摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

3-tert-butyl-5-(tert-butylsulfanylmethyl)-1H-pyrazole;dichloropalladium | 537708-95-5

中文名称
——
中文别名
——
英文名称
3-tert-butyl-5-(tert-butylsulfanylmethyl)-1H-pyrazole;dichloropalladium
英文别名
——
3-tert-butyl-5-(tert-butylsulfanylmethyl)-1H-pyrazole;dichloropalladium化学式
CAS
537708-95-5
化学式
C12H22Cl2N2PdS
mdl
——
分子量
403.712
InChiKey
IAQMLTVOOHMCJN-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

  • 作为产物:
    描述:
    双(乙腈)氯化钯(II)5-(tert-butyl)-3-(tert-butylthiomethyl)pyrazole甲醇 为溶剂, 以95%的产率得到3-tert-butyl-5-(tert-butylsulfanylmethyl)-1H-pyrazole;dichloropalladium
    参考文献:
    名称:
    Substituent Control of Hydrogen Bonding in Palladium(II)−Pyrazole Complexes
    摘要:
    Inter- and intramolecular hydrogen bonding of an N-H group in pyrazole complexes was studied using ligands with two different groups at pyrazole C-3 and C-5. At C-5, groups such as methyl, i-propyl, phenyl, or tert-butyl were present. At C-3, side chains L-CH2- and L-CH2CH2- (L = thioether or phosphine) ensured formation of chelates to a cis-dichloropalladium(II) fragment through side-chain atom L and the pyrazole nitrogen closest to the side chain. The significance of the ligands is that by placing a ligating side chain on a ring carbon (C-3), rather than on a ring nitrogen, the ring nitrogen not bound to the metal and its attached proton are available for hydrogen bonding. As desired, seven chelate complexes examined by X-ray diffraction all showed intramolecular hydrogen bonding between the pyrazole N-H and a chloride ligand in the cis position. In addition, however, intermolecular hydrogen bonding could be controlled by the substituent at C-5: complexes with either a methyl at C-5 or no substituent there showed significant intermolecular hydrogen bonding interactions, which were completely avoided by placing a tert-butyl group at C-5. The acidity of two complexes in acetonitrile solutions was estimated to be closer to that of pyridinium ion than those of imidazolium or triethylammonium ions.
    DOI:
    10.1021/ic026104n
点击查看最新优质反应信息