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[Sn2Cl7(1,2-bis(1H-benzimidazol-2-yl)-1,2-ethanediol(-1H))] | 958870-65-0

中文名称
——
中文别名
——
英文名称
[Sn2Cl7(1,2-bis(1H-benzimidazol-2-yl)-1,2-ethanediol(-1H))]
英文别名
——
[Sn2Cl7(1,2-bis(1H-benzimidazol-2-yl)-1,2-ethanediol(-1H))]化学式
CAS
958870-65-0
化学式
C16H13Cl7N4O2Sn2
mdl
——
分子量
778.896
InChiKey
PYZOQVIOPZGBFS-FLYCNLMGSA-G
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:
    [Sn2Cl7(1,2-bis(1H-benzimidazol-2-yl)-1,2-ethanediol(-1H))] 、 1,8-dihydro-1,3,6,8,10,13-hexaazacyclotetradecane-copper(II) perchlorate 在 sodium hydroxide 作用下, 以 甲醇乙腈 为溶剂, 以60%的产率得到
    参考文献:
    名称:
    Stannoxane capping derived from chiral tridentate NNO donor ligand for nickel and copper macrocycles: Comparative binding studies of stannoxane moiety and its modulated copper complex with CTDNA
    摘要:
    Novel stannoxane type dinuclear tin complex C16H13N4O2Sn2Cl7 (1) and its modulated macrocyclic complexes [C24H36N10O3Sn2CUCl7] ClO4 (2) and [C24H34N10O2Sn2NiCl7) ClO4 (3) were synthesized and characterized by elemental analysis and various spectroscopic techniques (1R, H-1, C-13, Sn-119 NMR, ESI-MS, EPR and UV-Vis). Sn-119 NMR shows the presence of two tin metal centers in different environment. The proposed pseudo-octahedral geometry of copper in complex 2 and square pyramidal geometry of nickel in complex 3 were established by the analysis of spectroscopic data. Absorption and fluorescence spectral studies and viscosity measurements have been carried out to assess the comparative binding of dinuclear stannoxane complex 1 and its modulated copper complex 2 with calf thymus DNA. The intrinsic binding constants K-b of the complex 1 and 2 were determined as 4.4 x 10(4) M-1 and 7.5 x 10(4) M-1, respectively. Cyclic voltammetric studies have also been employed to ascertain the binding of complex 2 with CTDNA. The results suggest that the complex 2 binds to CTDNA twice in the order of magnitude compared to complex 1. Interaction studies of complex 2 with guanosine 5'-monophosphate further confirm the binding via N-7 position of guanine and phosphate moiety. (c) 2007 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2007.07.044
  • 作为产物:
    描述:
    1,2-双(1H-苯并咪唑-2-基)乙烷-1,2-二醇四氯化锡甲醇四氯化碳 为溶剂, 以62%的产率得到[Sn2Cl7(1,2-bis(1H-benzimidazol-2-yl)-1,2-ethanediol(-1H))]
    参考文献:
    名称:
    Stannoxane capping derived from chiral tridentate NNO donor ligand for nickel and copper macrocycles: Comparative binding studies of stannoxane moiety and its modulated copper complex with CTDNA
    摘要:
    Novel stannoxane type dinuclear tin complex C16H13N4O2Sn2Cl7 (1) and its modulated macrocyclic complexes [C24H36N10O3Sn2CUCl7] ClO4 (2) and [C24H34N10O2Sn2NiCl7) ClO4 (3) were synthesized and characterized by elemental analysis and various spectroscopic techniques (1R, H-1, C-13, Sn-119 NMR, ESI-MS, EPR and UV-Vis). Sn-119 NMR shows the presence of two tin metal centers in different environment. The proposed pseudo-octahedral geometry of copper in complex 2 and square pyramidal geometry of nickel in complex 3 were established by the analysis of spectroscopic data. Absorption and fluorescence spectral studies and viscosity measurements have been carried out to assess the comparative binding of dinuclear stannoxane complex 1 and its modulated copper complex 2 with calf thymus DNA. The intrinsic binding constants K-b of the complex 1 and 2 were determined as 4.4 x 10(4) M-1 and 7.5 x 10(4) M-1, respectively. Cyclic voltammetric studies have also been employed to ascertain the binding of complex 2 with CTDNA. The results suggest that the complex 2 binds to CTDNA twice in the order of magnitude compared to complex 1. Interaction studies of complex 2 with guanosine 5'-monophosphate further confirm the binding via N-7 position of guanine and phosphate moiety. (c) 2007 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2007.07.044
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