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(R)-6,6'-bis(4''-vinylpyridyl)-2,2'-diethoxy-1,1'-binaphthalene | 785787-40-8

中文名称
——
中文别名
——
英文名称
(R)-6,6'-bis(4''-vinylpyridyl)-2,2'-diethoxy-1,1'-binaphthalene
英文别名
(S)-6,6'-bis(4''-vinylpyridyl)-2,2'-diethoxy-1,1'-binaphthalene;(S)-2,2'-diethoxy-1,1'-binaphthyl-6,6'-bis(4-vinylpyridine)
(R)-6,6'-bis(4''-vinylpyridyl)-2,2'-diethoxy-1,1'-binaphthalene化学式
CAS
785787-40-8;785787-42-0
化学式
C38H32N2O2
mdl
——
分子量
548.684
InChiKey
ZHWXRPNPDHPYDP-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):
    9.59
  • 重原子数:
    42.0
  • 可旋转键数:
    9.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.11
  • 拓扑面积:
    44.24
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为反应物:
    描述:
    (R)-6,6'-bis(4''-vinylpyridyl)-2,2'-diethoxy-1,1'-binaphthalene甲醇 为溶剂, 生成 [Cd((S)-2,2'-diethoxy-1,1'-binaphthyl-6,6'-bis(4-vinylpyridine)2(ClO4)2]*11C2H5OH*2H2O
    参考文献:
    名称:
    高度多孔的同手性金属有机骨架:溶剂交换诱导的单晶至单晶转变。
    摘要:
    DOI:
    10.1002/anie.200462711
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文献信息

  • Chiral Molecular Squares Based on Angular Bipyridines:  Self-Assembly, Characterization, and Photophysical Properties
    作者:Suk Joong Lee、Jason S. Kim、Wenbin Lin
    DOI:10.1021/ic0497937
    日期:2004.10.1
    Chiral molecular squares 1-12 based on [M(dppe)](2+) metallocorners (M = Pd or Pt, and dppe = bis-(diphenylphosphino)ethane) and new angular bipyridine bridging ligands derived from the 1,1'-binaphthyl framework were readily assembled and characterized by a variety of techniques including infrared, UV-vis, circular dichroism (CD), and NMR spectroscopy, and ESI mass spectrometry. All these chiral metallocycles are highly luminescent in solution at room temperature with quantum efficiency of 0.06-0.63. Interestingly, when equal molar enantiopure molecular squares of opposite handedness were mixed in solution, a new meso dimeric metallocycle with C-2 symmetry formed. This result indicates the lability of the M-pyridyl bonds in these metallocycles, which may hinder their applications in many enantioselective processes.
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