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[Ru(2,2′;6′,2″-terpyridine)(4,4′-di-tert-butyl-2,2′-bipyridine)Cl]Cl | 1346934-87-9

中文名称
——
中文别名
——
英文名称
[Ru(2,2′;6′,2″-terpyridine)(4,4′-di-tert-butyl-2,2′-bipyridine)Cl]Cl
英文别名
[Ru(terpy)(tbbpy)Cl]Cl;[Ru(2,2':6,2''-terpyridine)(4,4'-di-tert-butyl-2,2'-bipyridine)Cl]Cl
[Ru(2,2′;6′,2″-terpyridine)(4,4′-di-tert-butyl-2,2′-bipyridine)Cl]Cl化学式
CAS
1346934-87-9
化学式
C33H35ClN5Ru*Cl
mdl
——
分子量
673.65
InChiKey
ABCJTMYBLZDPAZ-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(2,2′;6′,2″-terpyridine)(4,4′-di-tert-butyl-2,2′-bipyridine)Cl]Cl甲醇丙酮 为溶剂, 反应 30.0h, 生成 [Ru(2,2′;6′,2″-terpyridine)(4,4′-di-tert-butyl-2,2′-bipyridine)(pyridine)][tetrafluoroborate]2
    参考文献:
    名称:
    Hydroxamate Anchors for Improved Photoconversion in Dye-Sensitized Solar Cells
    摘要:
    We present the first analysis of performance of hydroxamate linkers as compared to carboxylate and phosphonate groups when anchoring ruthenium-polypyriclyl dyes to TiO2 surfaces in dye-sensitized solar cells (DSSCs). The study provides fundamental insight into structure/function relationships that are critical for cell performance. Our DSSCs have been produced by using newly synthesized dye molecules and characterized by combining measurements and simulations of experimental current density-voltage (J-V) characteristic curves. We show that the choice of anchoring group has a direct effect on the overall sunlight-to-electricity conversion efficiency (eta), with hydroxamate anchors showing the best performance. Solar cells based on the pyridyl-hydroxamate complex exhibit higher efficiency since they suppress electron transfer from the photoanode to the electrolyte and have superior photoinjection characteristics. These findings suggest that hydroxamate anchoring groups should particularly valuable in DSSCs and photocatalytic applications based on molecular adsorbates covalently bound to semiconductor surfaces In contrast, analogous acetylacetonate anchors might undergo decomposition under similar conditions suggesting limited potential in future applications.
    DOI:
    10.1021/ic4010856
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