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5,5',5'',12,12',12''-hexakis(3,5-di-tert-butylphenoxy)-9,9''-bis(2,6-diisopropylphenyl)-1H,1''H-[2,2':9',2''-teranthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline]-1,1',1'',3,3',3'',8,8',8'',10,10',10''(9H,9''H)-dodecaone | 1161933-73-8

中文名称
——
中文别名
——
英文名称
5,5',5'',12,12',12''-hexakis(3,5-di-tert-butylphenoxy)-9,9''-bis(2,6-diisopropylphenyl)-1H,1''H-[2,2':9',2''-teranthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline]-1,1',1'',3,3',3'',8,8',8'',10,10',10''(9H,9''H)-dodecaone
英文别名
——
5,5',5'',12,12',12''-hexakis(3,5-di-tert-butylphenoxy)-9,9''-bis(2,6-diisopropylphenyl)-1H,1''H-[2,2':9',2''-teranthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline]-1,1',1'',3,3',3'',8,8',8'',10,10',10''(9H,9''H)-dodecaone化学式
CAS
1161933-73-8
化学式
C180H178N6O18
mdl
——
分子量
2713.42
InChiKey
RLFVUQJAJXRVQN-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):
    45.87
  • 重原子数:
    204.0
  • 可旋转键数:
    20.0
  • 环数:
    29.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    279.66
  • 氢给体数:
    0.0
  • 氢受体数:
    18.0

反应信息

  • 作为产物:
    描述:
    1,7-(3',5'-di-t-butylphenoxy)perylene-3,4:9,10-tetracarboxyanhydrideN,N-二甲基甲酰胺 为溶剂, 反应 132.0h, 以17%的产率得到5,5',5'',12,12',12''-hexakis(3,5-di-tert-butylphenoxy)-9,9''-bis(2,6-diisopropylphenyl)-1H,1''H-[2,2':9',2''-teranthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline]-1,1',1'',3,3',3'',8,8',8'',10,10',10''(9H,9''H)-dodecaone
    参考文献:
    名称:
    Toward an n-Type Molecular Wire: Electron Hopping within Linearly Linked Perylenediimide Oligomers
    摘要:
    A series of linearly linked perylenediimide (PDI) dimers and trimers were synthesized in which the PDI pi systems are nearly orthogonal. These oligomers and several model compounds were singly reduced, and intramolecular electron hopping between the PDI molecules was probed by electron paramagnetic resonance (EPR) and electron nuclear double resonance (ENDOR) spectroscopy. When the functional groups attached to the ends of the oligomers were chosen to make each PDI molecule electronically equivalent, the single electron hops between the PDI molecules with rates that significantly exceed 10(7) s(-1). Rapid electron hopping between pairs of PDI molecules having orthogonal pi systems is unexpected and may expand the possible design motifs for organic electronic materials based on PDI.
    DOI:
    10.1021/ja902258g
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