cis-[Pt(II)(PEt)₃(trifluoromethane-sulfonate)₂] | 165336-82-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机磺酸及其衍生物
• 英文名称: cis-[Pt(II)(PEt)₃(trifluoromethane-sulfonate)₂]
• 英文别名: cis-Pt(PEt₃)2(OTf)₂；cis-(PEt₃)₂Pt(OTf)₂；[Pt(PEt₃)₂(OTf)₂]；Platinum(2+);triethylphosphane;trifluoromethanesulfonate；platinum(2+);triethylphosphane;trifluoromethanesulfonate
• CAS: 165336-82-3
• 化学式: C₁₄H₃₀F₆O₆P₂PtS₂
• 分子量: 729.539
• InChiKey: CKTSPXDXMPQPFT-UHFFFAOYSA-L

计算性质

• 辛醇/水分配系数(LogP)：
  5.16
• 重原子数：
  31
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  131
• 氢给体数：
  0
• 氢受体数：
  12

反应信息

• 作为反应物：
  描述：

  4,4′-偶氮吡啶 、 cis-[Pt(II)(PEt)₃(trifluoromethane-sulfonate)₂] 以 硝基甲烷-d3 为溶剂， 以91%的产率得到
  参考文献：
  名称：

  Effect of ligand flexibility on coordination-driven self-assembly of Pt(II) metallacycles

  摘要：

  The effect of ligand flexibility on the self-assembly of Pt(II) metallacycles was investigated. Three diazopyridyl ligands with different flexibilities were used to synthesize three nanoscale supramolecular complexes via Pt(II) mediated self-assembly. With comparatively less flexible ligands, 4,4'azobispyridine (2) and pyridine-4-carbaldehyde azine (3), formation of [3+3] molecular triangles was observed; in contrast, the most flexible of the three ligands, pyridine-3-carbaldehyde azine (4), yielded the [2+2] molecular rhomboid. All three complexes were characterized by multinuclear NMR (H-1 and P-31) and HR-ESI-MS, and the structure of complex 7 was further established by X-ray crystallography. These studies clearly showed that increased ligand flexibility entropically favors the formation of smaller metallacycles as the ligand can reduce angular strain through bending or conformational change. (C) 2012 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.ica.2012.01.005
• 作为产物：
  描述：

  三乙基膦 以 not given 为溶剂， 生成 cis-[Pt(II)(PEt)₃(trifluoromethane-sulfonate)₂]
  参考文献：
  名称：

  基于腔体的配位笼的自组装和阴离子包封特性

  摘要：

  已经通过自组装程序合成了两种新型的基于腔体的协调笼 7a--j 和 8a--d。控制笼自组装 (CSA) 的主要因素已确定为 (i) 螯合配体和金属前体之间的 P--M--P 角接近 90 度，(ii) Pd 和 Pt 作为金属中心， (iii) 弱配位的反离子，和 (iv) 四齿空腔配体的预组织。量热测量和动态 (1) H 和 (19) F 核磁共振实验表明 CSA 是熵驱动的。平衡笼低聚物的温度范围由空腔组分的预组织水平决定。笼子 7d 的晶体结构显示存在单个被封装的三氟甲磺酸盐阴离子。来宾竞争实验表明，笼子 7b 的封装偏好，d 遵循 BF(4)(-) > CF(3)SO(3)(-) >> PF(6)(-) 在 300 K 的顺序。 ES-MS 实验与分子建模相结合为观察到的提供了基本原理封装选择性。遵循客体溶剂化焓的基本选择性模式会因腔的大小和形状而改变，仅在 BF(4)(-) 的情况下才允许辅助溶剂分子进入。

  DOI：

  10.1021/ja0103492

文献信息

• Molecular Architecture <i>via</i> Coordination:  Self-Assembly, Characterization, and Host−Guest Chemistry of Mixed, Neutral-Charged, Pt−Pt and Pt−Pd Macrocyclic Tetranuclear Complexes. X-ray Crystal Structure of Cyclobis[[<i>cis</i>- Pt(dppp)(4-ethynylpyridine)₂][<i>cis</i>-Pd²⁺(PEt₃)₂2^-OSO₂CF₃]]
  作者：Jeffery A. Whiteford、Cuong V. Lu、Peter J. Stang

  DOI：10.1021/ja9635286

  日期：1997.3.1

  cis-ML2(OSO2CF3)2 (M = Pt or Pd; L = PEt3 or L2 = dppp), in CH2Cl2 or acetone, at room temperature, results in mixed, neutral-charged cyclic tetranuclear, Pt−Pt or Pt−Pd macrocyclic complexes in 90−99% yields via self-assembly. All tetramers are microcrystalline air- and water-stable solids with decomposition points > 170 °C. The benzonitrile based macrocycles can be disassembled in solution with 4,4‘-bipyridine

  顺式 Ptdppp(p-C6H4CN)2 或顺式 Ptdppp(p-C2C6H4N)2 与顺式 ML2(OSO2CF3)2（M = Pt 或 Pd；L = PEt3 或 L2 = dppp）在 CH2Cl2 href=https://www.molaid.com/MS_3163 target="_blank">L2 或丙酮中的相互作用，在室温下，通过自组装产生混合的、带中性电荷的环状四核、Pt-Pt 或 Pt-Pd 大环配合物，产率为 90-99%。所有四聚体都是微晶空气和水稳定的固体，分解点 > 170 °C。基于苯甲腈的大环可以在溶液中与 4,4'-联吡啶分解，而 4-乙炔基吡啶系统对各种客体更稳定。4-乙炔基吡啶四聚体通过“π-镊子效应”显示出与三氟甲磺酸银的主客体化学反应。X 射线晶体结构以及 FABMS，包括同位素模式，
• Syntheses of Pd(ii)/Pt(ii) complexes with non-chelating 4-pyridylselenolate ligand ranging from mononuclear to macrocyclic structures and their utility as catalysts in Suzuki C–C coupling reaction
  作者：K. V. Vivekananda、S. Dey、A. Wadawale、N. Bhuvanesh、V. K. Jain

  DOI：10.1039/c3dt51510a

  日期：——

  respectively. The oxidative addition of bis(4-pyridyl)diselenide to Pt(PPh3)4 exclusively yielded trans-[Pt(4-SeC5H4N)2(PPh3)2] (5b). The treatment of two eq. of Na(4-SeC5H4N) with cis-[PtX2(PR3)2] afforded 5b (X = Cl) and trans-[Pt(4-SeC5H4N)2(PEt3)2] (5c) (X = Cl or CF3SO3). The reactions of cis-[MCl2(P∩P)] and [M2Cl2(μ-Cl)2(PR3)2] with two eq. of Na(4-SeC5H4N) exclusively yielded cis-[M(4-SeC5H4N)2(P∩P)] (M/P∩P

  用双（4-吡啶基）二硒化物处理Na 2 PdCl 4或[MCl 2（PhCN）2 ]，得到的不溶物成分为[MCl 2（4,4'-（C 5 H 4 N）2 Se 2）] n（1）。Na 2 PdCl 4与一当量和两当量的反应。Na（4-SeC 5 H 4 N）的不溶产物[PdCl（4-SeC 5 H 4 N）] n（2）和[Pd（4-SeC 5 H 4 N）2分别为] n（3）。与PPH治疗3，2和3，得到的反式- [的PdCl（4-仲丁基5 ħ 4 N）（PPH 3）2 ]（图4a）和反式- [钯（4-仲丁基5 ħ 4 N）2（PPH 3）2 ]（5a）。双（4-吡啶基）二硒化物向Pt（PPh 3）4的氧化加成仅生成反式-[Pt（4-SeC 5 H 4N）2（PPh 3）2 ]（5b）。两当量的处理。Na（4-SeC 5 H 4 N）与顺式-[PtX 2（PR 3）2 ]的合成得到5b（X
• Cavitand-Based Nanoscale Coordination Cages
  作者：Roberta Pinalli、Veronica Cristini、Valerio Sottili、Silvano Geremia、Mara Campagnolo、Andrea Caneschi、Enrico Dalcanale

  DOI：10.1021/ja038694+

  日期：2004.6.1

  solid-state characterization of nanoscale coordination cages formed by tetradentate cavitand ligands and appropriate metal precursors. The preorganization of the cavitand ligand in terms of structural rigidity and relative orientation of the pyridyl units leads to the exclusive formation of coordination cages in a wide temperature and concentration range. Desired features of the cage self-assembly process,

  该通讯报告了由四齿空腔配体和适当金属前体形成的纳米级配位笼的设计、自组装、解决方案和固态表征。就结构刚性和吡啶基单元的相对取向而言，空腔配体的预组织导致在很宽的温度和浓度范围内独家形成配位笼。已经评估了笼子自组装过程的所需特征，例如存在竞争性配体时的可逆性和腔体组件的自我识别。
• Preparation and Solid-State Properties of Self-Assembled Dinuclear Platinum(II) and Palladium(II) Rhomboids from Carbon and Silicon Tectons
  作者：Marion Schmitz、Stefan Leininger、Jun Fan、Atta M. Arif、Peter J. Stang

  DOI：10.1021/om990567s

  日期：1999.11.1

  hitherto unknown bis(4-pyridyl)silanes 2a,b with bis(triethylphosphine)platinum and bis(triethylphosphine)palladium bistriflates 5a,b lead to the formation of new silicon-containing rhomboids 6a−d. In addition, a similar carbon analogue 7 was prepared by reaction of bispyridyl acetal 4 and bis(triethylphosphine)platinum bistriflate (5a). Surprisingly, reaction of the bis(4-pyridyl)ketone (3) and the platinum

  迄今未知的双（4-吡啶基）硅烷2a，b与双（三乙基膦）铂和双（三乙基膦）钯双三氟甲磺酸酯5a，b的自组装反应导致形成新的含硅菱形6a - d。另外，通过双吡啶基乙缩醛4和双（三乙基膦）铂二铋酸盐（5a）的反应制备了类似的碳类似物7。出乎意料的是，双（4-吡啶基）酮（3）与铂络合物5a的反应产生了类似的菱形10，由于酮的意外水合作用。解析了硅络合物6a及其碳类似物7的晶体结构，并将其与已知的含碳双核菱形进行了比较。另外，还通过X射线结构分析表征了双核双卟啉复合物8。还报告了电喷雾和FAB质谱数据，证实了所形成实体的双核性质。
• Metal Complexes with Very Large Dipole Moments: the Anionic Carborane Nitriles 12-NC–CB₁₁X₁₁^–(X = H, F, CH₃) as Ligands on Pt(II) and Pd(II)
  作者：Filip Šembera、Jan Plutnar、Alexander Higelin、Zbyněk Janoušek、Ivana Císařová、Josef Michl

  DOI：10.1021/acs.inorgchem.5b02678

  日期：2016.4.18

  12-NC-1-H–CB11F10– were prepared, and three of them were examined for complex formation with (Et3P)2Pt(II) and (Et3P)2Pd(II). Several stable internally charge-compensated zwitterionic complexes were obtained and characterized. RI-BP86/SV(P) calculations suggest that their dipole moments exceed 20 D. An attempt to measure the dipole moments in solution failed due to insufficient solubility in solvents of

  阴离子腈1-R-12-NC–CB 11 H 10 –（R = H，CH 3，I，COOH），12-NC-1-H–CB 11 Me 10 –和12-NC-1-制备了H–CB 11 F 10 –，并检查了其中的三个与（Et 3 P）2 Pt（II）和（Et 3 P）2 Pd（II）的络合物形成。获得并表征了几种稳定的内部电荷补偿的两性离子络合物。RI-BP86 / SV（P）计算表明，它们的偶极矩超过20D。由于在低极性溶剂中的溶解度不足，因此无法测量溶液中的偶极矩。