首页> 外文期刊>Inorganica Chimica Acta >Coordination chemistry of group 4 metal compounds with mixed-ligand, silyl-linked bis(amidinate) ligand and cyclopentadienyl
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Coordination chemistry of group 4 metal compounds with mixed-ligand, silyl-linked bis(amidinate) ligand and cyclopentadienyl

机译:具有混合配体,甲硅烷基连接的双(ami基)配体和环戊二烯基的第4组金属化合物的配位化学

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摘要

The synthesis and characterization of a class of group 4 metal derivatives based on the silyl-linked bis(amidinate) ligands [SiMe2{NC(Ph)N(2,6-R2Ph)Li}2] [L1 (R = H) and L2 (R = Me)] are described. The metal salts coordinated with cyclopentadienyl were used in order to increase the steric hindrance and lower the Lewis acidity of metal centers, which could prevent the N-ligands from rearranging. The tetradentate ligands L1 and L2 reacted with TiCl2(C5H5)2 to give compounds 1 and 2 in tridentate and bidentate bonding modes, respectively. Treatment of the ligand L1 with ZrCl3(C5H5) produced the half-sandwich zirconium complex 3. Reactions of the ligands with ZrCl2(C5H5)2 afforded zirconium compounds 4 and 5, demonstrating the same geometry as 1. Comparing these analogous molecular structures, it suggests that the coordination modes of the N-ligands are variable according to the properties of the metal centers as well as the bulky hindrance of the terminal groups on the seven-membered N–C–N–Si–N–C–N backbone.
机译:基于甲硅烷基连接的双(酰胺基)配体[SiMe2 {NC(Ph)N(2,6-R2Ph)Li} 2] [L1(R = H)和说明L2(R = Me)。使用与环戊二烯基配位的金属盐以增加空间位阻并降低金属中心的路易斯酸度,这可以防止N配体重排。四齿配体L1和L2与TiCl2(C5H5)2反应,分别以三齿和二齿键合模式得到化合物1和2。用ZrCl3(C5H5)处理配体L1产生了半夹心的锆配合物3。配体与ZrCl2(C5H5)2的反应得到了锆化合物4和5,其几何结构与1相同。比较这些相似的分子结构,建议根据金属中心的性质以及七元N–C–N–Si–N–C–N主链上端基的大位阻,N-配体的配位方式是可变的。

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