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(Dioxygen)bis(triphenylphosphine)platinum is a chemical compound that consists of a platinum atom coordinated with two triphenylphosphine ligands and two oxygen molecules. It is a versatile and useful compound in the field of organometallic chemistry and catalysis.

15614-67-2

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15614-67-2 Usage

Uses

Used in Chemical Reactions:
(Dioxygen)bis(triphenylphosphine)platinum is used as a catalyst for various chemical reactions, particularly in the oxidation of organic compounds. The presence of the dioxygen ligands allows the compound to participate in oxidative processes, making it a valuable tool in synthetic chemistry.
Used in Organometallic Chemistry:
(Dioxygen)bis(triphenylphosphine)platinum is used as a catalyst in organometallic chemistry, providing stability and solubility to the platinum center, which allows for efficient catalytic activity.

Check Digit Verification of cas no

The CAS Registry Mumber 15614-67-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,6,1 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15614-67:
(7*1)+(6*5)+(5*6)+(4*1)+(3*4)+(2*6)+(1*7)=102
102 % 10 = 2
So 15614-67-2 is a valid CAS Registry Number.

15614-67-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dioxoplatinum,triphenylphosphane

1.2 Other means of identification

Product number -
Other names Dioxobis(triphenylphosphine)platinum(IV)

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:15614-67-2 SDS

15614-67-2Relevant academic research and scientific papers

Structures of transition states in metal-mediated O2-activation reactions

Lanci, Michael P.,Brinkley, David W.,Stone, Kristie L.,Smirnov, Valeriy V.,Roth, Justine P.

, p. 7273 - 7276 (2007/10/03)

(Chemical Equation Presented) Kinetic isotope effects (KIEs) have been used to probe the mechanism of the binding of O2 to classic inorganic compounds. The intermolecular 18O KIEs decrease with increasing rate constants, and the corr

Electrochemical generation and reactivity of bis(tertiary phosphine)platinum(0) complexes: A comparison of the reactivity of [Pt(PPh3)2] and [Pt(PEt3)2] equivalents

Davies, Julian A.,Eagle, Cassandra T.,Otis, Deborah E.,Venkataraman, Uma

, p. 1080 - 1088 (2008/10/08)

Electrochemical reduction of cis-[PtCl2(PR3)2] (R = Ph, Et) in CH3CN/C6H6 containing NBu4ClO4 at a Hg pool electrode generates [Pt(PR3)2] equivalents in solution. Where R = Ph, the [Pt(PR3)2] equivalent may be trapped by O2, O2/CO2, HCl, MeI, C6H5COCl, and RC≡CR (R = Ph, COOMe) but not by the less reactive substrate PhCl. Where R = Et, the [Pt(PR3)2] equivalent reacts with the NBu4+ cation to ultimately generate trans-[PtH(Cl)(PEt3)2]. Prolonged electrolyses cause reduction of trans-[PtH(Cl)(PEt3)2] leading to hydride attack on the CH3CN solvent and ultimately forming trans-[PtH(CH2CN)(PEt3)2]. In the presence of bases such as NBu3, trans-[PtH(CH2CN)(PEt3)2] is isomerized in CH3CN solution producing trans-[PtCN(CH3)(PEt3)2]. The use of electroinactive trapping agents such as PhCl or PhCN as cosolvents for the reduction of cis-[PtCl2(PEt3)2] allows trapping of the [Pt(PEt3)2] equivalents as trans-[PtPh-(X)(PEt3)2] (X = Cl, CN).

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