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Ru(2,6-(4-CH3OC6H4NCO)2C5H3N)(2,2',2''-terpyridine) | 1007838-78-9

中文名称
——
中文别名
——
英文名称
Ru(2,6-(4-CH3OC6H4NCO)2C5H3N)(2,2',2''-terpyridine)
英文别名
Ru(2,6-(4-CH3OC6H4NCO)2C5H3N)(trpy)
Ru(2,6-(4-CH3OC6H4NCO)2C5H3N)(2,2',2''-terpyridine)化学式
CAS
1007838-78-9
化学式
C36H28N6O4Ru
mdl
——
分子量
709.726
InChiKey
OROXVZXFJUVARD-UHFFFAOYSA-L
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:
    Ru(2,6-(4-CH3OC6H4NCO)2C5H3N)(2,2',2''-terpyridine)四丁基高氯酸铵二氯甲烷乙腈 为溶剂, 以99%的产率得到[Ru(2,6-(4-CH3OC6H4NCO)2C5H3N)(2,2',2''-terpyridine)]ClO4
    参考文献:
    名称:
    N,N′-Bis(aryl)pyridine-2,6-dicarboxamide complexes of ruthenium: Synthesis, structure and redox properties
    摘要:
    Reaction of five N,N'-bis(aryl)pyridine-2,6-dicarboxamides (H2L-R, where H-2 denotes the two acidic protons and R (R = OCH3, CH3, H, Cl and NO2) the para substituent in the aryl fragment) with [Ru(trpy)Cl-3](trpy = 2,2',2"-terpyridine) in refluxing ethanol in the presence of a base (NEW affords a group of complexes of the type [Ru-II(trpy)(L-R)], each of which contains an amide ligand coordinated to the metal center as a dianionic tridentate N,N,N-donor along with a terpyridine ligand. Structure of the [Ru-II(trpy)(L-Cl)] complex has been determined by X-ray crystallography. All the Ru(II) complexes are diamagnetic, and show characteristic H-1 NMR signals and intense MLCT transitions in the visible region. Cyclic voltammetry on the [Ru-II(trpy)(L-R)] complexes shows a Ru(II)-Ru(III) oxidation within 0.16-0.33 V versus SCE. An oxidation of the coordinated amide ligand is also observed within 0.94-1.33 V versus SCE and a reduction of coordinated terpyridine ligand within -1.10 to -1.15 V versus SCE. Constant potential coulometric oxidation of the [Ru-II(trpy)(L-R)] complexes produces the corresponding [Ru-II(trpy)(L-R)](+) complexes, which have been isolated as the perchlorate salts. Structure of the [Ru-III(trpy)(L-CH3)ClO4 complex has been determined by X-ray crystallography. All the Ru(Ill) complexes are one-electron paramagnetic, and show anisotropic ESR spectra at 77 K and intense LMCT transitions in the visible region. A weak ligand-field band has also been shown by all the [Ru-III(trpy)(L-R)]ClO4 complexes near 1600 nm. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2007.08.042
  • 作为产物:
    参考文献:
    名称:
    N,N′-Bis(aryl)pyridine-2,6-dicarboxamide complexes of ruthenium: Synthesis, structure and redox properties
    摘要:
    Reaction of five N,N'-bis(aryl)pyridine-2,6-dicarboxamides (H2L-R, where H-2 denotes the two acidic protons and R (R = OCH3, CH3, H, Cl and NO2) the para substituent in the aryl fragment) with [Ru(trpy)Cl-3](trpy = 2,2',2"-terpyridine) in refluxing ethanol in the presence of a base (NEW affords a group of complexes of the type [Ru-II(trpy)(L-R)], each of which contains an amide ligand coordinated to the metal center as a dianionic tridentate N,N,N-donor along with a terpyridine ligand. Structure of the [Ru-II(trpy)(L-Cl)] complex has been determined by X-ray crystallography. All the Ru(II) complexes are diamagnetic, and show characteristic H-1 NMR signals and intense MLCT transitions in the visible region. Cyclic voltammetry on the [Ru-II(trpy)(L-R)] complexes shows a Ru(II)-Ru(III) oxidation within 0.16-0.33 V versus SCE. An oxidation of the coordinated amide ligand is also observed within 0.94-1.33 V versus SCE and a reduction of coordinated terpyridine ligand within -1.10 to -1.15 V versus SCE. Constant potential coulometric oxidation of the [Ru-II(trpy)(L-R)] complexes produces the corresponding [Ru-II(trpy)(L-R)](+) complexes, which have been isolated as the perchlorate salts. Structure of the [Ru-III(trpy)(L-CH3)ClO4 complex has been determined by X-ray crystallography. All the Ru(Ill) complexes are one-electron paramagnetic, and show anisotropic ESR spectra at 77 K and intense LMCT transitions in the visible region. A weak ligand-field band has also been shown by all the [Ru-III(trpy)(L-R)]ClO4 complexes near 1600 nm. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2007.08.042
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