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Ti2O(N,N'-bis(salicylidene)ethylenediamine(-2H))(p-tert-butylbenzoate) | 1355451-47-6

中文名称
——
中文别名
——
英文名称
Ti2O(N,N'-bis(salicylidene)ethylenediamine(-2H))(p-tert-butylbenzoate)
英文别名
——
Ti2O(N,N'-bis(salicylidene)ethylenediamine(-2H))(p-tert-butylbenzoate)化学式
CAS
1355451-47-6
化学式
C54H54N4O9Ti2
mdl
——
分子量
998.804
InChiKey
DSIAFFWGWJLFDY-RTPTWWPESA-H
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:
    [TiO(1,2-OC6H4CH=NCH2CH2N=CHC6H4O-1,2)] 、 对叔丁基苯甲酸 以 further solvent(s) 为溶剂, 生成 Ti2O(N,N'-bis(salicylidene)ethylenediamine(-2H))(p-tert-butylbenzoate)
    参考文献:
    名称:
    Reactions of {TiO(salen)}n [salen=N,N′-bis(salicylidene)ethylenediamine] in aromatic aldehydes and ketones
    摘要:
    Polymeric {TiO(salen)}(n) prepared from {Ti(OCHMe2)(2)(acac)(2)} and salen-H-2 in MeOH and with an apparent chain structure, is mostly insoluble but dissolves when strongly heated in aromatic aldehydes or ketones, depositing the insoluble form again on cooling. p-Tolualdehyde performed differently, giving a red solution from which insoluble red crystals were deposited. X-ray crystallography showed the complex was [{Ti(salen)(O2CC6H4Me-4)-O-Ti(salen)(O2CC6H4Me-4)]. Solvent (1) (solvent = p-tolualdehyde or p-toluic acid) containing a Ti-O-Ti bridge. Reaction of (TiO(salen)), with p-tert-butylbenzoic acid in the presence of excess p-tolualdehyde gave [{Ti(salen)(O2CC6H4CMe3-4)-O-Ti(salen)(O2CC6H4CMe3-4)]. 4-CH3C6H4CHO (2) for which an X-ray crystal structure determination indicated similar connectivity around the metal as for (1). (TiO(salen)) heated strongly in isobutyrophenone (PhCOCHMe2) also gave red crystals which X-ray analysis showed structural similarity to (1) and (2) but incorporating a PhCO2-ligand. {TiO(salen)) heated in acetophenone gave a product which X-ray analysis showed was a dioxo-bridged dimer (4) in which C-C bond formation had occurred on one side of each salen ligand. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2011.11.013
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