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Method for the production of silylated fluoroethyl cyclopenadienyl ligands and silylated fluoroethyl cyclopenadienyl metal locenes

机译:制备甲硅烷基化的氟乙基环戊二烯基配体和甲硅烷基化的氟乙基环戊二烯基金属茂的方法

摘要

Processes for the production silyl bridged fluorenyl-cyclopentadienyl-metallocene compounds uses a mixture of an aromatic or aliphatic hydrocarbon and an alpha,beta-dialkoxy-alkane or aromatic compound. A process for the production of compounds of formula (1) comprises: (A) deprotonation of a compound of formula (2) with a base, (B) reaction of the deprotonated compound with a compound of formula (3) to form a compound of formula (4), (C) reaction of the compound of formula (4) with M+Cp- to form a compound of formula (5) and (D) reaction of the compound of formula (5) with a base and addition of LCl4. R1R2SiCl2 (3) R1, R2 = 1-20 C hydrocarbon; R3-R10 = H, halogen or 1-20C hydrocarbon; R11-R14 = H or 1-20C hydrocarbon; L = zirconium, hafnium or titanium; M = Li, Na, K, MgCl or MgBr; and Cp = cyclopentadienyl,. optionally substituted Step (A) is carried out in a mixture of an aromatic and/or aliphatic hydrocarbon and an alpha , beta -dialkoxy-alkane or alpha , beta -dialkoxyaromatic. An alkane is added after the deprotonation step and prior to step (B). Step (D) is carried out an aromatic and/or aliphatic hydrocarbon and a polar, aprotic solvent, with the exception of diethylether.
机译:生产甲硅烷基桥连的芴基-环戊二烯基-茂金属化合物的方法使用芳族或脂族烃与α,β-二烷氧基-烷烃或芳族化合物的混合物。制备式(1)化合物的方法包括:(A)将式(2)化合物与碱脱质子化,(B)使去质子化的化合物与式(3)化合物反应形成化合物式(4)的化合物,(C)使式(4)的化合物与M + Cp-反应形成式(5)的化合物,和(D)使式(5)的化合物与LCl4的碱和添加物。 R 1 R 2 SiCl 2(3)R 1,R 2 = 1-20C烃; R 3 -R 10 = H,卤素或1-20℃的烃; R 11 -R 14 = H或1-20C烃; L =锆,ha或钛; M = Li,Na,K,MgCl或MgBr;并且Cp =环戊二烯基。任选取代的步骤(A)在芳族和/或脂族烃与α,β-二烷氧基-烷烃或α,β-二烷氧基芳族化合物的混合物中进行。在去质子化步骤之后且在步骤(B)之前添加烷烃。步骤(D)是芳族和/或脂族烃和极性非质子溶剂,但乙醚除外。

著录项

  • 公开/公告号DE50006923D1

    专利类型

  • 公开/公告日2004-08-05

    原文格式PDF

  • 申请/专利权人 BASELL POLYOLEFINE GMBH;

    申请/专利号DE20005006923T

  • 发明设计人 BINGEL DR.;

    申请日2000-04-17

  • 分类号C07F7/08;C07F17/00;

  • 国家 DE

  • 入库时间 2022-08-21 22:42:10

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