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2,3,9,10,16,17-hexakis(hexylthio)-23,24-bis(phenylethynyl)-29H,31H-phthalocyaninatocobalt(II) | 825635-22-1

中文名称
——
中文别名
——
英文名称
2,3,9,10,16,17-hexakis(hexylthio)-23,24-bis(phenylethynyl)-29H,31H-phthalocyaninatocobalt(II)
英文别名
cobalt(2+);6,7,15,16,24,25-hexakis(hexylsulfanyl)-33,34-bis(2-phenylethynyl)-2,11,20,29,37,39-hexaza-38,40-diazanidanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13,15,17,19(39),20,22,24,26,28,30(37),31(36),32,34-nonadecaene
2,3,9,10,16,17-hexakis(hexylthio)-23,24-bis(phenylethynyl)-29H,31H-phthalocyaninatocobalt(II)化学式
CAS
825635-22-1
化学式
C84H96CoN8S6
mdl
——
分子量
1469.13
InChiKey
XSPVYAXSIHIDEX-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

  • 作为产物:
    描述:
    1,2-dicyano-4,5-bis(hexylthio)benzene 、 cobalt(II) chloride 、 4,5-di(phenylethynyl)phthalonitrile1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下, 以 戊醇 为溶剂, 以8%的产率得到2,3,9,10,16,17-hexakis(hexylthio)-23,24-bis(phenylethynyl)-29H,31H-phthalocyaninatocobalt(II)
    参考文献:
    名称:
    Unsymmetrical phthalocyanines with alkynyl substituents
    摘要:
    The synthesis of unsymmetrically substituted metallophthalocyanines (M = Zn, Ni, Co) bearing two phenylethyl moieties and six alkythio substituents was achieved by co-cyclotetramerization of two different phthalonitrile derivatives, namely 4,5-di(hexyl-thio)phthalonitrile and 4,5-di(phenylethynyl)phthalonitrile in the presence of zinc, cobalt or nickel salts. In contrast to the totally alkyne substituted phthalocyanines, these partially alkyne-containing derivatives are more soluble and their Q band absorptions are red-shifted when compared with all alkylthio phthalocyanines. Electrochemical properties of the phthalocyanines were studied by cyclic voltammetry. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2004.09.021
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