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Ru(6-phenyl-2,4-di(2-pyridyl)-s-triazine)Cl3 | 873216-50-3

中文名称
——
中文别名
——
英文名称
Ru(6-phenyl-2,4-di(2-pyridyl)-s-triazine)Cl3
英文别名
——
Ru(6-phenyl-2,4-di(2-pyridyl)-s-triazine)Cl3化学式
CAS
873216-50-3
化学式
C19H13Cl3N5Ru
mdl
——
分子量
518.775
InChiKey
RAORYHHEVJUBPH-UHFFFAOYSA-K
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

反应信息

  • 作为反应物:
    描述:
    Ru(6-phenyl-2,4-di(2-pyridyl)-s-triazine)Cl34-([2,2':6',2''-三联吡啶]-4'-基)苯甲酸 在 AgNO3 作用下, 以 乙醇 为溶剂, 以41%的产率得到[(4'-(p-carboxyphenyl)-2,2':6',2''-terpyridine)Ru(6-phenyl-2,4-di(2-pyridyl)-s-triazine)](PF6)2
    参考文献:
    名称:
    Self-Assembled Light-Harvesting Systems:  Ru(II) Complexes Assembled about Rh−Rh Cores
    摘要:
    Ru(II) polypyridine species have been assembled about dirhodium(II, II) tetracarboxylate cores. The complexes prepared have general formulas [{(terpy)Ru(La)}(n){Rh-2(CH3COO)(4-n)(CH3CN)(2)}](2n+) (a-type compounds: terpy = 2,2':6',2' '-terpyridine; La = 4'-(p-carboxyphenyl)-2,2':6',2' '-terpyridine; n = 1, 1a; n = 2, cis-2a and trans-2a-cis and trans refer to the arrangement of the Ru(II) species around the dirhodium core; n = 3, 3a), [{(Lb)Ru(La)}(n){Rh-2(CH3COO)(4-n)(CH3CN)(2)}](2n+) (b-type compounds: Lb = 6-phenyl-2,4-di(2-pyridyl)-s-triazine; n = 1, 1b; n = 2, an inseparable mixture of cis-2b and trans-2b; n = 3, 3b; n = 4, 4b), and [{(terpy)Ru(Lc)}{Rh-2(CH3COO)(3)(CH3CN)(2)}](2+) (1c; Lc = 6-(p-carboxyphenyl)-2,4-di(2-pyridyl)-s-triazine). As model species, also the mononuclear [(terpy)Ru(La)](2+) (5a), [(La)Ru(Lb)](2+) (5b), and [(terpy)Ru(Lc)](2+) (5c) have been prepared. All of the complexes have been characterized by several techniques, including NMR and mass spectra, and the stability of the various species is discussed. The absorption spectra of all of the compounds are dominated by the Ru(II) polypyridine moieties, showing intense ligand-centered (LC) bands in the UV region and intense metal-to-ligand charge-transfer (MLCT) bands in the visible. The compounds exhibit several metal-centered oxidation and ligand-centered reduction processes, which have been assigned to specific subunits. Both absorption and redox data indicate a supramolecular nature of the assembled systems. Efficient energy transfer from the MLCT triplet state of the Ru-based components to the lowest-energy excited state of the dirhodium core takes place for the a-type compounds at 298 K in acetonitrile solution, whereas such a process is inefficient for the b-type and c-type species, which exhibit the typical MLCT emission. At 77 K in butyronitrile matrix, Ru-to-Rh-2 energy transfer is partly efficient for both the a-type and the b-type compounds and is inefficient for 1c. The reasons for such behavior are discussed by taking into account arguments concerning the driving force and reorganization energy of the complexes.
    DOI:
    10.1021/ja072153t
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