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2,9-bis(2,2-dimethylpropoxy)-16,23-bis(2-(hydroxymethyl)-2-methylbutoxy)phthalocyanine | 130326-38-4

中文名称
——
中文别名
——
英文名称
2,9-bis(2,2-dimethylpropoxy)-16,23-bis(2-(hydroxymethyl)-2-methylbutoxy)phthalocyanine
英文别名
——
2,9-bis(2,2-dimethylpropoxy)-16,23-bis(2-(hydroxymethyl)-2-methylbutoxy)phthalocyanine化学式
CAS
130326-38-4
化学式
C54H62N8O6
mdl
——
分子量
919.136
InChiKey
LTWJNINNNGKVFM-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):
    11.29
  • 重原子数:
    68.0
  • 可旋转键数:
    14.0
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    186.3
  • 氢给体数:
    4.0
  • 氢受体数:
    12.0

反应信息

  • 作为产物:
    参考文献:
    名称:
    Syntheses of monometalated and unsymmetrically substituted binuclear phthalocyanines and a pentanuclear phthalocyanine by solution and polymer support methods
    摘要:
    Binuclear phthalocyanines in which two different phthalocyanine nuclei are covalently linked through five-atom bridges, derived from 2-ethyl-2-methylpropane-1,3-diol, are prepared. In the examples, one phthalocyanine ring is always substituted with neopentoxy substituents, while the other phthalocyanine ring is unsubstituted or contains tert-butyl substituents or a neopentoxy-substituted copper phthalocyanine, constituting a binuclear phthalocyanine in which only one ring is metalated. The precursor, 2-(2-(hydroxymethyl)-2-methylbutoxy)-9,16,23-trineopentoxyphthalocyanine was prepared in solution and also by solid-phase methods, using polymer-bound trityl chloride derived from a 1% divinylbenzene-co-styrene copolymer. A metal-free pentanuclear phthalocyanine, in which four phthalocyaninyl groups are covalently bound to the four benzo groups of a central phthalocyanine nucleus, is described and characterized by FAB mass spectroscopy. In some experiments some rare examples of demetalation of some zinc phthalocyanines are noted during phthalocyanine formation. A modified flash chromatography procedure proved to be useful for separating similarly substituted mononuclear phthalocyanines.
    DOI:
    10.1021/jo00001a019
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