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| 1549703-11-8

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1549703-11-8
化学式
C27H24N3ORhS2
mdl
——
分子量
573.545
InChiKey
YSPVMERCDABGSI-UHFFFAOYSA-M
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

  • 作为产物:
    描述:
    morpholine-4-carbodithioic acid 、 [Rh(2-C6H4py)2Cl]2*1/4CH2Cl2二甲基亚砜乙腈 为溶剂, 反应 12.0h, 以80%的产率得到
    参考文献:
    名称:
    Cyclometalated rhodium(III) complexes bearing dithiocarbamate derivative: Synthesis, characterization, interaction with DNA and biological study
    摘要:
    Reaction of three different dithiocarbamates (4-MePipzcdtH, (LH)-H-1; MorphcdtH, (LH)-H-2 and 4-BzPipercdtH, (LH)-H-3) with [Rh(2-C(6)H(4)py)(2)Cl](2)center dot 1/4CH(2)Cl(2) afforded a class of rhodium(III) complexes of the type [Rh-III(2-C(6)H(4)py)(2)(L)]. The complexes were fully characterized by several spectroscopic tools along with a detailed structural characterization of [Rh(2-C(6)H(4)py)2(L-1)] (1) by single crystal X-ray diffraction. Structural analysis of 1 showed a distorted octahedron in which both of the 2-phenylpyridyl nitrogens are in axial positions, trans to one another and the sulfur atoms are opposite to the phenyl rings. Electrochemical analysis by cyclic voltammetry reveals irreversible redox behavior of the rhodium centre in 1,2 and 3. Their DNA binding ability have been also evaluated from the absorption spectral study as well as fluorescence quenching properties, suggesting the intercalative interaction of the complexes with CT-DNA due to the stacking between the aromatic chromophore and the base pairs of DNA. Antibacterial activity of complexes has also been studied by agar disc diffusion method against some species of pathogenic bacteria (Escherichia coli, Vibrio cholerae, Streptococcus pneumonia and Bacillus cereus). (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2013.11.028
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