Pt(PiPr3)3 | 60648-72-8

• 分子结构分类: 有机化合物 - 有机磷化合物 - 有机膦及其衍生物
• 英文名称: Pt(PiPr3)3
• 英文别名: Platinum;tri(propan-2-yl)phosphane；platinum;tri(propan-2-yl)phosphane
• CAS: 60648-72-8
• 化学式: C₂₇H₆₃P₃Pt
• 分子量: 675.798
• InChiKey: PZMAMIXVQQEOEM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  11.08
• 重原子数：
  31
• 可旋转键数：
  9
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  Pt(PiPr3)3 反应 1.0h， 生成 [Pt(PiPr3)2]
  参考文献：
  名称：

  Diboran（4）yl配体的强反式影响的证据

  摘要：

  乙硼烷（4）基的Pt II 络合物：选择性氧化加成一个B的我键在乙2（NME 2）2我2至[PT（P我镨3）2 ]，得到一个反-diboran（4）基铂（ II）络合物（参见方案; Ar F = 3,5-（CF 3）2 C 6 H 3）。比较其溴类似物和相关物种的PtI键长度和PtBr键长度可评估配体的反式影响。这反式影响使卤化物易于提取生成T型14电子二硼烷（4）基铂（II）配合物。

  DOI：

  10.1002/chem.201203220
• 作为产物：
  描述：

  trans-dichlorobis(tri-isopropylphosphine)platinum(II) 、 三异丙基膦 在 K#Hg 作用下， 以 四氢呋喃 为溶剂， 以21%的产率得到Pt(PiPr3)3
  参考文献：
  名称：

  甲31的结构中，平衡，和动力学的对核磁共振调查[PT（PR 3）Ñ ]在溶液中

  摘要：

  化合物[专利文献4 ]（L = PME 3，PME 2 PH，PMePh 2，PET 3，或PBU Ñ 3），[专利文献3 ] [L = PET 3，PBU Ñ 3，P（p -甲苯基）3， P（CH 2 Ph）3，PPr i 3或P（C 6 H 11）3 ]和[PtL 2 ] [L = PPr i 3，P（C 6 H 11）3或PBu t 2已制备[Ph]并显示其存在于溶液中。在L = PMePh 2，PEt 3，PBu n 3，n = 3且L = PPr i 3，P（C 6 H 11）3，n = 2的情况下，已证明可以测量平衡常数ΔH ⊖，Δ小号⊖对于专利文献ñ 1 ] ⇌ [PTL ñ ] + L的[PT（PME 3）4 ]，[铂（PME 2 PH）4 ]，[铂（PMePh 2）4]，[Pt（PEt 3）4 ]，[Pt（PBu n 3）4 ]，[Pt（PPr i 3）3 ]和[Pt {P（C

  DOI：

  10.1039/dt9800000776

文献信息

• Correlations and Contrasts in Homo- and Heteroleptic Cyclic (Alkyl)(amino)carbene-Containing Pt⁰Complexes
  作者：Nicole Arnold、Holger Braunschweig、Peter B. Brenner、Mehmet Ali Celik、Rian D. Dewhurst、Martin Haehnel、Thomas Kramer、Ivo Krummenacher、Todd B. Marder

  DOI：10.1002/chem.201502048

  日期：2015.8.24

  route to homoleptic complex [Pt(CAACMe)2] (CAAC=cyclic (alkyl)(amino)carbenes) and convenient routes to new heteroleptic complexes of the form [Pt(CAACMe)(PR3)] are presented. Although the homoleptic complex was found to be inert to many reagents, oxidative addition and metal‐only Lewis pair (MOLP) formation was observed from one of the heteroleptic complexes. The spectroscopic, structural, and electrochemical

  提出了一种改进的合成方法，制备了均相复合物[Pt（CAAC Me）2 ]（CAAC =环（烷基）（氨基）碳烯），并便捷地合成了新的[Pt（CAAC Me）（PR 3）形式的杂合复合物。。尽管发现同型配合物对许多试剂均呈惰性，但从其中一种杂合剂配合物中观察到了氧化加成反应和仅金属路易斯对（MOLP）的形成。与密度泛函理论（DFT）和时变密度泛函理论（TD-DFT）计算一起探索了零价配合物的光谱，结构和电化学性质。同功[Pt（CAAC）2 ]和同功[Pt（CAAC）（PR 3）]发现配合物的光谱和结构性质相似，但它们的电化学行为和反应性差异很大。通过TD-DFT计算研究了含CAAC的Pt 0配合物异常强的颜色，这归因于配合物的LUMO激发，其主要由Pt和CAAC碳原子之间的键π相互作用组成。
• Reactivity of Tetrahalo- and Difluorodiboranes(4) toward Lewis Basic Platinum(0): Bis(boryl), Borylborato, and Doubly Boryl-Bridged Platinum Complexes
  作者：Jonas H. Muessig、Dominic Prieschl、Andrea Deißenberger、Rian D. Dewhurst、Maximilian Dietz、J. Oscar C. Jiménez-Halla、Alexandra Trumpp、Sunewang R. Wang、Carina Brunecker、Alena Haefner、Annalena Gärtner、Torsten Thiess、Julian Böhnke、Krzysztof Radacki、Rüdiger Bertermann、Todd B. Marder、Holger Braunschweig

  DOI：10.1021/jacs.8b08428

  日期：2018.10.10

  9-anthryl) toward a range of platinum(0) complexes was investigated. Reactions with relatively nonbulky platinum(0) complexes led to the formation of unsymmetrical cis-bis(boryl) complexes cis-[(R3P)2Pt(BF2)(BMes2)] (6, R = Me; 7, R = Et) as well as the first example of a fourfold-unsymmetrical bis(boryl) complex, [(Me3P)(Cy3P)Pt(BF2)(BMes2)] (12). The use of a more bulky Pt complex provided access to the

  四卤代二硼烷 (4) B2F4、B2Cl4 和 B2Br4 与路易斯碱性铂 (0) 络合物的反应导致分离了顺式双（二氟硼基）络合物 cis-[(Cy3P)2Pt(BF2)2] (1 ) 和新型硼酸硼络合物反式-[(Cy3P)2PtB(X)-BX3}] (2, X = Cl; 3, X = Br)，分别。硼酸硼基团的反式影响被发现是有史以来在实验中观察到的最强的影响之一。此外，研究了很少探索的二芳基二氟二硼烷 (4) F2B-BMes2 和新衍生物 F2B-BAn2 (An = 9-蒽基) 对一系列铂 (0) 配合物的反应性。与相对体积较小的铂 (0) 配合物的反应导致形成不对称的顺式双(硼基) 配合物 cis-[(R3P)2Pt( )(BMes2)] (6, R = Me; 7, R = Et) 作为以及四重不对称双（硼酸）络合物的第一个例子，[(Me3P)(Cy3P)Pt( )(BMes2)]
• New Metal-Only Lewis Pairs: Elucidating the Electronic Influence of<i>N</i>-Heterocyclic Carbenes and Phosphines on the Dative Pt-Al Bond
  作者：Jürgen Bauer、Rüdiger Bertermann、Holger Braunschweig、Katrin Gruss、Florian Hupp、Thomas Kramer

  DOI：10.1021/ic300531b

  日期：2012.5.21

  N-heterocyclic carbene (NHC)–phosphine platinum(0) complex and formation of its corresponding alane adduct is reported. The influence of the ligands on the Lewis basic properties was studied via multinuclear NMR-spectroscopy, X-ray analyses, and density functional theory (DFT) calculations. Consistently, the effect of changing the halogens upon the Lewis acid properties of aluminum halides was studied by

  报道了新型杂合N-杂环卡宾（NHC）-膦铂（0）配合物的合成和完整特征，以及其相应的烷烃加合物的形成。通过多核NMR光谱，X射线分析和密度泛函理论（DFT）计算研究了配体对Lewis基本性质的影响。一致地，通过X射线分析和DFT计算研究了改变卤素对卤化铝的路易斯酸性质的影响。
• Investigation of Steric Factors Involved in the Formation of Terminal Cationic Platinum Arylborylene Complexes
  作者：Nicole Arnold、Holger Braunschweig、Peter B. Brenner、Rian Dewhurst、Thomas Kramer、Krzysztof Radacki

  DOI：10.1021/om501141g

  日期：2015.6.8

  6-tetramethylphenyl) groups. Halide abstraction from the 4-tert-butylphenyl complex resulted in a T-shaped cationic boryl complex. However, subjecting the duryl-substituted complexes to the same conditions exclusively results in terminal cationic borylene complexes, a difference we attribute to the greater steric hindrance between the boron-bound bromide and the methyl groups at the 2- and 6-positions of the

  以前已显示从Pt II二膦硼烷基络合物中提取卤代配体可产生两种异构产物之一：T形阳离子硼基络合物或方平面阳离子硼基络合物。然而，仅在一种情况下观察到后一种产物，即间苯二甲酰基配体的产物，其在卤代夺去时转化为间苯二甲烯基配体。为了在不同的空间和电子影响下测试该反应的效力，制备了具有4-叔丁基苯基和duryl（2,3,5,6-四甲基苯基）基团的Pt II二膦硼烷基配合物。从4叔抽象卤化物丁基苯基络合物产生T形阳离子硼基络合物。但是，将duryl取代的配合物置于相同条件下只会导致末端阳离子亚芳基配合物，我们的差异归因于结合硼的溴化物与duryl的2位和6位甲基之间的较大位阻团体。该结果表明在对位的烷基化的电子效应不是该亚芳基形成反应的因素。
• Syntheses and Structures of Alkyl and Aryl Halide Complexes of the Type [(PiPr₃)₂PtH(η¹-XR)]BAr_f and Analogues with Et₂O, THF, and H₂ Ligands. Halide-to-Metal π Bonding in Halocarbon Complexes
  作者：Matthew D. Butts、Brian L. Scott、Gregory J. Kubas

  DOI：10.1021/ja961836y

  日期：1996.1.1

  The reaction of Pt(PiPr(3))(3) with SO2 led to the formation of (PiPr(3))(2)Pt(SO2) (1), isolated in 93% yield. The addition of [H(OEt(2))(2)](BArf)-B-+(BArf = B(3,5-(CF3)(2)C6H3)(4)) to 1 in ether at -78 degrees C afforded the solvent complex trans-[(PiPr(3))(2)Pt(H)(OEt(2))]BArf (2) in 85% isolated yield. Complex 2 served as a precursor to monodentate halocarbon complexes of the type Pt(eta(1)-XR). The dichloromethane complex trans-[(PiPr(3))(2)Pt(H)(eta(1)-ClCH2Cl)]BArf (3) was isolated in 80% yield by the recrystallization of 2 from CH2Cl2/hexane. IR spectroscopy suggested the existence of dichloromethane binding which was confirmed by X-ray crystallography. The reaction of 2 or 3 with iodo- or bromobenzene led to the isolation of the haloarene complexes trans-[(PiPr(3))(2)Pt(H)(eta(1)-XPh)]BArf, where X = I (4, 87% yield) or Br (5, 60% yield). Both compounds were characterized spectroscopically and by X-ray crystallography. An unexpected steric interaction in 4, suggested by molecular mechanics calculations to be significant, was rationalized in terms of halide-to-metal pi bonding. The PhI complex 4 decomposed under harsh conditions to the bridging iodide compound trans-[(PiPr(3))(2)Pt(H)](2)(mu-I)}BArf (6) which was structurally characterized. The THF adduct [(PiPr(3))(2)Pt(H)(THF)]BArf (7), isolated in 78% yield and also characterized by X-ray crystallography, was formed when any of the compounds 2, 3, 4, or 5 was dissolved in THF. The CH2Cl2 complex 3 reacted with H-2 to form the dihydrogen complex tans-[(PiPr(3))(2)Pt(H)(eta(2)-H-2)]BArf which was characterized by NMR spectroscopy.