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trans-[(CH3NH2)2Pt(1,3-dimethyluracilate-C5)(H2O)](ClO4) | 173776-53-9

中文名称
——
中文别名
——
英文名称
trans-[(CH3NH2)2Pt(1,3-dimethyluracilate-C5)(H2O)](ClO4)
英文别名
——
trans-[(CH3NH2)2Pt(1,3-dimethyluracilate-C5)(H2O)](ClO4)化学式
CAS
173776-53-9
化学式
C8H19N4O3Pt*ClO4
mdl
——
分子量
513.794
InChiKey
WAICNIIKVANHQT-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

  • 作为反应物:
    参考文献:
    名称:
    The Uracil C(5) Position as a Metal Binding Site:  Solution and X-ray Crystal Structure Studies of PtII and HgII Compounds
    摘要:
    1,3-Dimethyluracil (1,3-DimeU) reacts with trans-[(CH3NH2)(2)Pt(H2O)(2)](+) to give trans-[(CH3NH2)(2)Pt(1,3-DimeU-C-5)(H2O)]X (X = NO3-, 1a, ClO4-, 1b) and subsequently with NaCl to give trans-(CH3NH2)(2)Pt(1,3-DimeU-C5)Cl (2) or with NH3 to yield trans-[(CH3NH2)(2)Pt(1,3-DimeU-C5)(NH3)]Cl (3). In a similar way, (dien)Pt-II forms [dienPt(1,3-DimeU-C5)](+) (4). Reactions leading to formation of 1 and 4 are slow, taking days. In contrast, Hg(CH3COO)(2) reacts fast with 1,3-DimeU to give (1,3-DimeU-C5)Hg(CH3COO) (5). Both 1-methyluracil(1-lMeUH) and uridine (urdH) react with (dien)Pt-II initially at N(3) and subsequently with either (dien)Pt-II or Hg(CH3COO)(2) also at C(5) to give the diplatinated species 7 and 9 or the mixed PtHg complex 8. C(5) binding of either Pt-II or Hg-II is evident from coupling of uracil-H(6) with either Pt-195 or Hg-199 nuclei and (3)J values of 47-74 Hz (for Pt compounds) and 185-197 Hz (for Hg compounds). J values of Pt compounds are influenced both by the ligands trans to the uracil C(5) position and by the number of metal entities bound to a uracil ring. Both 2 and 5 were X-ray structurally characterized. 2: monoclinic system, space group P2(1)/c, a (6) Angstrom, c = 25.655 (10) Angstrom, beta = 145.55(3)degrees, V = 2621.9(28) Angstrom(3), Z = 4. 5: monoclinic system, space group P2(1)/c, a = 4.905(2) Angstrom, b = 18.451(6) Angstrom, c = 11.801(5) Angstrom, beta = 94.47(3)degrees, V = 1064.77(72) Angstrom(3), Z = 4.
    DOI:
    10.1021/ic950842c
  • 作为产物:
    描述:
    1,3-二甲基脲嘧啶 、 [trans-Pt(OH2)2(NH2CH3)2](ClO4)2 为溶剂, 生成 trans-[(CH3NH2)2Pt(1,3-dimethyluracilate-C5)(H2O)](ClO4)
    参考文献:
    名称:
    The Uracil C(5) Position as a Metal Binding Site:  Solution and X-ray Crystal Structure Studies of PtII and HgII Compounds
    摘要:
    1,3-Dimethyluracil (1,3-DimeU) reacts with trans-[(CH3NH2)(2)Pt(H2O)(2)](+) to give trans-[(CH3NH2)(2)Pt(1,3-DimeU-C-5)(H2O)]X (X = NO3-, 1a, ClO4-, 1b) and subsequently with NaCl to give trans-(CH3NH2)(2)Pt(1,3-DimeU-C5)Cl (2) or with NH3 to yield trans-[(CH3NH2)(2)Pt(1,3-DimeU-C5)(NH3)]Cl (3). In a similar way, (dien)Pt-II forms [dienPt(1,3-DimeU-C5)](+) (4). Reactions leading to formation of 1 and 4 are slow, taking days. In contrast, Hg(CH3COO)(2) reacts fast with 1,3-DimeU to give (1,3-DimeU-C5)Hg(CH3COO) (5). Both 1-methyluracil(1-lMeUH) and uridine (urdH) react with (dien)Pt-II initially at N(3) and subsequently with either (dien)Pt-II or Hg(CH3COO)(2) also at C(5) to give the diplatinated species 7 and 9 or the mixed PtHg complex 8. C(5) binding of either Pt-II or Hg-II is evident from coupling of uracil-H(6) with either Pt-195 or Hg-199 nuclei and (3)J values of 47-74 Hz (for Pt compounds) and 185-197 Hz (for Hg compounds). J values of Pt compounds are influenced both by the ligands trans to the uracil C(5) position and by the number of metal entities bound to a uracil ring. Both 2 and 5 were X-ray structurally characterized. 2: monoclinic system, space group P2(1)/c, a (6) Angstrom, c = 25.655 (10) Angstrom, beta = 145.55(3)degrees, V = 2621.9(28) Angstrom(3), Z = 4. 5: monoclinic system, space group P2(1)/c, a = 4.905(2) Angstrom, b = 18.451(6) Angstrom, c = 11.801(5) Angstrom, beta = 94.47(3)degrees, V = 1064.77(72) Angstrom(3), Z = 4.
    DOI:
    10.1021/ic950842c
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