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(5-amino-10,20-diphenylporphinato)zinc(II) | 403830-48-8

中文名称
——
中文别名
——
英文名称
(5-amino-10,20-diphenylporphinato)zinc(II)
英文别名
——
(5-amino-10,20-diphenylporphinato)zinc(II)化学式
CAS
403830-48-8
化学式
C32H21N5Zn
mdl
——
分子量
540.942
InChiKey
LGUGXKLGVLPBGN-TVGBRLMZSA-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

  • 作为反应物:
    描述:
    辛胺(5-amino-10,20-diphenylporphinato)zinc(II)均苯四甲酸二酐N,N-二甲基甲酰胺 为溶剂, 以12%的产率得到N-[5-(10,20-diphenylporphirinato) zinc(II)]-N'-(octyl)pyromellitic diimide
    参考文献:
    名称:
    Synthesis, Excited-State Dynamics, and Reactivity of a Directly-Linked Pyromellitimide−(Porphinato)zinc(II) Complex
    摘要:
    N-[5-(10,20-Diphenylporphinato)zinc(ll)]-N'-(octyl)pyromellitic diimide (PZn-Pl), a meso-pyromellitimide-substituted (porphinato)zinc(II) compound, has been fabricated from the reaction of (5-amino-10,20-diphenylporphinato)zinc(II) with pyromellitic dianhydride in the presence of octylamine. Interrogation of the photoinduced charge separation (CS) and thermal charge recombination (CR) electron-transfer (ET) dynamics for PZn-Pl in CH2Cl2 via pumpprobe transient absorption spectroscopic methods shows that tau(cs) and tau(CR) are 770 and 5200 fs, respectively. These ET dynamics differ from those elucidated previously for closely related 5-quinonyl-substituted (porphinato)metal compounds, and derive from the fact that the low-lying excited states for PZn-PI are porphyrin-localized, possessing little charge-transfer character. The synthesis of N-{5-[15-(2-(triisopropylsilyl)ethynyl)-10,20-diphenylporphinato]zinc(ll)}-N'-(octyl)pyromellitic diimide demonstrates that PZn-Pl can be halogenated at its 15-meso-position and used subsequently as a substrate in metal-catalyzed cross-coupling reactions; the reactivity of PZn-Pl is unusual with respect to many directly linked donor-acceptor compounds in that it is stable to these oxidizing and reducing reaction conditions.
    DOI:
    10.1021/ic0108641
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