Vilanova Sean P, Alayoglu Pinar, Heidarian Mohammad, Huang Patrick, Walensky Justin R
Department of Chemistry, University of Missouri, Columbia, MO, 65211, USA.
Department of Chemistry, California State University East Bay, Hayward, CA, 94542, USA.
Chemistry. 2017 Nov 27;23(66):16748-16752. doi: 10.1002/chem.201704782. Epub 2017 Nov 7.
The complexes (C Me ) Th(EHTipp) , (E=P or As; Tipp=2,4,6-triisopropylphenyl), provide a ligand framework that results in facile access to rare Th-E multiple bonds. The reaction of (C Me ) Th(EHTipp) with KN(SiMe ) , proceeds cleanly to the desired bridging phosphinidiide or arsinidiide complex, [{(C Me ) Th(μ -ETipp)(μ -EHTipp)}K] under ambient conditions. In the absence of a chelating agent, the potassium cation of one monomeric unit interacts with the aryl ring of a second monomer to form a bridged dimer. In the presence of 2,2,2-cryptand, the terminal phosphinidene complex, [(C Me ) Th=PTipp(PHTipp)][K(2,2,2-cryptand)] is isolated. Using X-ray crystallographic analysis, we have determined these complexes display the shortest Th-P and Th-As bond lengths reported.
配合物(CMe)Th(EHTipp)(E = P或As;Tipp = 2,4,6 - 三异丙基苯基)提供了一种配体框架,使得能够轻松获得罕见的Th - E多重键。(CMe)Th(EHTipp)与KN(SiMe)反应,在环境条件下可顺利生成所需的桥连次膦基或次胂基配合物[{(CMe)Th(μ - ETipp)(μ - EHTipp)}K]。在没有螯合剂的情况下,一个单体单元的钾阳离子与第二个单体的芳环相互作用形成桥连二聚体。在2,2,2 - 穴醚存在下,可分离得到末端次膦基配合物[(CMe)Th = PTipp(PHTipp)][K(2,2,2 - 穴醚)]。通过X射线晶体学分析,我们确定这些配合物具有已报道的最短的Th - P和Th - As键长。