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首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis, characterization, and styrene polymerization catalysis of pyridyl-functionalized indenyl rare earth metal bis(silylamide) complexes
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Synthesis, characterization, and styrene polymerization catalysis of pyridyl-functionalized indenyl rare earth metal bis(silylamide) complexes

机译:吡啶基官能化的茚基稀土金属双(甲硅烷基酰胺)配合物的合成,表征和苯乙烯聚合催化

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摘要

Amine elimination of rare earth metal tris(silylamide) complexes Ln[N(SiHMe_2)_2]_3(THF)_2 with 1 equiv of the pyridyl-functionalized indenyl ligand C_9H_7CMe _2CH_2C_5H_4N-α afforded the neutral mono-indenyl-ligated rare earth metal bis(silylamide) complexes (C _9H_6CMe_2CH_2C_5H 4N-α)Ln[N(SiHMe_2)_2]_2 (Ln = Sc (1), Y (2), Nd (3)) in 70-82% isolated yields. These complexes were characterized by elemental analysis, FT-IR, NMR, and X-ray single crystal structural diffraction. X-ray determination showed that the metal centers are coordinated by one indenyl ring, one nitrogen atom from the pendent pyridyl group, and two amide groups to form a distorted tetrahedral geometry. In the presence of excess Al~iBu_3 and on activation with 1 equiv of [Ph_3C][B(C_6F_5)_4] in toluene, 1-3 became active for syndiospecific polymerization of styrene in toluene at room temperature.
机译:用1当量的吡啶基官能化的茚基配体C_9H_7CMe_2CH_2C_5H_4N-α消除稀土金属三(甲硅烷基酰胺)络合物Ln [N(SiHMe_2)_2] _3(THF)_2的胺,得到中性的单茚基连接稀土金属bis (甲硅烷基)络合物(C _9H_6CMe_2CH_2C_5H4N-α)Ln [N(SiHMe_2)_2] _2(Ln = Sc(1),Y(2),Nd(3)),分离产率为70-82%。这些配合物通过元素分析,FT-IR,NMR和X射线单晶结构衍射进行表征。 X射线测定表明,金属中心由一个茚基环,一个来自侧基吡啶基的氮原子和两个酰胺基配位,形成扭曲的四面体几何形状。在过量的Al〜iBu_3的存在下,并在甲苯中用1当量的[Ph_3C] [B(C_6F_5)_4]活化后,在室温下1-3成为苯乙烯在甲苯中的间位聚合反应的活性。

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