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[(MeCH(C6H2(t-Bu)2O)2)Ti(μ2-O-i-Pr)2(O-i-Pr)Na(THF)2] | 1204302-17-9

中文名称
——
中文别名
——
英文名称
[(MeCH(C6H2(t-Bu)2O)2)Ti(μ2-O-i-Pr)2(O-i-Pr)Na(THF)2]
英文别名
——
[(MeCH(C6H2(t-Bu)2O)2)Ti(μ2-O-i-Pr)2(O-i-Pr)Na(THF)2]化学式
CAS
1204302-17-9
化学式
C47H81NaO7Ti
mdl
——
分子量
829.026
InChiKey
OHVMVFUXAXBSIW-UHFFFAOYSA-L
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:
    四氢呋喃titanium(IV) isopropylate 、 sodium hydride 、 2,2′-亚乙基双(4,6-二叔丁基酚) 以 tetrahydrofuran 为溶剂, 以30%的产率得到[(MeCH(C6H2(t-Bu)2O)2)Ti(μ2-O-i-Pr)2(O-i-Pr)Na(THF)2]
    参考文献:
    名称:
    Synthesis and Structural Studies of Heterobimetallic Alkoxide Complexes Supported by Bis(phenolate) Ligands: Efficient Catalysts for Ring-Opening Polymerization of l-Lactide
    摘要:
    A series of heterobimetallic titanium(IV) complexes [LTi(O(i)Pr)(mu-O(i)Pr)(2)Li(THF)(2)], [LTi(O(i)Pr)(mu-O(i)Pr)(2)Na(THF)(2)], [LTi(mu-O(i)Pr)(2)Zn(O(i)Pr)(2)], and [LTi(mu-O(i)Pr)(2)Mg(O(i)Pr)(2)] (where L = bidentate bisphenol ligands) have been synthesized and characterized including a structural determination of [L(1)Ti(mu(2)-O(i)Pr)(2)(O(i)Pr)Li(THF)(2)] (1a). These complexes were investigated for their utility in the ring-opening polymerization (ROP) of l-lactide (LA). Polymerization activities have been shown to correlate with the electronic properties of the substituent within the bisphenol ligand. In contrast to monometallic titanium initiator 1e, all the heterobimetallic titanium initiators (Ti-Li, Ti-Na, Ti-Zn, and Ti-Mg) show enhanced catalytic activity toward ring-opening polymerization (ROP) of l-LA. In addition, the use of electron-donating methoxy or methylphenylsulfonyl functional ligands reveals the highest activity. The bisphenol bimetallic complexes give rise to controlled ring-opening polymerization, as shown by the linear relationship between the percentage conversion and the number-average molecular weight. The polymerization kinetics using 2c as an initiator were also studied, and the experimental results indicate that the reaction rate is first-order with respect to both monomer and catalyst concentration with a polymerization rate constant, k = 81.64 M(-1) min(-1).
    DOI:
    10.1021/ic901938e
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