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词条 Tetrakis(triphenylphosphine)platinum(0)
释义

  1. Structure and behavior

  2. Synthesis and reactions

  3. References

{{chembox
| verifiedrevid = 408887620
| Name = Tetrakis(triphenylphosphine)platinum(0)
| ImageFile = Tetrakis(triphenylphosphine)platinum(0)-3D-sticks.png
| ImageSize = 180px
| ImageName = 3D model of the tetrakis(triphenylphosphine)platinum(0) molecule
| IUPACName = Tetrakis(triphenylphosphane)platinum(0)
| OtherNames = Tetrakis(triphenylphosphane)platinum(0)
TPP platinum(0)
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 14221-02-4
| PubChem = 11979705
| RTECS = Unregistered
| SMILES = c0ccccc0[P+](c0ccccc0)(c0ccccc0)[Pt-4]([P+](c0ccccc0)(c0ccccc0)c0ccccc0)([P+](c0ccccc0)(c0ccccc0)c0ccccc0)[P+](c0ccccc0)(c0ccccc0)c0ccccc0
|Section2={{Chembox Properties
| Formula = {{carbon}}72{{hydrogen}}60{{phosphorus}}4{{platinum}}
| MolarMass = 1244.24 g/mol
| Appearance = yellow crystals
| Density =
| Solubility = Insoluble
| MeltingPtC = 160
|Section3={{Chembox Structure
| MolShape = tetrahedral
| Coordination = four triphenylphosphine unidentate
ligands attached to a central Pt(0)
atom in a tetrahedral geometry
| CrystalStruct =
| Dipole = 0 D
|Section7={{Chembox Hazards
| ExternalSDS = External MSDS
| MainHazards = PPh3 is an irritant
| NFPA-H = 2
| NFPA-F = 1
| NFPA-R =
| RPhrases = n/a
| SPhrases = {{S24/25}}
|Section8={{Chembox Related
| OtherFunction_label = complexes
| OtherFunction = Tetrakis(triphenylphosphine)palladium(0)
tetrakis(triphenylphosphine)nickel(0)
tris(triphenylphosphine)platinum(0)
| OtherCompounds = triphenylphosphine
}}Tetrakis(triphenylphosphine)platinum(0) is the chemical compound with the formula Pt(P(C6H5)3)4, often abbreviated Pt(PPh3)4. The bright yellow compound is used as a precursor to other platinum complexes.[1][2]

Structure and behavior

The molecule is tetrahedral, with point group symmetry of Td, as expected for a four-coordinate metal complex of a metal with the d10 configuration.[3] Even though this complex follows the 18 electron rule, it dissociates triphenylphosphine in solution to give the 16e derivative containing only three PPh3 ligands:

Pt(PPh3)4 → Pt(PPh3)3 + PPh3

Synthesis and reactions

The complex is typically prepared in one-pot reaction from potassium tetrachloroplatinate(II). Reduction of this platinum(II) species with alkaline ethanol in the presence of excess triphenylphosphine affords the product as a precipitate. The reaction occurs in two distinct steps. In the first step, PtCl2(PPh3)2 is generated. In the second step, this platinum(II) complex is reduced. The overall synthesis can be summarized as:

K2[PtCl4] + 2KOH + 4PPh3 + C2H5OH → Pt(PPh3)4 + 4KCl + CH3CHO + 2H2O

Pt(PPh3)4 reacts with oxidants to give platinum(II) derivatives:

Pt(PPh3)4 + Cl2cis-PtCl2(PPh3)2 + 2 PPh3

Mineral acids give the corresponding hydride complexes:

Pt(PPh3)4 + HCl → trans-PtCl(H)(PPh3)2 + 2 PPh3

The reaction with oxygen affords a dioxygen complex:

Pt(PPh3)4 + O2 → Pt(η2-O2)(PPh3)2 + 2 PPh3

This complex is a precursor to the ethylene complex

Pt(η2-O2)(PPh3)2 + C2H4 → Pt(η2-C2H4)(PPh3)2 + "NaBH2(OH)2"

References

1. ^{{cite journal | journal = Inorganic Syntheses | volume = 28 |author1=Ugo, R. |author2=Cariati, F. |author3=La Monica, G. | title = Tris- and tetrakis(triphenylphosphine)platinum(0)| pages = 123–126 | doi = 10.1002/9780470132593.ch33 | year = 1990}}
2. ^Safety Data Sheet http://www.alfa.com/content/msds/english/10549.pdf
3. ^Miessler, Gary L., and Donald A. Tarr. Inorganic Chemistry. 3rd ed. Upper Saddle River, NJ: Pearson Prentice Hall, 2004.
{{Platinum compounds}}

5 : Platinum compounds|Catalysts|Homogeneous catalysis|Triphenylphosphine complexes|Coordination compounds

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