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2-(4-carboxyphenyl)-4,6-dipyrid-2-yltriazine | 951008-99-4

中文名称
——
中文别名
——
英文名称
2-(4-carboxyphenyl)-4,6-dipyrid-2-yltriazine
英文别名
6-(p-carboxyphenyl)-2,4-di(2-pyridyl)-s-triazine;4-(4,6-Dipyridin-2-yl-1,3,5-triazin-2-yl)benzoic acid;4-(4,6-dipyridin-2-yl-1,3,5-triazin-2-yl)benzoic acid
2-(4-carboxyphenyl)-4,6-dipyrid-2-yltriazine化学式
CAS
951008-99-4
化学式
C20H13N5O2
mdl
——
分子量
355.356
InChiKey
BEHZVGXVRHIVKB-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):
    2.4
  • 重原子数:
    27
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    102
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    甲醇2-(4-carboxyphenyl)-4,6-dipyrid-2-yltriazine氯化亚砜 为溶剂, 反应 2.5h, 生成
    参考文献:
    名称:
    铑-钌二聚体二聚体中的能量转移
    摘要:
    摘要提出了由三齿“吡啶类”配体Ru(II)配合物桥接的线性四羧酸四氢吡啶盐“桨轮”二聚体的合成路线。合成了三个二聚体组装体以及两个二聚体组装体。跨越两个dirhodium二聚体的双(4'-(4-羧基苯基)-吡啶)Ru(II)络合物在其X射线晶体结构中,二聚体之间显示出26 A的间隔。使用双(4'-(4-羧基)-吡啶吡啶)Ru(II)作为桥联络合物,发现没有苯基的二聚体的二聚体的电子相互作用增加。向Ru光敏剂中添加一个或两个二铑二聚体导致摩尔吸光度以累加方式增加。在排放概况中,
    DOI:
    10.1016/j.ica.2016.05.034
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文献信息

  • Self-Assembled Light-Harvesting Systems:  Ru(II) Complexes Assembled about Rh−Rh Cores
    作者:Michael W. Cooke、Garry S. Hanan、Frédérique Loiseau、Sebastiano Campagna、Masashi Watanabe、Yasutaka Tanaka
    DOI:10.1021/ja072153t
    日期:2007.8.1
    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.
  • Energy transfer in rhodium–ruthenium dimer-of-dimer assemblies
    作者:Michael W. Cooke、Marie-Pierre Santoni、Frédérique Loiseau、Bernold Hasenknopf、Garry S. Hanan
    DOI:10.1016/j.ica.2016.05.034
    日期:2017.1
    Abstract A synthetic route to linear pairs of dirhodium tetracarboxylate ‘paddlewheel’ dimers bridged by Ru(II) complexes of tridentate ‘terpyridine-like’ ligands is presented. Three dimer-of-dimer assemblies were synthesized as well as two monomer-of-dimer assemblies. A bis(4′-(4-carboxyphenyl)-terpyridine)Ru(II) complex spanning two dirhodium dimers displays a 26 A separation between the dimers in
    摘要提出了由三齿“吡啶类”配体Ru(II)配合物桥接的线性四羧酸四氢吡啶盐“桨轮”二聚体的合成路线。合成了三个二聚体组装体以及两个二聚体组装体。跨越两个dirhodium二聚体的双(4'-(4-羧基苯基)-吡啶)Ru(II)络合物在其X射线晶体结构中,二聚体之间显示出26 A的间隔。使用双(4'-(4-羧基)-吡啶吡啶)Ru(II)作为桥联络合物,发现没有苯基的二聚体的二聚体的电子相互作用增加。向Ru光敏剂中添加一个或两个二铑二聚体导致摩尔吸光度以累加方式增加。在排放概况中,
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