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cis-{Pt(dmso)(CH3CN)Cl4} | 127642-41-5

中文名称
——
中文别名
——
英文名称
cis-{Pt(dmso)(CH3CN)Cl4}
英文别名
——
cis-{Pt(dmso)(CH3CN)Cl4}化学式
CAS
127642-41-5
化学式
C4H9Cl4NOPtS
mdl
——
分子量
456.08
InChiKey
LTDLVZUWPGXAHL-UHFFFAOYSA-J
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:
    cis-{Pt(dmso)(CH3CN)Cl4} 为溶剂, 以10%的产率得到(Et4N){Pt(dmso)Cl5}*1/6NH4Cl
    参考文献:
    名称:
    Hydrolysis of organonitriles and carboxamides in platinum(IV) complexes. X-ray structure determination of the crystalline clathrate {(C2H5)}4N [Pt(NH3)Cl5]· NH4Cl
    摘要:
    DOI:
    10.1016/s0020-1693(00)80789-6
  • 作为产物:
    描述:
    参考文献:
    名称:
    Hydrolysis of organonitriles and carboxamides in platinum(IV) complexes. X-ray structure determination of the crystalline clathrate {(C2H5)}4N [Pt(NH3)Cl5]· NH4Cl
    摘要:
    DOI:
    10.1016/s0020-1693(00)80789-6
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文献信息

  • The metalla-Pinner reaction between Pt(<scp>iv</scp>)-bound nitriles and alkylated oxamic and oximic forms of hydroxamic acids
    作者:Konstantin V. Luzyanin、Vadim Yu. Kukushkin、Matti Haukka、J. J. R. Fraústo da Silva、Armando J. L. Pombeiro
    DOI:10.1039/b406600f
    日期:——
    The nitrile ligands in the platinum(IV) complexes trans-[PtCl4(RCN)2] (R = Me, Et, CH2Ph) and cis/trans-[PtCl4(MeCN)(Me2O)] are involved in a metalla-Pinner reaction with N-methylbenzohydroxamic acid (N-alkylated form of hydroxamic acid, hydroxamic form; F1), PhC(O)N(Me)OH, to achieve the imino species [PtCl4NHC(R)ON(Me)C(O)Ph}2] (1–3) and [PtCl4NHC(Me)ON(Me)C(O)Ph}(Me2O)] (7), respectively. Treatment of trans-[PtCl4(RCN)2] (R = Me, Et) and cis/trans-[PtCl4(MeCN)(Me2O)] with the O-alkylated form of a hydroxamic acid (hydroximic form), i.e. methyl 2,4,6-trimethylbenzohydroximate, 2,4,6-(Me3C6H2)C(OMe)NOH (F2A), allows the isolation of [PtCl4NHC(R)ONC(OMe)(2,4,6-Me3C6H2)}2] (5, 6) and [PtCl4NHC(Me)ONC(OMe)(2,4,6-Me3C6H2)}(Me2O)] (8), correspondingly. In accord with the latter reaction, the coupling of nitriles in trans-[PtCl4(EtCN)2] with methyl benzohydroximate, PhC(OMe)NOH (F2B), gives [PtCl4NHC(Et)ONC(OMe)Ph}2] (4). The addition proceeds faster with the hydroximicF2, rather than with the hydroxamic form F1. The complexes 1–8 were characterized by C, H, N elemental analyses, FAB+ mass-spectrometry, IR, 1H and 13C1H} NMR spectroscopies. The X-ray structure determinations have been performed for both hydroxamic and hydroximic complexes, i.e. 2 and 6, indicating that the imino ligands are mutually trans and they are in the E-configuration.
    、N、O、S、P、F、Cl、Br、I、Na、K、Li、Mg、Al、Si、Fe、Ni、Co、Mn、Cu、Zn、Y、Nb、Ta、W、Re、Os、Ir、Pt、Rh、Ru、Ag、Au、Hg、Cd、Te、Bi、Po、Sn、Ge、As、Se、Br、I、Na、K、Li、Mg、Al、Si、Fe、Ni、Co、Mn、Cu、Zn、Y、Nb、Ta、W、Re、Os、Ir、Pt、Rh、Ru、Ag、Au、Hg、Cd、Te、Bi、Po、Sn、Ge、As、Se、Br、I、Na、K、Li、Mg、Al、Si、Fe、Ni、Co、Mn、Cu、Zn、Y、Nb、Ta、W、Re、Os、Ir、Pt、Rh、Ru、Ag、Au、Hg、Cd、Te、Bi、Po、Sn、Ge、As、Se、Br、I、Na、K、Li、Mg、Al、Si、Fe、Ni、Co、Mn、Cu、Zn、Y、Nb、Ta、W、Re、Os、Ir、Pt、Rh、Ru、Ag、Au、Hg、Cd、Te、Bi、Po、Sn、Ge、As、Se、Br、I
  • Regioselective addition of bifunctional oximehydroxamic acid by the hydroxamic group to Pt(IV)-coordinated nitriles
    作者:Konstantin V. Luzyanin、Mathea S. Galanski、Vadim Yu. Kukushkin、Dmitry A. Garnovskii、Armando J.L. Pombeiro
    DOI:10.1016/j.ica.2006.12.018
    日期:2008.5
    platinum(IV) complexes trans-[PtCl4(RCN)2] (R Me, Et, CH2Ph, Ph), cis/trans-[PtCl4(MeCN)(Me2SO)] and the newly synthesized bifunctional oximehydroxamic acid, viz. N,2-dihydroxy-5-(1-hydroxyiminoethyl)benzamide, proceeds smoothly in CH2Cl2 at 40–45 °C to accomplish the new metallaligands HN C(R)ONHC( O)C6H3(2-OH)(5-C(Me) NOH) with pendant oxime functionalities due to the regioselective addition of the
    摘要(IV)配合物中反式-[PtCl4(RCN)2](R Me,Et,CH2Ph,Ph),顺式/反式-[PtCl4(MeCN)(Me2SO)]的腈RCN之间的属介导偶联以及新合成的双官能​​酸。N,2-二羟基-5-(1-羟基亚基乙基)苯甲酰胺在40-45°C的CH2Cl2中顺利进行以完成新的配体HN C(R)ONHC(O)C6H3(2-OH)(5-C( Me)(NOH)具有侧基功能,这是由于试剂通过其异羟基区域选择性加成。所得亚配体在溶液中存在异羟酸/异羟酸互变异构体平衡。分离出的化合物的结构基于元素分析(C,H,N),IR,1D 1H,13C 1H}和2D NMR相关实验,即1H,13C-COSY,1H,13C长距离COSY,1H ,15N-COSY和1H,15N远程COSY。
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