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Pt(N-butyl-pyridine-2-carbaldimine)(2-((4,5-ethylenedithio)-1,3-dithiol-2-ylidene)-1,3-dithiol-4,5-dithionate(2-)) | 335080-09-6

中文名称
——
中文别名
——
英文名称
Pt(N-butyl-pyridine-2-carbaldimine)(2-((4,5-ethylenedithio)-1,3-dithiol-2-ylidene)-1,3-dithiol-4,5-dithionate(2-))
英文别名
Pt(Bu-pya)(C8H4S8)
Pt(N-butyl-pyridine-2-carbaldimine)(2-((4,5-ethylenedithio)-1,3-dithiol-2-ylidene)-1,3-dithiol-4,5-dithionate(2-))化学式
CAS
335080-09-6
化学式
C18H18N2PtS8
mdl
——
分子量
713.962
InChiKey
FZWUTAVYIRWDJE-OTBYXNOXSA-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:
    Pt(N-butyl-pyridine-2-carbaldimine)(2-((4,5-ethylenedithio)-1,3-dithiol-2-ylidene)-1,3-dithiol-4,5-dithionate(2-))氯仿N,N-二甲基甲酰胺 为溶剂, 以33%的产率得到[Pt(N-butyl-pyridine-2-carbaldimine)(2-((4,5-ethylenedithio)-1,3-dithiol-2-ylidene)-1,3-dithiol-4,5-dithionate(2-))](I3)
    参考文献:
    名称:
    Preparation of Pt(II) and Pd(II) complexes coordinated with both a diimine ligand and a sulfur-rich dithiolate ligand and electrical conductivities of their oxidized species and X-ray crystal structure of Pd(N-butyl-pyridine-2-carbaldimine)(C3S5)
    摘要:
    Pt(L)(C8H4S8) [L = 2,2 ' -bipyridine (bpy) and N-butyl-pyridine-2-carbaldimine (Bu-pya): C8H4S82- = 2-{(4,5-ethylenedithio)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithionate(2-)]. Pd(Bu-pya)(C8H4S8), and Pd(Bu-pya)(C3S8) [C10-C6S82- = 2-{bis(dodecylthio)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithiolate(2-)]. Pd(Bu-pya)(C8H4S8), and Pd(Bu-pya)(C3S8) [C3S82- = 4,5-disulfanyl-1,3-dithiol-2-thionate(2-)] were prepared. They showed intense electronic absorption bands due to an intramolecular mixed ligand-to-ligand charge transfer transition which is sensitive to a solvent. They exhibit oxidation potentials of -0.18 and +0.35 V (versus Ag/Ag-) with oxidation of the dithiolate ligand. They were oxidized by iodine or TCNQ (7,7,8,8-tetracyano-p-quinodimethane) to afford [Pt(L)(C8H4S8)](I-3)(y)(x = 0.9-1.0). [Pt(L)(C8H4S8)](TCNQ)(x) (y = 0.6-0.8) (L = bpy), Bu-pya and C10-C6S8) and [Pd(Bu-pya)(C8H4S8)I-.(5.1) and [Pd(Bu-pya)(C8H4S8)](TCNQ)(0.4). The [Pt(L)(C8H4S8)]-oxidized complexes behave as electrical conductors with conductivities of 1.4 x 10(-5)-10(-3) S cm(-1) measured for compacted pellets at room temperature, while the [Pd(Bu-pya)(C8H4S8)]-oxidized species exhibit conductivities of (1.4-3.2) x 10(-3) S cm(-1). The X-ray crystal structure of Pd(Bu-pya)(C3S8) revealed a one-dimensional array of the molecules constructed with some sulfur-sulfur non-bonded contacts. (C) 2000 Elesevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(00)00274-7
  • 作为产物:
    描述:
    dichloro(N-butyl-pyridine-2-carbaldimine)platinum(II)4,5-bis(cyanoethylthio)-1,3-dithiole-2-[(4,5-ethylenedithio)-1,3-dithiole-2-ylidene] 在 Na 作用下, 以 乙醇 为溶剂, 以20%的产率得到Pt(N-butyl-pyridine-2-carbaldimine)(2-((4,5-ethylenedithio)-1,3-dithiol-2-ylidene)-1,3-dithiol-4,5-dithionate(2-))
    参考文献:
    名称:
    Preparation of Pt(II) and Pd(II) complexes coordinated with both a diimine ligand and a sulfur-rich dithiolate ligand and electrical conductivities of their oxidized species and X-ray crystal structure of Pd(N-butyl-pyridine-2-carbaldimine)(C3S5)
    摘要:
    Pt(L)(C8H4S8) [L = 2,2 ' -bipyridine (bpy) and N-butyl-pyridine-2-carbaldimine (Bu-pya): C8H4S82- = 2-{(4,5-ethylenedithio)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithionate(2-)]. Pd(Bu-pya)(C8H4S8), and Pd(Bu-pya)(C3S8) [C10-C6S82- = 2-{bis(dodecylthio)-1,3-dithiol-2-ylidene}-1,3-dithiol-4,5-dithiolate(2-)]. Pd(Bu-pya)(C8H4S8), and Pd(Bu-pya)(C3S8) [C3S82- = 4,5-disulfanyl-1,3-dithiol-2-thionate(2-)] were prepared. They showed intense electronic absorption bands due to an intramolecular mixed ligand-to-ligand charge transfer transition which is sensitive to a solvent. They exhibit oxidation potentials of -0.18 and +0.35 V (versus Ag/Ag-) with oxidation of the dithiolate ligand. They were oxidized by iodine or TCNQ (7,7,8,8-tetracyano-p-quinodimethane) to afford [Pt(L)(C8H4S8)](I-3)(y)(x = 0.9-1.0). [Pt(L)(C8H4S8)](TCNQ)(x) (y = 0.6-0.8) (L = bpy), Bu-pya and C10-C6S8) and [Pd(Bu-pya)(C8H4S8)I-.(5.1) and [Pd(Bu-pya)(C8H4S8)](TCNQ)(0.4). The [Pt(L)(C8H4S8)]-oxidized complexes behave as electrical conductors with conductivities of 1.4 x 10(-5)-10(-3) S cm(-1) measured for compacted pellets at room temperature, while the [Pd(Bu-pya)(C8H4S8)]-oxidized species exhibit conductivities of (1.4-3.2) x 10(-3) S cm(-1). The X-ray crystal structure of Pd(Bu-pya)(C3S8) revealed a one-dimensional array of the molecules constructed with some sulfur-sulfur non-bonded contacts. (C) 2000 Elesevier Science B.V. All rights reserved.
    DOI:
    10.1016/s0020-1693(00)00274-7
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