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| 138259-68-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
138259-68-4
化学式
C68H60N6O18S3
mdl
——
分子量
1345.45
InChiKey
LTPSFWOZXPHIRE-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):
    10.3
  • 重原子数:
    95
  • 可旋转键数:
    21
  • 环数:
    12.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    374
  • 氢给体数:
    9
  • 氢受体数:
    21

反应信息

  • 作为产物:
    描述:
    在 palladium on activated charcoal 氢气 作用下, 以 四氢呋喃溶剂黄146 为溶剂, 反应 48.0h, 以100%的产率得到
    参考文献:
    名称:
    Synthesis of metallomacrocyclophanes: Deduction of structure from electrospray ionization mass spectroscopy and molecular mechanics computations
    摘要:
    The synthesis of metallomacrocyclophanes 7-tos and 8, in which environmentally tunable ferric-catecholamide coordination bonds hold the cyclophane together, is described. W-vis spectroscopic studies of 7-tos and 8 display characteristics of ferric-tris(catecholamide) complexes, i.e. burgundy color (lambda(max) = ca. 490 nm)and high stability, at high pH, and 1:1 stoichiometry. Electrospray ionization mass spectra of 8 show prominent ions due to a monomeric 1:1 (ligand/metal) complex. Molecular mechanics calculations on 7 and 8 indicate that oar-isomeric configurations predominate, leaving a void in the metallomacrocyclophane interiors.
    DOI:
    10.1016/0040-4020(95)00287-i
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文献信息

  • Synthesis of trioxatricornan and derivatives. Useful keystones for the construction of rigid molecular cavities
    作者:Michael Lofthagen、Russell VernonClark、Kim K. Baldridge、Jay S. Siegel
    DOI:10.1021/jo00027a015
    日期:1992.1
    The synthesis of a new class of organic keystones for the development of macrocage structures is presented. These represent some of the most versatile building blocks for macrocage construction. The keystone structure developed herein can be interpreted as either a centrally alkylated [cd,mn]dibenzopyrene or a tris ortho-bridged triphenylmethane. We call this basic skeleton tricornan. Routes into both chiral (C3 and C1 symmetry) and achiral (C3-upsilon symmetry) derivatives are reported. The synthesis of derivatives of the trioxatricornan keystone, leading to two macrocage structures, is presented. The X-ray structures of cent-methyltrioxatricornan 7 and 2,6,10-tris(dimethylamino)-cent-methyltrioxatricornan (20) are discussed and compared to that of 1,1,1-triphenylethane. Empirical force field and AM1 calculations are compared to the X-ray structures and discussed. A general discussion on the keystone analogy is presented.
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