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ClPd(1-hydroxy-2-(2'-ethylthiophenylazo)naphthalene(-1H)) | 1374558-35-6

中文名称
——
中文别名
——
英文名称
ClPd(1-hydroxy-2-(2'-ethylthiophenylazo)naphthalene(-1H))
英文别名
——
ClPd(1-hydroxy-2-(2'-ethylthiophenylazo)naphthalene(-1H))化学式
CAS
1374558-35-6
化学式
C18H15ClN2OPdS
mdl
——
分子量
449.269
InChiKey
QMKVRLQTUXMMHG-LLIZZRELSA-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

  • 作为产物:
    描述:
    sodium tetrachloropalladate(II)1-hydroxy-2-(2'-ethylthiophenylazo)naphthalene乙醇 为溶剂, 以82%的产率得到ClPd(1-hydroxy-2-(2'-ethylthiophenylazo)naphthalene(-1H))
    参考文献:
    名称:
    Palladium(II) complexes of terdentate azo ligands with an O,N,S donor set: Synthesis, spectroscopic characterization, X-ray structure and TD-DFT calculations
    摘要:
    The reaction of 2-hydroxy-1-(2'-alkylthiophenylazo)naphthalenes (HL1-HL5) and 1-hydroxy-2-(2'-alkylthiophenylazo)naphthalenes (HL6-HL10) with sodium tetrachloropalladate in ethanol medium at room temperature leads to the formation of a new series of complexes of the type [Pd(L)Cl]. All the palladium compounds have been isolated in their pure form and characterized by spectral and elemental analysis data. The crystal structures of [(PdLCl)-Cl-3] (3) and [(PdLCl)-Cl-6] (6) have been determined by single crystal Xray diffraction as representative cases. The crystal structures show that both complexes have distorted square-planar structures in which he palladium(II) centers are bonded to O1 of the naphtholato function, N2 of the diazene group and Si at the 2' position of the phenyl fragment. Therefore, the ligands bind palladium(II) in a tridentate monoanionic [O, N, S] fashion, which give rise to five- and six-membered chelate rings in each case. The fourth coordination site is occupied by a chloride ion. These complexes show intense absorption bands in the visible and UV region. The nature of the electronic transitions has been examined using (TD-DFT) formalism. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2012.02.021
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