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14221-02-4

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14221-02-4 Usage

Chemical Properties

yellow powder

Uses

Tetrakis(triphenylphosphine)platinum(0), Pt is widely used in hydrosilation and oxidation. In Catalysts, Metal & Specialty Catalysts, Products & Industries.

Purification Methods

It forms yellow crystals on adding hexane to a cold saturated solution in *C6H6. It is soluble in *C6H6 and CHCl3 but insoluble in EtOH and hexane. A less pure product is obtained if it is crystallised by adding hexane to a CHCl3 solution. It is stable in air for several hours and completely stable under N2. [Malatesta & Cariello J Am Chem Soc 2323 1958, Beilstein 16 IV 955.]

Check Digit Verification of cas no

The CAS Registry Mumber 14221-02-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,2 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14221-02:
(7*1)+(6*4)+(5*2)+(4*2)+(3*1)+(2*0)+(1*2)=54
54 % 10 = 4
So 14221-02-4 is a valid CAS Registry Number.
InChI:InChI=1/4C18H15P.Pt/c4*1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;/h4*1-15H;/q;;;;-4/p+4/rC72H64P4Pt/c1-13-37-61(38-14-1)73(62-39-15-2-16-40-62,63-41-17-3-18-42-63)77(74(64-43-19-4-20-44-64,65-45-21-5-22-46-65)66-47-23-6-24-48-66,75(67-49-25-7-26-50-67,68-51-27-8-28-52-68)69-53-29-9-30-54-69)76(70-55-31-10-32-56-70,71-57-33-11-34-58-71)72-59-35-12-36-60-72/h1-60,73-76H

14221-02-4 Well-known Company Product Price

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  • Alfa Aesar

  • (10549)  Tetrakis(triphenylphosphine)platinum(0), Pt 15.2% min   

  • 14221-02-4

  • 1g

  • 1300.0CNY

  • Detail
  • Alfa Aesar

  • (10549)  Tetrakis(triphenylphosphine)platinum(0), Pt 15.2% min   

  • 14221-02-4

  • 5g

  • 5788.0CNY

  • Detail
  • Aldrich

  • (244961)  Tetrakis(triphenylphosphine)platinum(0)  97%

  • 14221-02-4

  • 244961-1G

  • 1,278.81CNY

  • Detail
  • Aldrich

  • (244961)  Tetrakis(triphenylphosphine)platinum(0)  97%

  • 14221-02-4

  • 244961-5G

  • 4,415.58CNY

  • Detail

14221-02-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetrakis(triphenylphosphine)platinum(0)

1.2 Other means of identification

Product number -
Other names Platinum(0)-tetrakis(triphenylphosphine)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:14221-02-4 SDS

14221-02-4Relevant articles and documents

The synthesis and vibrational spectra of tetrakistrimethylphosphinenickel(0) and -platinum(0), Ni(PMe3)4 and Pt(PMe3)4

Edwards, H. G. M.

, p. 1401 - 1404 (1986)

The syntheses of the molecules Ni(PMe3)4 and Pt(PMe3)4 are reported for the first time.The platinum compound is much less stable than the nickel analogue.Raman and i.r. spectra have been obtained for the nickel compound and a complete vibrational assignment is proposed on the basis of Td molecular symmetry.For the platinum compound only the i.r. spectrum has been obtained.

Method for preparing palladium (0) or platinum (0) composite compound from triphenylphosphine

-

Paragraph 0033; 0034, (2019/01/08)

The invention provides a method for preparing a palladium (0) or platinum (0) composite compound from triphenylphosphine; with use of palladium chloride (PdCl2) or hydrochloroplatinic acid (H2PtCl6.xH2O) as a starting material, preliminary preparation reaction is not needed, and commercially purchased palladium chloride or hydrochloroplatinic acid can be directly used for reaction. The reaction process is simple, all the reactions are carried out in a same reactor, separation of intermediate products is not needed, and the loss is reduced; the yield of target products is high; the recovery problem of reaction residues is simplified. The product has high reactivity and catalytic activity in various reactions, and has broad application prospects.

Si-H bond activation by (Ph3P)2Pt(η2- C2H4) in dihydrosilicon tricycles that also contain O and N heteroatoms

Braddock-Wilking, Janet,Corey, Joyce Y.,French, Lisa M.,Choi, Eunwoo,Speedie, Victoria J.,Rutherford, Michael F.,Yao, Shu,Xu, Huan,Rath, Nigam P.

, p. 3974 - 3988 (2008/10/09)

Several tricyclic phenoxasilin and phenazasiline heterocycles were synthesized from the corresponding 2,2′-dilithio-diphenyl ether or diphenyl amine precursor and silicon tetrachloride (or trichlorosilane) followed by reduction with lithium aluminum hydride [H2SiAr2: Ar2 = C12H8O (1); Ar2 = C 14H12O (2); Ar2 = C13H11N (3); Ar2 = C15H15N (4); Ar2 = C13H9Br2N (5)]. The reactivity of hydrosilanes 1-5 with (Ph3P)2Pt(η2-C2H 4) (6) was investigated. At room temperature, mononuclear complexes, (Ph3P)2Pt(H)-(SiAr2H) and (Ph 3P)2Pt(SiAr2H)2, were generally observed by NMR spectroscopy but were too reactive or unstable to isolate. Dinuclear and in some cases trinuclear Pt-Si-containing complexes were observed as the major products from the reactions. Symmetrical dinuclear complexes, [(Ph3P)Pt(μ-η2-H-SiAr2)]2 (8 and 22, respectively), were produced from the reaction of 1 or 3 with 6. In contrast, reaction of silane 2 with 6 produced a trinuclear complex, [(Ph 3P)Pt(μ-SiAr2)]3 (16), as the major product. However, reaction of 4 or 5 with complex 6 produced an unsymmetrical dinuclear complex, [(Ph3P)2Pt(H)(μ-SiAr2)(μ- η2-H-SiAr2)Pt(PPh3)] (26 and 30, respectively), as the major component. The molecular structures of a symmetrical (22) and unsymmetrical dinuclear (30) complex as well as a trinuclear (16) complex were determined by X-ray crystallography.

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