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锆茂氨基硼烷配合物中β-B-缔合异构体的表征

Characterization of beta-B-agostic isomers in zirconocene amidoborane complexes.

作者信息

Forster Taryn D, Tuononen Heikki M, Parvez Masood, Roesler Roland

机构信息

Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, AB, T2N 1N4 Canada.

出版信息

J Am Chem Soc. 2009 May 20;131(19):6689-91. doi: 10.1021/ja901460y.

Abstract

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.

摘要

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。

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