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bis{2-[bis(4-ethyl-3-methylpyrrol-2-yl)methyl]phenyl} ether | 916844-12-7

中文名称
——
中文别名
——
英文名称
bis{2-[bis(4-ethyl-3-methylpyrrol-2-yl)methyl]phenyl} ether
英文别名
——
bis{2-[bis(4-ethyl-3-methylpyrrol-2-yl)methyl]phenyl} ether化学式
CAS
916844-12-7
化学式
C42H50N4O
mdl
——
分子量
626.885
InChiKey
BNIJKKXDERFYIA-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):
    10.63
  • 重原子数:
    47.0
  • 可旋转键数:
    12.0
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    72.39
  • 氢给体数:
    4.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    bis{2-[bis(4-ethyl-3-methylpyrrol-2-yl)methyl]phenyl} ether4,4'-diethyl-3,3'-dimethyl-5,5'-methanediyl-bis-pyrrole-2-carbaldehyde对甲苯磺酸邻四氯苯醌 作用下, 以 甲醇 为溶剂, 反应 49.0h, 以15%的产率得到bis[2-(2,8,13,17-tetraethyl-3,7,12,18-tetramethylporphyrin-5-yl)phenyl] ether
    参考文献:
    名称:
    Persistent Electron-Transfer State of a π-Complex of Acridinium Ion Inserted between Porphyrin Rings of Cofacial Bisporphyrins
    摘要:
    A free-base cofacial bisporphyrin, H(4)DPOx, forms a pi-complex with acridinium ion (AcH+) by pi-pi interaction in benzonitrile (PhCN). Formation of the H(4)DPOx-AcH+ pi-complex was probed by UV-vis and NMR spectroscopy. The binding constant between AcH+ and H(4)DPOx is determined as 9.7 x 10(4) M-1. Photoinduced electron transfer (ET) from the H(4)DPOx to the AcH+ moiety occurred efficiently in the d-complex to form the ET state (H(4)DPOx(center dot+)-AcH center dot). The ET state is successfully detected by laser flash photolysis. The lifetime of the ET state is 18 mu s in PhCN at 298 K, and the quantum yield of the ET state is 90%. The temperature dependence of the ET state lifetime has been examined in the range from 273 to 353 K. The ET state lifetime exhibited a large temperature dependence, and the linear plot of In(k(BET) T-1/2) vs T-1, in accordance with the Marcus equation, affords the ET reorganization energy (0.54 eV). As a result, a remarkably long-lived ET state has been attained at low temperature, and virtually no decay of the ET state was observed at 77 K. Such an extremely long-lived ET state is indeed detected by steadystate UV-vis absorption spectroscopy.
    DOI:
    10.1021/ja064678b
  • 作为产物:
    参考文献:
    名称:
    Persistent Electron-Transfer State of a π-Complex of Acridinium Ion Inserted between Porphyrin Rings of Cofacial Bisporphyrins
    摘要:
    A free-base cofacial bisporphyrin, H(4)DPOx, forms a pi-complex with acridinium ion (AcH+) by pi-pi interaction in benzonitrile (PhCN). Formation of the H(4)DPOx-AcH+ pi-complex was probed by UV-vis and NMR spectroscopy. The binding constant between AcH+ and H(4)DPOx is determined as 9.7 x 10(4) M-1. Photoinduced electron transfer (ET) from the H(4)DPOx to the AcH+ moiety occurred efficiently in the d-complex to form the ET state (H(4)DPOx(center dot+)-AcH center dot). The ET state is successfully detected by laser flash photolysis. The lifetime of the ET state is 18 mu s in PhCN at 298 K, and the quantum yield of the ET state is 90%. The temperature dependence of the ET state lifetime has been examined in the range from 273 to 353 K. The ET state lifetime exhibited a large temperature dependence, and the linear plot of In(k(BET) T-1/2) vs T-1, in accordance with the Marcus equation, affords the ET reorganization energy (0.54 eV). As a result, a remarkably long-lived ET state has been attained at low temperature, and virtually no decay of the ET state was observed at 77 K. Such an extremely long-lived ET state is indeed detected by steadystate UV-vis absorption spectroscopy.
    DOI:
    10.1021/ja064678b
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