Reiß Fabian, Reiß Melanie, Bresien Jonas, Spannenberg Anke, Jiao Haijun, Baumann Wolfgang, Arndt Perdita, Beweries Torsten
Leibniz-Institut für Katalyse e.V. an der Universität Rostock , Albert-Einstein-Str. 29a , 18059 Rostock , Germany . Email:
Abteilung für Anorganische Chemie , Institut für Chemie , Universität Rostock , Albert-Einstein-Straße 3a , D-18059 Rostock , Germany.
Chem Sci. 2019 Apr 23;10(20):5319-5325. doi: 10.1039/c9sc01002e. eCollection 2019 May 28.
The synthesis of an unusual 1-metalla-2,3-cyclobutadiene complex [-(ebthi)Ti(MeSiCSiMe)] (-ebthi = -1,2-ethylene-1,1'-bis(η-tetrahydroindenyl)), a formal metallacyclic analogue of a non-existent four-membered 1,2-cyclobutadiene, is described. By variation of the cyclopentadienyl ligand of the titanocene precursor it was possible to stabilise this highly exotic compound which selectively reacts with ketones and aldehydes to yield enynes by oxygen transfer to titanium. Analysis of the bonding and electronic structure of the metallacycle shows that the complex is best described as an unusual antiferromagnetically coupled biradicaloid system, possessing a formal Ti(iii) centre coordinated with a monoanionic radical ligand.
本文描述了一种不寻常的1-金属-2,3-环丁二烯配合物[-(ebthi)Ti(MeSiCSiMe)](-ebthi = -1,2-亚乙基-1,1'-双(η-四氢茚基))的合成,它是不存在的四元1,2-环丁二烯的一种形式上的金属环类似物。通过改变二茂钛前体的环戊二烯基配体,可以稳定这种高度奇特的化合物,它能与酮和醛选择性反应,通过向钛转移氧生成烯炔。对金属环的键合和电子结构分析表明,该配合物最好被描述为一种不寻常的反铁磁耦合双自由基体系,具有一个与单阴离子自由基配体配位的形式上的Ti(III)中心。