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| 142340-19-0

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
142340-19-0
化学式
C45H45NO3P2PtS
mdl
——
分子量
936.951
InChiKey
PUQKVYQHOVAXJX-FWCFMKQDSA-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):
    9.06
  • 重原子数:
    53.0
  • 可旋转键数:
    13.0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.16
  • 拓扑面积:
    46.61
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

反应信息

  • 作为产物:
    描述:
    苄基二苯膦N-乙酰-DL-蛋氨酸dichloro( 1,5-cyclooctadiene)platinum(ll) 在 Ag2O 作用下, 以 二氯甲烷 为溶剂, 以95%的产率得到
    参考文献:
    名称:
    Synthesis and reactivity of N-acetylamino acidate(2–) and related complexes of platinum(II)
    摘要:
    Treatment of the complexes [PtCl2L2](L = P-donor ligand) with the N-acetyl derivatives of the amino acids glycine, DL-alanine, DL-methionine or L-phenylalanine in the presence of an excess of silver(I) oxide in refluxing dichloromethane affords [Pt{N(COMe)CHRC(O)O}L2] (R = H, Me, CH2CH2SMe or CH2Ph) respectively, and with L-proline the complexes [Pt{NCH2CH2CH2CHC(O)O}L2] are produced, Similar treatment with the N-formyl or N-trifluoroacetyl derivatives of glycine gave the complexes [Pt{N(R)CH2C(O)}2] (R = CHO or COCF3) respectively. An X-ray crystal structure study on the N-acetylglycinato(2-)-N,O complex [Pt{N(COMe)CH2C(O)O}(dppe)] (dppe = Ph2PCH2CH2PPh2) indicated the presence of an almost planar five-membered ring with substantial electron delocalisation within the carboxylate and amide functionalities. Treatment of the complexes [PtCl2L2] with DL-mandelic (alpha-hydroxybenzeneacetic) acid, 2-acetamidophenol, pyrrole-2-carboxylic acid, mercaptoacetic acid or oxamic acid in the presence of an excess of Ag2O in refluxing dichloromethane afforded the complexes [Pt{OC(H)PhC(O)O}L2], [Pt{o-N(COMe)C6H4O}L2], [Pt{NCH = C(H)CH = CC(O)O}L2], [Pt{SCH2C(O)O}L2], [Pt{N(H)C(O)C(O)O}L2] respectively. The cycloocta-1,5-diene (cod) ligand of [Pt{N(COMe)CH2C(O)O}(cod)] and [Pt{N(COMe)CH(CH2Ph)C(O)O}(cod)] is readily displaced by tertiary phosphines. One mole equivalent of Bu(t)NC stereospecifically displaces the PPh3 ligand opposite oxygen in the complex [Pt{N(COMe)CH(CH2Ph)C(O)P}(PPh3)2]. Treatment of [Pt{N(COMe)CH2C(O)O}(PPh3)2] in refluxing ethanol with an excess of either diphenylacetylene or PPh3 leads to the formation of [Pt(PhC = CPh)(PPh3)2] or [Pt(PPh3)4] respectively, in good yield. Treatment of the same metal complex in ethanol at room temperature with either SO2 or CO led to the formation of the bis(ethanesulfonate) or bis(ethoxycarbonyl) complexes respectively. The complex [Pt{NCHCH2CH2CHC(O)O}(PPh3)2] induces the polymerisation of hexaflurobut-2-yne.
    DOI:
    10.1039/dt9920001165
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