K[Pt(3-methylpyridine)Cl3] | 50989-05-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: K[Pt(3-methylpyridine)Cl3]
• 英文别名: K(Pt(3-picoline)Cl3)；K[Pt(3-picoline)Cl3]；K[PtCl3(3-picoline)]；K[PtCl3(3-pic)]
• CAS: 50989-05-4
• 化学式: C₆H₇Cl₃NPt*K
• 分子量: 433.666
• InChiKey: XIUYTGBSAQHNAJ-UHFFFAOYSA-K

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：

  K[Pt(3-methylpyridine)Cl3] 在 NaCl 作用下， 以 氯仿 、 水 为溶剂， 生成 trans-[PtCl2(3-picoline)(pyrazine)]
  参考文献：
  名称：

  Synthesis and characterization of the novel Pt(II) complexes of the types cis- and trans-Pt(Ypy)(pyrazine)Cl2, K2[Cl3Pt(μ-pyrazine)PtCl3] and trans, trans-(Ypy)Cl2Pt(μ-pyrazine)Pt(Ypy)Cl2 (Ypy=pyridine derivative)

  摘要：

  New types of Pt(II) mixed-ligand complexes containing a pyridine derivative (Ypy) and pyrazine (pz) were synthesized. The compounds were characterized by infrared spectroscopy and by multinuclear (H-1, C-13 and Pt-195) magnetic resonance. The complexes cis-Pt(Ypy)(pz)Cl-2 were synthesized from the reaction of K[Pt(Ypy)Cl-3] with pyrazine (1:1 proportion) in water. When the reaction was carried on in a 2:1 ratio, a mixture of compounds was obtained, which was refluxed in CH2Cl2 for several days. The final product was found to be pure and it was identified as trans, trans-Cl-2(Ypy)Pt(mu-pyrazine)Pt(Ypy)Cl-2. The cis monomers isomerize to the trans isomers in organic solvents. Different methyl derivatives of pyridine were studied in order to determine the influence of substitution in ortho position on the pyridine ligand in the complexes. In IR spectroscopy, the cis monomers showed two v(Pt-Cl) bands, while the trans monomers and dinuclear species showed only one v(Pt-Cl) band. The NMR results were interpreted in relation to the solvent effect, which seems important in these complexes. The Pt-195 NMR signals of the cis monomers were found at slightly higher. fields than those of the corresponding trans isomers. The coupling constants J(Pt-195-H-1) and J(Pt-195-C-13) are larger in the cis geometry. The delta(Pt-195) of the dinuclear species were found close to those of the trans monomers and the coupling constants are similar to those of the trans monomers, strongly suggesting a trans-trans configuration for the dinuclear compounds. The pyrazine-bridged complex K-2[Cl3Pt(mu-pz)PtCl3] was also synthesized and spectroscopically studied. The crystal structures of the compounds cis-Pt(3,5-lut)(pz)Cl-2 and trans-Pt(2,4,6-col)(pz)Cl-2 were determined by X-ray diffraction methods. (C) 2008 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.ica.2008.04.036
• 作为产物：
  描述：

  potassium tetrachloroplatinate(II) 、 3-甲基吡啶 以 not given 为溶剂， 生成 K[Pt(3-methylpyridine)Cl3]
  参考文献：
  名称：

  [Pt(L)Cl3]-(L = 吡啶衍生物)配合物的多核核磁共振谱和反式-Pt(2,6-二(羟甲基)吡啶)2Cl2•2H2O的晶体结构

  摘要：

  [Pt(L)Cl3]-（L = 吡啶衍生物）类型的配合物被合成并通过 13C 和 195Pt NMR 光谱进行研究。在 -1720 和 -1897 ppm 之间观察到 195Pt 信号。未发现质子化吡啶衍生物的 δ(Pt) 和 pKa 之间存在相关性。化学位移随吡啶配体上的取代基而变化。除了含有羟基或胺基团的配合物外，在低场观察到具有邻位取代基的化合物。后一种化合物在更高的场中观察到，接近于 Pt 未取代的吡啶化合物的信号。这些结果用溶剂效应来解释。测量了化学位移 δ(C) 和耦合常数 J(13C–195Pt)，并根据获得有关 Pt-N 键性质的信息来解释结果。检查了铂和吡啶配体之间 π 键合的可能性。吡啶环相对于铂平面的构象和...的能量

  DOI：

  10.1139/v96-241

文献信息

• Synthesis and NMR characterization of the novel mixed-ligand Pt(II) complexes cis- and trans-Pt(Ypy)(pyrimidine)Cl2 and trans,trans-Cl2(Ypy)Pt(μ-pyrimidine)Pt(Ypy)Cl2 (Ypy=pyridine derivative)
  作者：Fernande D. Rochon、Majd Fakhfakh

  DOI：10.1016/j.ica.2008.07.003

  日期：2009.4

  signals of the cis monomers were found at slightly higher fields than those of the corresponding trans isomers. The δ ( 195 Pt) of the dimers were found close to those of the trans monomers. The NMR results were interpreted in relation to the solvent effect, which seems important in these complexes. The coupling constants J ( 195 Pt– 1 H) and J ( 195 Pt– 13 C) are larger in the cis geometry. The crystal

  摘要合成了Ypy =吡啶衍生物和pm =嘧啶的顺式和反式-Pt（Ypy）（pm）Cl 2型混合配体配合物，并通过红外光谱和多核（195 Pt，1 H和13 C ）磁共振波谱学。顺式化合物是由K [Pt（Ypy）Cl 3]与嘧啶（1：1比例）在水中反应制得的，而大多数反式异构体是由顺式化合物的异构化合成的。顺式异构体不能与邻位含有两个–CH 3基团的Ypy配体分离。当以Pt∶pm比＝ 2∶1进行K [Pt（Ypy）Cl 3]与嘧啶的水反应时，形成了嘧啶桥连的双核物质。只有最稳定的反式-反式异构体才能分离出纯净的。在红外光谱中，顺式单体显示出两个ν（Pt–Cl）谱带，反式单体和二聚体仅显示一个ν（Pt–Cl）谱带。发现顺式单体的195 Pt NMR信号的场强于相应的反式异构体的场。发现二聚体的δ（195 Pt）接近反式单体的δ。解释了NMR结果与溶剂效应的关系，这在这些配合物中似乎很重要。在顺式几何中，耦合常数J（195
• Synthesis of complexes of the type <i>cis</i>-Pt(amine) (unsaturated ligand)Cl₂ and crystal structure <i>cis</i>-Pt(methylaimne) (dimethylhexynediol)Cl₂
  作者：F. D. Rochon、R. Melanson、Monique Doyon

  DOI：10.1139/v89-343

  日期：1989.12.1

  Complexes of the type cis-Pt(L)(un)Cl₂ where L = primary amine or methyl derivative of pyridine and un = cyclopentene, cyclohexene, or dimethylhexynediol, have been synthesized from the reaction of K[Pt(L)Cl₃] with the unsaturated ligand in water. The compounds were characterized and studied by ¹H NMR and IR spectroscopy. The crystal structure of cis-Pt(CH₃NH₂)((CH₃)₂C(OH)—C≡C—C(OH)(CH₃)₂)Cl₂ was determined by X-ray diffraction methods. The crystals are monoclinic, space group P2₁/c, with a = 6.544(2), b = 14.304(7), c = 15.508(7) Å, β = 109.39(2)°, and Z = 4. The coordinates and the anisotropic thermal factors were refined by full-matrix least-squares analysis to a R factor of 0.048 and wR = 0.047. The coordination around the platinum atom is square planar and the acetylenic ligand is perpendicular to the Pt plane. Keywords: platinum complexes, crystal structure, methylamine, dimethylhexynediol, synthesis.

  已经从K[Pt(L)Cl3]和不饱和配体在水中反应合成了类型为cis-Pt（L）（un）Cl2的配合物，其中L = 主要胺或吡啶的甲基衍生物，un = 环戊烯，环己烯或二甲基己炔二醇。这些化合物通过1H NMR和IR光谱进行了表征和研究。使用X射线衍射方法确定了cis-Pt（ NH2）（（CH3）2C（OH）—C≡C—C（OH）（ ）2）Cl2的晶体结构。晶体为单斜晶系，空间群P21/c，a = 6.544（2），b = 14.304（7），c = 15.508（7）Å，β = 109.39（2）°，Z = 4。通过完全矩阵最小二乘分析对坐标和各向异性热因子进行了修正，得到了R因子为0.048和wR = 0.047。铂原子周围的配位是正方形平面，乙炔配体垂直于Pt平面。关键词：铂配合物，晶体结构，甲基胺，二甲基己炔二醇，合成。