摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

[ZrCl2(N,N'-ethylenebis(5-chlorosalicylideneiminate))] | 866563-14-6

中文名称
——
中文别名
——
英文名称
[ZrCl2(N,N'-ethylenebis(5-chlorosalicylideneiminate))]
英文别名
——
[ZrCl2(N,N'-ethylenebis(5-chlorosalicylideneiminate))]化学式
CAS
866563-14-6
化学式
C16H12Cl4N2O2Zr
mdl
——
分子量
497.319
InChiKey
HSPGWHOQDAOEGW-QMCQXKLTSA-J
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

反应信息

  • 作为产物:
    描述:
    [ZrCl2(N,N'-ethylenebis(5-chlorosalicylideneiminate))(THF)]*0.5THF 以 甲苯 为溶剂, 生成 [ZrCl2(N,N'-ethylenebis(5-chlorosalicylideneiminate))]
    参考文献:
    名称:
    Preparation and structures of 6- and 7-coordinate salen-type zirconium complexes and their catalytic properties for oligomerization of ethylene
    摘要:
    A series of salen-type zirconium complexes of the general formula LZrCl2 (L = N,N '-ethylenebis(salicylideneiminate), 3a; N,N '-ethylenebis(3,5-di-tert -butylsalicylideneiminate), 3b; N,N '-ethylenebis(5-methoxysalicylidenciminate), 3e; N,N '-o-phethylenebis(5-chlorosalicylideneiminate), 3d; N,N '-ethylenebis(5-nitrosalicylideneiminate), 3e; N,N '-o-phenylenebis(salicylideneiminate), 4a; N,N '-o-phenylenebis(3,5-di-tert-butylsalicylideneiminate), 4b; N,N '-o-phenylenebis(5-methoxysalicylideneiminate), 4c; N,N '-o-phenylenebis(5-chloro-salicylideneiminate), 4d) were prepared. The crystal structures of 6- and 7-coordinate zirconium complexes 4b and [4b center dot OCMe2] were determined by X-ray crystallography, which reveals that a salen-type zirconium complex possesses a labile coordination site on the Zr center with a relatively stable framework and that the coordination and the dissociation of O-donor molecules occur readily at this site. The catalytic properties of 3(a-e) and 4(a-d) were studied for ethylene oligomerization in combination with Et2AlCl as co-catalyst. Complex 3c featuring a methoxy-substituted salen ligand displayed higher activity than its analogous precursors having chloro and nitro groups as substituents. The catalytic reactions by 3(a-e) and 4(a-d) gave C-4-C-10 olefins and low-carbon linear (alpha-olefins in good selectivity. (c) 2005 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2005.05.027
点击查看最新优质反应信息