chem Soc. 2009 May 20;131(19):6689-91. doi: 10.1021/ja901460y.
The reaction of Cp(x)(2)ZrCl(2) (Cp(x) = Cp, Cp*) with ammonia borane in presence of n-butyllithium yielded Cp(2)Zr(Cl)NH(2)BH(3) and Cp(x)(2)Zr(H)NH(2)BH(3). These derivatives are isoelectronic with the ethyl zirconocene chloride and hydride, respectively, and feature a chelating amidoborane ligand coordinating through a Zr-N bond and a Zr-H-B bridge. In solution, each of the complexes consists of an equilibrium mixture of two isomers differing in the orientation of the amidoborane ligand with respect to the Zr-X bond (X = H, Cl), while in the solid state, only one isomer was observed. Such isomers have not been characterized for any metal complexes containing the isoelectronic beta-agostic ethyl ligand or any other agostic alkyl group.
Cp(x)(2)ZrCl(2)(Cp(x) = Cp、Cp*)与氨硼烷在正丁基锂存在下反应生成了Cp(2)Zr(Cl)NH(2)BH(3)和Cp(x)(2)Zr(H)NH(2)BH(3)。这些衍生物分别与乙基二氯锆和乙基氢锆等电子,并且具有通过Zr-N键和Zr-H-B桥配位的螯合氨基硼烷配体。在溶液中,每个配合物都由两种异构体的平衡混合物组成,这两种异构体在氨基硼烷配体相对于Zr-X键(X = H、Cl)的取向上有所不同,而在固态下,只观察到一种异构体。对于任何含有等电子β-邻位碳硼键乙基配体或任何其他邻位碳硼键烷基的金属配合物,尚未对这类异构体进行表征。