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首页> 外文期刊>Journal of Organometallic Chemistry >LII. Synthesis and characterization of bis- and mono-(eta(3)-allyl)neodymium(III) chloride, Nd(eta(3)-C3H5)(2)Cl center dot 1.5 THF and Nd(eta(3)-C3H5)Cl-2 center dot 2THF, for preparation of highly active and selective complex catalysts for 1,4-cis-
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LII. Synthesis and characterization of bis- and mono-(eta(3)-allyl)neodymium(III) chloride, Nd(eta(3)-C3H5)(2)Cl center dot 1.5 THF and Nd(eta(3)-C3H5)Cl-2 center dot 2THF, for preparation of highly active and selective complex catalysts for 1,4-cis-

机译:LII。合成和表征双氯化物和单(η(3)-烯丙基)钕(III),Nd(eta(3)-C3H5)(2)Cl中心点1.5 THF和Nd(eta(3)-C3H5) Cl-2中心点2THF,用于制备1,4-顺-

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摘要

The title complexes are obtainable by comproportionation reaction from Nd(eta(3)-C3H5)(3).Dioxan and NdCl3 . 2THF in the correspond ing molar ratio in tetrahydrofuran (THF) in very good yields. The characterization was done by elementary analysis, IR and H-1 NMR spectroscopy and for the bis(eta(3)-allyl) complex also by X-ray crystal structure analysis. In combination with methylaluminoxane (MAO) both complexes catalyze the 1.4-cis-polymerization of butadiene in toluene and heptane, respectively, with an extremely high activity and a selectivity up to 98%. The catalyst formation results from anion transfer to the Lewis-acid methylaluminoxane giving a cationic mono(eta(3)-allyl)neodymium(III) fragment, which is stabilized by coordinative interactions with the complex counter anion. (C) 1998 Elsevier Science S.A. [References: 32]
机译:可以通过Nd(eta(3)-C3H5)(3).Dioxan和NdCl3的歧化反应获得标题配合物。在四氢呋喃(THF)中具有相应摩尔比的2THF,收率很高。表征是通过元素分析,IR和H-1 NMR光谱进行的,对bis(eta(3)-烯丙基)配合物的表征也通过X射线晶体结构分析进行。与甲基铝氧烷(MAO)结合使用,两种络合物分别以极高的活性和高达98%的选择性催化丁二烯在甲苯和庚烷中的1.4-顺式聚合。催化剂的形成是由于阴离子转移到路易斯酸甲基铝氧烷中,产生了阳离子单(η(3)-烯丙基)钕(III)片段,该片段通过与络合抗衡阴离子的配位相互作用而得以稳定。 (C)1998 Elsevier Science S.A. [参考:32]

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