Leibniz-Institut für Katalyse e. V. an der Universität Rostock, Albert-Einstein-Strasse 29A, 18059 Rostock, Germany.
Chemistry. 2012 Aug 20;18(34):10546-53. doi: 10.1002/chem.201201114. Epub 2012 Jul 11.
A study regarding coordination chemistry of the bis(diphenylphosphino)amide ligand Ph(2) P-N-PPh(2) at Group 4 metallocenes is presented herein. Coordination of N,N-bis(diphenylphosphino)amine (1) to [(Cp(2) TiCl)(2) ] (Cp=η(5) -cyclopentadienyl) generated [Cp(2) Ti(Cl)P(Ph(2) )N(H)PPh(2) ] (2). The heterometallacyclic complex [Cp(2) Ti(κ(2) -P,P-Ph(2) P-N-PPh(2) )] (3 Ti) can be prepared by reaction of 2 with n-butyllithium as well as from the reaction of the known titanocene-alkyne complex [Cp(2) Ti(η(2) -Me(3) SiC(2) SiMe(3) )] with the amine 1. Reactions of the lithium amide [(thf)(3) Li{N(PPh(2) )(2) }] with [Cp(2) MCl(2) ] (M=Zr, Hf) yielded the corresponding zirconocene and hafnocene complexes [Cp(2) M(Cl){κ(2) -N,P-N(PPh(2) )(2) }] (4 Zr and 4 Hf). Reduction of 4 Zr with magnesium gave the highly strained heterometallacycle [Cp(2) Zr(κ(2) -P,P-Ph(2) P-N-PPh(2) )] (3 Zr). Complexes 2, 3 Ti, 4 Hf, and 3 Zr were characterized by X-ray crystallography. The structures and bondings of all complexes were investigated by DFT calculations.
本文介绍了双(二苯基膦基)酰胺配体 Ph(2) P-N-PPh(2) 在第 4 族茂金属配合物中的配位化学。N,N-双(二苯基膦基)胺(1)与[(Cp(2) TiCl)(2) ](Cp=η(5) -环戊二烯基)配位生成[Cp(2) Ti(Cl)P(Ph(2) )N(H)PPh(2) ](2)。杂金属环戊二烯基钛配合物[Cp(2) Ti(κ(2) -P,P-Ph(2) P-N-PPh(2) )](3Ti)可以通过 2 与正丁基锂反应以及通过已知的钛烯炔配合物[Cp(2) Ti(η(2) -Me(3) SiC(2) SiMe(3) )]与胺 1 反应来制备。锂酰胺[(thf)(3) Li{N(PPh(2) )(2) }]与[Cp(2) MCl(2) ](M=Zr,Hf)反应生成相应的锆和铪配合物[Cp(2) M(Cl){κ(2) -N,P-N(PPh(2) )(2) }](4Zr 和 4Hf)。用镁还原 4Zr 得到高度应变的杂金属环戊二烯基[Cp(2) Zr(κ(2) -P,P-Ph(2) P-N-PPh(2) )](3Zr)。通过 X 射线晶体学对 2、3Ti、4Hf 和 3Zr 进行了表征。通过 DFT 计算研究了所有配合物的结构和键合。