作者:Adolphus A. H. Van Der Zeijden、Chris Mattheis、Roland Fröhlich
DOI:10.1002/cber.19971300910
日期:1997.9
The monofluorenyl zirconium complex [(.(5):.1-C13H8CH2CH2OMe)ZrCl2(μ-Cl)]2, (2), has been obtained bby reaction of the respective fluorenyl lithium derivative with ZrCl4 in diethyl ether. A single-crystal X-ray structural analysis shows that 2 is a chloride-bridged dimer, in which the fluorenyl ligand is bonded in a transitional tri- to pentahapto fashion. The relatively weak fluorenyl–zirconium bond
单芴基锆络合物[(。(5):. 1 -C 13 H 8 CH 2 CH 2 OMe)ZrCl 2(μ-Cl)] 2(2)已通过各自的芴基锂衍生物与ZrCl 4在乙醚中的溶液。单晶X射线结构分析表明2是氯桥联的二聚体,其中芴基配体以过渡的三至五结合方式键合。相对弱的芴基-锆键通过与芴基主链相连的醚侧链的分子内配位作用得以稳定。尽管如此,当2溶解在THF中时,二齿配体仍容易脱离。同时醚裂解产生螺[环丙烷-1,9'-芴]。