dichloro-bis(N,N'-diisopropylbenzamidinato)(η5-pentamethylcyclopentadienyl)titanium (IV) | 206366-37-2

• 英文名称: dichloro-bis(N,N'-diisopropylbenzamidinato)(η5-pentamethylcyclopentadienyl)titanium (IV)
• CAS: 206366-37-2
• 化学式: C₂₃H₃₄Cl₂N₂Ti
• 分子量: 457.322
• InChiKey: QQOHZTRGXXRFRP-UHFFFAOYSA-L

计算性质

• 辛醇/水分配系数(LogP)：
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• 重原子数：
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• 可旋转键数：
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• 环数：
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• sp3杂化的碳原子比例：
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• 拓扑面积：
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• 氢给体数：
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• 氢受体数：
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反应信息

• 作为产物：
  描述：

  (五甲基环戊二烯基)三氯化钛(IV) 、 lithium N,N’-diisopropyl-benzamidinate 以 四氢呋喃 为溶剂， 以28%的产率得到dichloro-bis(N,N'-diisopropylbenzamidinato)(η5-pentamethylcyclopentadienyl)titanium (IV)
  参考文献：
  名称：

  Metallocene analogues containing bulky heteroallylic ligands and their use as new olefin polymerization catalysts

  摘要：

  A series of Ti and Zr metallocene analogues containing bulky benzamidinate ligands has been prepared and fully characterized, Treatment of TiCl4(THF)(2) or ZrCl4(THF)(2) with two equivalents of the appropriate benzamidinate anions affords the bis(benzamidinato) complexes [C6H5C(NC3H7)(2)](2)MCl2 (M = Ti (1), Zr (2)) and [C6H5C(NC6H11)(2)](2)MCl2 (M = Ti (3), Zr (4)). Tne zirconium complex 2 was structurally characterized by X-ray diffraction. In a similar manner the nonafluoromesityl derivative [(CF3)(3)C6H2C(NC6H11)(2)](2)ZrCl2 (5) was synthesized from ZrCl4(THF)(2) and Li[(CF3)(3)C6H2C(NC6H11)(2)]. Methylation of 4 with methyllithium yields the dimethyl complex [C6H5C(NC6H11)(2)](2)ZrMe2 (6). The mixed-ligand metallocene analogues [C6H5C(NC3H7)(2)](C5Me5)MCl2 (M = Ti (7), Zr (8)) and [C6H5C(NC6H11)(2)](C5Me5)TiCl2 (9) have been prepared by reacting (C5Me5)TiCl3 or (C5Me5)ZrCl3 with one equivalent of a lithium N, N "-dialkylbenzamidinate. The polymerization of ethylene and propylene has been studied by the catalytic precatalyst complexes 1 and 2 upon reaction of an excess of methylalumoxane to obtain the active cationic complexes. The polymerization activity of the complexes is comparable to other benzamidinate ancillary containing ligands although toward shorter amounts of time due to a competitive inhibition presumably obtained by a P-hydrogen elimination from the ligand. Polymerization activity is strongly dependent on catalyst and cocatalyst concentrations and on temperature. (C) 1998 Elsevier Science B.V.

  DOI：

  10.1016/s1381-1169(97)00209-4