cis-[Me₂Pt{P(OPh)₃}₂] | 548767-99-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: cis-[Me₂Pt{P(OPh)₃}₂]
• 英文别名: cis-[PtMe2(P(OPh)3)2]；Carbanide;platinum(2+);triphenyl phosphite；carbanide;platinum(2+);triphenyl phosphite
• CAS: 548767-99-3
• 化学式: C₃₈H₃₆O₆P₂Pt
• 分子量: 845.728
• InChiKey: QBMGFWGAYBHCSZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  11.8
• 重原子数：
  47
• 可旋转键数：
  12
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  55.4
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  亚磷酸三苯酯 、 bis[dimethyl(μ-dimethylsulfide)platinum(II)] 以 苯 为溶剂， 以99%的产率得到cis-[Me₂Pt{P(OPh)₃}₂]
  参考文献：
  名称：

  Organoplatinum(II) complexes with phosphite ligands

  摘要：

  The phosphite complexes cis-[PtMe2L(SMe2)] in which L = P((OPr)-Pr-i)(3), 1a, or L = P(OPh)(3), 1b, were synthesized by the reaction of cis, cis-[Me2Pt(mu-SMe2)(2)PtMe2] with 2 equiv. of L. If 4 equiv. of L was used the bis-phosphite complexes cis-[PtMe2L2] in which L = P((OPr)-Pr-i)(3), 2a, or L = P(OPh)(3), 2b, were obtained. The reaction of cis-[Pt(p-MeC6H4)(2)(SMe2)(2) ] with 2 equiv. of L gave the aryl bis-phosphite complexes cis[ Pt(p-MeC6H4)(2)L-2] in which L = P((OPr)-Pr-i)(3), 2a', or L = P(OPh)(3), 2b'. Use of 1 equiv. of L in the latter reaction gave the bis-phosphite complex along with the starting complex in a 1:1 ratio.The complexes failed to react with MeI. The reaction of cis, cis-[Me2Pt(mu-SMe2)(2)PtMe2] with 2 equiv. of the phosphine PPh3 gave cis-[PtMe2(PPh3)(2)] and cis-[PtMe2(PPh3)(SMe2)] along with unreacted starting material. Reaction of cis-[PtMe2L(SMe2)], 1a and 1b with the bidentate phosphine ligand bis(diphenylphosphino) methane, dppm = Ph2PCH2PPh2, gave [PtMe2(dppm)], 8, along with cis-[PtMe2L2], 2. The reaction of cis-[PtMe2L(SMe2)] with 1/ 2 equiv. of the bidentate N-donor ligand NN = 4,4'-bipyridine yielded the binuclear complexes [PtMe2L(mu-NN)PtMe2L] in which L = P((OPr)-Pr-i)(3), 3a, or L = P(OPh)(3), 3b. The complexes were fully characterized using multinuclear NMR (H-1, C-13, P-31, and Pt-195) spectroscopy. (C) 2008 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.jorganchem.2008.04.034

文献信息

• Substitution and cyclometallation reactions on Pt(II) phosphite complexes
  作者：Mahboubeh Jamshidi、Hamidreza Samouei、Ahmad R. Esmaeilbeig

  DOI：10.1016/j.jorganchem.2016.04.028

  日期：2016.7

  paper describes the formation of newseries of platinum(II) complexes with phosphite and phosphine ligands. Treatment of cis,cis-[Me2Pt(μ-SMe2)2PtMe2] with 2 equimolar of L, L = P(OiPr)3orP(OPh)3, then adding 2 equimolar of L′, L′ = PPh3 or 4-MePy, gavecis-[Me2PtLL′] complexes,1a–4a, with some side products. Otherwise, reaction of cis,cis-[Me2Pt(μ-SMe2)2PtMe2] with 4 equimolar of Me2SO, then adding 2

  本文介绍了具有亚磷酸酯和膦配体的新系列铂（II）配合物的形成。的治疗顺，顺- [我2的Pt（μ -SMe 2）2 PTME 2 ]与等摩尔2升，L = P（O我PR）3或P（OPH）3，然后加入等摩尔的2升'，L '= PPh 3或4-MePy，得到顺式[[Me 2 PtLL']配合物1a - 4a，带有一些副产物。否则，顺式，顺式-[Me 2 Pt（μ- SMe 2）2PtMe 2 ]与4等摩尔的Me 2 SO，然后添加2等摩尔的PPh 3，得到顺式-[Me 2 Pt（Me 2 SO- κS）（PPh 3）]。加入1等摩尔的L，L ＝ P（OPh）3和P（O i Pr）3并取代Me 2 SO，得到具有更高选择性的顺式-[Me 2 PtLL']复合物2a和4a。为了控制配体的空间和电子效应，将2和4等摩尔的P（OPh）3添加到顺，顺-[Me2的Pt（μ -SMe 2）2 PTME 2 ]中
• Organoplatinum(II) complexes with phosphite ligands
  作者：Ahmad R. Esmaeilbeig、Hamid R. Samouei、Mehdi Rashidi

  DOI：10.1016/j.jorganchem.2008.04.034

  日期：2008.7

  The phosphite complexes cis-[PtMe2L(SMe2)] in which L = P((OPr)-Pr-i)(3), 1a, or L = P(OPh)(3), 1b, were synthesized by the reaction of cis, cis-[Me2Pt(mu-SMe2)(2)PtMe2] with 2 equiv. of L. If 4 equiv. of L was used the bis-phosphite complexes cis-[PtMe2L2] in which L = P((OPr)-Pr-i)(3), 2a, or L = P(OPh)(3), 2b, were obtained. The reaction of cis-[Pt(p-MeC6H4)(2)(SMe2)(2) ] with 2 equiv. of L gave the aryl bis-phosphite complexes cis[ Pt(p-MeC6H4)(2)L-2] in which L = P((OPr)-Pr-i)(3), 2a', or L = P(OPh)(3), 2b'. Use of 1 equiv. of L in the latter reaction gave the bis-phosphite complex along with the starting complex in a 1:1 ratio.The complexes failed to react with MeI. The reaction of cis, cis-[Me2Pt(mu-SMe2)(2)PtMe2] with 2 equiv. of the phosphine PPh3 gave cis-[PtMe2(PPh3)(2)] and cis-[PtMe2(PPh3)(SMe2)] along with unreacted starting material. Reaction of cis-[PtMe2L(SMe2)], 1a and 1b with the bidentate phosphine ligand bis(diphenylphosphino) methane, dppm = Ph2PCH2PPh2, gave [PtMe2(dppm)], 8, along with cis-[PtMe2L2], 2. The reaction of cis-[PtMe2L(SMe2)] with 1/ 2 equiv. of the bidentate N-donor ligand NN = 4,4'-bipyridine yielded the binuclear complexes [PtMe2L(mu-NN)PtMe2L] in which L = P((OPr)-Pr-i)(3), 3a, or L = P(OPh)(3), 3b. The complexes were fully characterized using multinuclear NMR (H-1, C-13, P-31, and Pt-195) spectroscopy. (C) 2008 Elsevier B.V. All rights reserved.