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(2-vinylpyridine)Al(C6F5)3 | 1632067-27-6

中文名称
——
中文别名
——
英文名称
(2-vinylpyridine)Al(C6F5)3
英文别名
(2-vinylpyridine)Al(C6F5)3;(2-VP)Al(C6F5)3
(2-vinylpyridine)Al(C6F5)3化学式
CAS
1632067-27-6
化学式
C25H7AlF15N
mdl
——
分子量
633.295
InChiKey
MXDCEHDJTFLXPU-UHFFFAOYSA-N
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

  • 作为反应物:
    参考文献:
    名称:
    Synthesis of Pyridine- and 2-Oxazoline-Functionalized Vinyl Polymers by Alane-Based Frustrated Lewis Pairs
    摘要:
    Reported herein is the first example of polymerization of polar vinyl monomers bearing the C=C-C=N functionality by Frustrated Lewis pairs (FLPs). In particular, FLPs based on Al(C6F5)(3) and N-heterocyclic carbenes rapidly convert 2-vinyl pyridine and 2-isopropenyl-2-oxazoline into medium to high molecular weight, Nfunctionalized vinyl polymers. Activated monomer-alane adduct 1 and initiated zwitterionic intermediate 2 have been isolated and structurally characterized, providing strong evidence for the proposed bimolecular, activated monomer polymerization mechanism.
    DOI:
    10.1055/s-0033-1341248
  • 作为产物:
    描述:
    2-乙烯基吡啶 、 tris(pentafluorophenyl)aluminum*(toluene)0.5 以 甲苯 为溶剂, 以100%的产率得到(2-vinylpyridine)Al(C6F5)3
    参考文献:
    名称:
    Synthesis of Pyridine- and 2-Oxazoline-Functionalized Vinyl Polymers by Alane-Based Frustrated Lewis Pairs
    摘要:
    Reported herein is the first example of polymerization of polar vinyl monomers bearing the C=C-C=N functionality by Frustrated Lewis pairs (FLPs). In particular, FLPs based on Al(C6F5)(3) and N-heterocyclic carbenes rapidly convert 2-vinyl pyridine and 2-isopropenyl-2-oxazoline into medium to high molecular weight, Nfunctionalized vinyl polymers. Activated monomer-alane adduct 1 and initiated zwitterionic intermediate 2 have been isolated and structurally characterized, providing strong evidence for the proposed bimolecular, activated monomer polymerization mechanism.
    DOI:
    10.1055/s-0033-1341248
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