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[((N,N-dimethyl-N',N'-bis(2-hydroxy-3-methyl-5-tert-butylbenzyl)ethylenediamine)(-2H))Ti(ethanolate)]2O | 1233478-15-3

中文名称
——
中文别名
——
英文名称
[((N,N-dimethyl-N',N'-bis(2-hydroxy-3-methyl-5-tert-butylbenzyl)ethylenediamine)(-2H))Ti(ethanolate)]2O
英文别名
[(trans-(Me2NCH2CH2N(CH2C6H2(CMe3)(Me)(O))2))Ti(OEt)]2O;[trans-(Me2NCH2CH2N(CH2C6H2(CMe3)(Me)(O))2)Ti(OEt)]2O
[((N,N-dimethyl-N',N'-bis(2-hydroxy-3-methyl-5-tert-butylbenzyl)ethylenediamine)(-2H))Ti(ethanolate)]2O化学式
CAS
1233478-15-3
化学式
C60H94N4O7Ti2
mdl
——
分子量
1079.19
InChiKey
PHBXOPKQWZJBMH-UHFFFAOYSA-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

计算性质

  • 辛醇/水分配系数(LogP):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    titanium(IV) isopropylate乙醇N,N-bis(2-hydroxy-3-methyl-5-tert-butylbenzyl)-N',N'-dimethylethylene-1,2-diamine 在 air 作用下, 以 乙醇 为溶剂, 以95%的产率得到[((N,N-dimethyl-N',N'-bis(2-hydroxy-3-methyl-5-tert-butylbenzyl)ethylenediamine)(-2H))Ti(ethanolate)]2O
    参考文献:
    名称:
    Synthesis and structure of diamine bis(phenolate) complexes containing the Ti(OEt)–O–Ti(OEt) function
    摘要:
    Reaction of diamine-bis(phenol) ligands containing a mixture of N-methyl and N,N'-dimethyl-N,N-bis(2-hydroxy-3,5-dimethylbenzyl)ethylenediamine, H(2)L(1) and H(2)L(3), with [Ti(OCHMe(2))(4) in absolute ethanol under reflux without exclusion of air and moisture gives [(L(1))Ti (OEt-O-Ti(OEt)(L(1))] (1). [(L(3))Ti(OEt)-O-Ti(OEt)(L(3))] (2) forms when the remaining solution containing [(L(3))Ti(OEt)(2)] (3) (characterised by X-ray crystallography) is hydrolysed with H(2)O. For the N-methyl and N,N'-dimethyl ligand mixture H(2)L(2) and H(2)L(4), which contain tert-butyl groups on the ortho-positions of the aryl rings, [(L(2))Ti(OEt)-O-Ti(OEt)(L(2))] (4) forms much more slowly and [(L(4))Ti(OEt)(2)] (5) does not hydrolyse when H(2)O is added. When the N-protonated ligand N,N-bis(2-hydroxy-3-methyl-5-tert-butylbenzyl)ethylenediamine, H(2)L(5), and H(2)L(4), which contain tert-butyl groups on the ortho-positions of the aryl rings, [(L(2))Ti(OEt)-O-Ti(OEt)(L(2))] (4) forms much more slowly and [(L(4))Ti(OEt)(2)] (5) does not hydrolyse when H(2)O is added. When the N-protonated ligand N,N-bis(2-hydroxy-3-methyl-5-tert-butylbenzyl)ethylenediamine, H(2)L(5), is used, rapid hydrolysis to two isomers of [(L(5))Ti(OEt-O-Ti(OEt)(L(5))] (6) occurs without addition of water. For N,N-bis(2-hydroxy-3,5-di-tert-butylbenzyl)ethylenediamine, H(2)L(6), hydrolysis to [(L(6))Ti(OEt)-O-Ti(OEt)(L(6))] (7) occurs slowly when H(2)O is added. For pendant NMe(2) ligand N,N-dimethyl-N',N'-bis(2-hydroxy-3-methyl-S-tert-butylbenzyl)ethylenediamine, H(2)L(7), the hydrolysis reaction readily gives [(L(7))Ti(OEt)-O-Ti(OEt)(L(7))] (8) for which an X-ray crystal structure was obtained. The ortho-tert-butyl ligand derivative H(2)L(8) formed a complex analysing as [(L(8))Ti(OEt)-O-Ti(OEt)(L(8))) (9) which could not be studied further due to insolubility. Pendant pyridine ligand N-(2-pyridylmethyl)-N,N-bis(2'-hydroxy-3'-methyl-T-tert-butylbenzyl)amine, H(2)L(9), apparently forms isomers of [(L(9))Ti(OEt)-O-Ti(OEt)(L(9))] and possibly [{(L(9))Ti(O)(2)] from [(L(9))Ti(OEt)(2)] (10). The ortho-tert-butyl ligand derivative H(2)L(10) formed [(L(10))Ti(OEt)-O-Ti(OEt)(L(10))] (11) for which an X-ray crystal structure was obtained. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2010.02.006
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