Fischer Malte, Schmidtmann Marc, Beckhaus Rüdiger
Institut für Chemie, Fakultät für Mathematik und Naturwissenschaften, Carl von Ossietzky Universität Oldenburg, 26129 Oldenburg, Germany.
Acta Crystallogr E Crystallogr Commun. 2017 Nov 3;73(Pt 12):1823-1826. doi: 10.1107/S2056989017015560. eCollection 2017 Dec 1.
The crystal structure of a solvated zirconocene penta-fulvene complex with a bulky adamantyl-idene substitution pattern, namely (η,η-adamantyl-idene-penta-fulvene)bis-(η-cyclo-penta-dien-yl)zirconium(IV)-toluene--hexane (8/1/1), [Zr(CH)(CH)]·0.125CH·0.125CH, is reported. Reducing zirconocene dichloride with magnesium results in the formation of a low-valent zirconocene reagent that reacts readily with adamantyl-idene-penta-fulvene to give the aforementioned complex. Single crystal X-ray diffraction proves the dianion-like η:η binding mode of the fulvene ligand to the central Zr atom. The asymmetric unit contains four independent mol-ecules of [η:η-adamantyl-idene-penta-fulvene]bis-[(η)-cyclo-penta-dien-yl]zirconium(IV), together with half a mol-ecule of toluene disordered with half a mol-ecule of -hexane (the solvent mol-ecules have no direct influence on the complex). In each of the four complex mol-ecules, the central Zr atom has a distorted tetra-hedral coordination environment. The measured crystal consisted of two domains with a refined ratio of 0.77:0.23.
报道了一种具有庞大金刚烷基叉取代模式的溶剂化二茂锆五亚甲基配合物的晶体结构,即(η,η-金刚烷基叉-五亚甲基)双-(η-环戊二烯基)锆(IV)-甲苯-己烷(8/1/1),[Zr(CH)(CH)]·0.125CH·0.125CH。用镁还原二氯二茂锆会生成一种低价二茂锆试剂,该试剂能与金刚烷基叉-五亚甲基迅速反应生成上述配合物。单晶X射线衍射证明了亚甲基配体与中心Zr原子的类似双负离子的η:η配位模式。不对称单元包含四个独立的[η:η-金刚烷基叉-五亚甲基]双-[(η)-环戊二烯基]锆(IV)分子,以及半个甲苯分子和半个己烷分子无序排列(溶剂分子对配合物没有直接影响)。在四个配合物分子中的每一个中,中心Zr原子都具有扭曲的四面体配位环境。所测晶体由两个畴组成,精修比例为0.77:0.23。