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[7,8,12,13,17,18-hexapropyl-[1,2,5]selenadiazolo[3,4-q]porphyrazinato]zinc(II) | 888014-95-7

中文名称
——
中文别名
——
英文名称
[7,8,12,13,17,18-hexapropyl-[1,2,5]selenadiazolo[3,4-q]porphyrazinato]zinc(II)
英文别名
Zn[pz(Pr)6(N2Se)];ZINC;4,5,9,10,14,15-hexapropyl-21-selena-2,7,12,17,24,25,26,27-octaza-20,22-diazanidahexacyclo[16.5.1.13,6.18,11.113,16.019,23]heptacosa-1(24),2,4,6(27),7,9,11(26),12,14,16(25),17,19(23)-dodecaene
[7,8,12,13,17,18-hexapropyl-[1,2,5]selenadiazolo[3,4-q]porphyrazinato]zinc(II)化学式
CAS
888014-95-7
化学式
C34H42N10SeZn
mdl
——
分子量
735.124
InChiKey
CFUPDGCKFGQEET-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):
    8.44
  • 重原子数:
    46
  • 可旋转键数:
    12
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    101
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    [7,8,12,13,17,18-hexapropyl-[1,2,5]selenadiazolo[3,4-q]porphyrazinato]zinc(II) 在 H2S 、 C5H5N 作用下, 以 吡啶 为溶剂, 生成 N,O-copper(II)-[7,8,12,13,17,18-hexapropyl-2-(5-tert-butyl-2-oxybenzylideneamino)-3-(quinoline-2-carboxamido)porphyrazinato]zinc(II)
    参考文献:
    名称:
    Porphyrazines as Molecular Scaffolds:  Flexible Syntheses of Novel Multimetallic Complexes
    摘要:
    Reductive deselenation of selenodiazole-fused porphyrazines, followed by acylation of the resultant labile porphyrazinediamines, was used to prepare macrocycles bearing two Collins ligands, two oxamido residues, or two quinoline-2-carboxamido units. Peripheral coordination of copper(II) to the di-(quinoline-2-carboxamido)porphyrazine gave a metal-linked face-to-face porphyrazine dimer array. Sequential derivatization of the two amino groups in the porphyrazinediamines was used to prepare mixed peripheral ligand systems including a dimetallic picolinamido-Schiff base porphyrazine. Such systems exhibit strong metal-metal spin coupling and are anticipated to be of value in the synthesis of novel electronic and magnetic materials.
    DOI:
    10.1021/ic060176n
  • 作为产物:
    描述:
    7,8,12,13,17,18-hexapropyl-[1,2,5]selenadiazolo[3,4-q]porphyrazine 、 zinc diacetate 在 (CH3)2NCHO 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以83%的产率得到[7,8,12,13,17,18-hexapropyl-[1,2,5]selenadiazolo[3,4-q]porphyrazinato]zinc(II)
    参考文献:
    名称:
    Porphyrazines as Molecular Scaffolds:  Flexible Syntheses of Novel Multimetallic Complexes
    摘要:
    Reductive deselenation of selenodiazole-fused porphyrazines, followed by acylation of the resultant labile porphyrazinediamines, was used to prepare macrocycles bearing two Collins ligands, two oxamido residues, or two quinoline-2-carboxamido units. Peripheral coordination of copper(II) to the di-(quinoline-2-carboxamido)porphyrazine gave a metal-linked face-to-face porphyrazine dimer array. Sequential derivatization of the two amino groups in the porphyrazinediamines was used to prepare mixed peripheral ligand systems including a dimetallic picolinamido-Schiff base porphyrazine. Such systems exhibit strong metal-metal spin coupling and are anticipated to be of value in the synthesis of novel electronic and magnetic materials.
    DOI:
    10.1021/ic060176n
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文献信息

  • Porphyrazines as Molecular Scaffolds:  Flexible Syntheses of Novel Multimetallic Complexes
    作者:Tomasz Goslinski、Chang Zhong、Matthew J. Fuchter、Charlotte L. Stern、Andrew J. P. White、Anthony G. M. Barrett、Brian M. Hoffman
    DOI:10.1021/ic060176n
    日期:2006.5.1
    Reductive deselenation of selenodiazole-fused porphyrazines, followed by acylation of the resultant labile porphyrazinediamines, was used to prepare macrocycles bearing two Collins ligands, two oxamido residues, or two quinoline-2-carboxamido units. Peripheral coordination of copper(II) to the di-(quinoline-2-carboxamido)porphyrazine gave a metal-linked face-to-face porphyrazine dimer array. Sequential derivatization of the two amino groups in the porphyrazinediamines was used to prepare mixed peripheral ligand systems including a dimetallic picolinamido-Schiff base porphyrazine. Such systems exhibit strong metal-metal spin coupling and are anticipated to be of value in the synthesis of novel electronic and magnetic materials.
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