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chlorido(2,6-bis[(1,3-di-tert-butylimidazolin-2-imino)methyl]pyridine)platinum(II) perchlorate | 1383707-18-3

中文名称
——
中文别名
——
英文名称
chlorido(2,6-bis[(1,3-di-tert-butylimidazolin-2-imino)methyl]pyridine)platinum(II) perchlorate
英文别名
——
chlorido(2,6-bis[(1,3-di-tert-butylimidazolin-2-imino)methyl]pyridine)platinum(II) perchlorate化学式
CAS
1383707-18-3
化学式
C29H47ClN7Pt*ClO4
mdl
——
分子量
823.723
InChiKey
WQSGPNVPGSEQQX-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:
    氢碘酸chlorido(2,6-bis[(1,3-di-tert-butylimidazolin-2-imino)methyl]pyridine)platinum(II) perchlorate 在 NaCl 、 NaClO4 作用下, 以 为溶剂, 生成 (2,6-bis[(1,3-di-tert-butylimidazolin-2-imino)methyl]pyridine)(iodido)platinum(II)
    参考文献:
    名称:
    Ligand substitution reactions of some sterically hindered Pt(II) complexes. The crystal structures of [TLBuH2](ClO4)2·0.5H2O
    摘要:
    Substitution reactions of the complexes [(TLtBu)PtCl](+) and [Pt(tpdm)Cl](+), where TLtBu = 2,6-bis[(1,3-ditert-butylimidazolin-2-imino)methyl]pyridine and tpdm = terpyridinedimethane, with nucleophiles: thiourea, I-, Br-, NO2-, pyridine and dimethyl-sulfoxide (DMSO) were studied in 0.1 M NaClO4 aqueous solution in the presence of 10 mM NaCl. The reactions were carried out at three different temperatures (288, 298 and 308 K) using variable-temperature UV-VIS spectrophotometer. The substitutions were followed under the pseudo-first-order conditions with a large excess of nucleophiles. The slightly higher reactivity of complex with tpdm ligand can be attributed to the influence of the bulkiness of tertbutyl-groups from [(TLtBu)PtCl](+) complex. The order of reactivity of studied ligands is: thiourea > I- > Br- > NO2- > pyridine > DMSO. The negative values reported for entropy of activation confirmed the associative substitution mode. These results are discussed in order to find the connection between structure and reactivity of the complexes with tridentate sterically hindered ligands. The crystal structure of [(TLH2)-H-tBU](ClO4)(2)center dot 0.5H(2)O was determined by X-ray diffraction. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2012.04.024
  • 作为产物:
    描述:
    2,6-bis[(1,3-di-tert-butylimidazolin-2-imino)methyl]pyridine高氯酸dichloro( 1,5-cyclooctadiene)platinum(ll) 、 sodium perchlorate 以 为溶剂, 以72%的产率得到chlorido(2,6-bis[(1,3-di-tert-butylimidazolin-2-imino)methyl]pyridine)platinum(II) perchlorate
    参考文献:
    名称:
    Ligand substitution reactions of some sterically hindered Pt(II) complexes. The crystal structures of [TLBuH2](ClO4)2·0.5H2O
    摘要:
    Substitution reactions of the complexes [(TLtBu)PtCl](+) and [Pt(tpdm)Cl](+), where TLtBu = 2,6-bis[(1,3-ditert-butylimidazolin-2-imino)methyl]pyridine and tpdm = terpyridinedimethane, with nucleophiles: thiourea, I-, Br-, NO2-, pyridine and dimethyl-sulfoxide (DMSO) were studied in 0.1 M NaClO4 aqueous solution in the presence of 10 mM NaCl. The reactions were carried out at three different temperatures (288, 298 and 308 K) using variable-temperature UV-VIS spectrophotometer. The substitutions were followed under the pseudo-first-order conditions with a large excess of nucleophiles. The slightly higher reactivity of complex with tpdm ligand can be attributed to the influence of the bulkiness of tertbutyl-groups from [(TLtBu)PtCl](+) complex. The order of reactivity of studied ligands is: thiourea > I- > Br- > NO2- > pyridine > DMSO. The negative values reported for entropy of activation confirmed the associative substitution mode. These results are discussed in order to find the connection between structure and reactivity of the complexes with tridentate sterically hindered ligands. The crystal structure of [(TLH2)-H-tBU](ClO4)(2)center dot 0.5H(2)O was determined by X-ray diffraction. (c) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2012.04.024
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