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Tetraphenyldiphosphine oxide (TPPO) is a chemical compound with the formula (C6H5)2P(O)P(C6H5)2. It is a white crystalline solid that is soluble in organic solvents. TPPO is an important organophosphorus compound, widely used as a ligand in coordination chemistry, particularly in the synthesis of transition metal complexes. It is also employed as a reagent in organic synthesis, a stabilizer for various materials, and a flame retardant. Due to its unique structure and properties, TPPO has attracted significant attention in the fields of catalysis, materials science, and pharmaceuticals.

2096-83-5

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2096-83-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2096-83-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,9 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2096-83:
(6*2)+(5*0)+(4*9)+(3*6)+(2*8)+(1*3)=85
85 % 10 = 5
So 2096-83-5 is a valid CAS Registry Number.

2096-83-5Relevant academic research and scientific papers

Highly Selective Phosphinylphosphination of Alkenes with Tetraphenyldiphosphine Monoxide

Sato, Yuki,Kawaguchi, Shin-Ichi,Nomoto, Akihiro,Ogawa, Akiya

, p. 9700 - 9703 (2016)

In sharp contrast to tetraphenyldiphosphine, which does not add to carbon–carbon double bonds efficiently, its monoxide, [Ph2P(O)PPh2] can engage in a radical addition to various alkenes, thus affording the corresponding 1-phosphinyl-2-phosphinoalkanes regioselectively, and they can be converted into their sulfides by treatment with elemental sulfur. The phosphinylphosphination proceeds by the homolytic cleavage of the PV(O)?PIIIsingle bond of Ph2P(O)PPh2, followed by selective attack of the phosphinyl radical at the terminal position of the alkenes, and selective trapping of the resulting carbon radical by the phosphino group. Furthermore, the phosphinylphosphination product could be converted directly into its platinum complex with a hemilabile P,O chelation.

Chemistry of Polyfunctional Molecules CXXVI [1]. Synthesis, Structure, and Tautomerism of 5-Fluoro-N(1),N(3)-bis(diphenylphosphanyl)uracil

Ellermann,Schamberger,Knoch,Moll,Bauer

, p. 399 - 410 (1997)

5-Fluoro-uracil (1) reacts with chloro-diphenylphosphane to 5-fluoro-N(1), N(3)-bis-(diphenylphosphanyl)uracil (3) which was characterized by X-ray crystallography, IR, and mass spectra. 19F, 31P{1H}, 13C{1

Rhodium-catalyzed synthesis of 1-alkynylphosphine oxides from 1-alkynes and tetraphenylbiphosphine

Arisawa, Mieko,Onoda, Masato,Hori, Chieko,Yamaguchi, Masahiko

, p. 5211 - 5213 (2006)

A rhodium complex RhH(PPh3)4 catalyzes the C-P bond forming reaction of 1-alkynes and tetraphenylbiphosphine in the presence of 2,4-dimethylnitrobenzene giving 1-alkynylphosphines and its oxides.

Indium(III) promoted oxidative P-P coupling of silylphosphines

Cartlidge, Ashleigh J.,Matthews, Peter D.

, (2022/01/28)

The reaction of indium(III) salts with Ph2PSiMe3 and PhP(SiMe3)2 gives rise to a one- and two-electron reductive P-P coupling respectively, with the formation of new P-P bonds resulting in the preparation of (Ph2P)2 and the cyclicoligophosphane compounds (PhP)4 and (PhP)6.

An approach towards the synthesis of lithium and beryllium diphenylphosphinites

Berthold, Chantsalmaa,Thomas-Hargreaves, Lewis R.,Ivlev, Sergei I.,Buchner, Magnus R.

, p. 651 - 658 (2021/10/12)

The diphenylphosphinites [(THF)Li(OPPh2)]4 and [(THF)2Be(OPPh2)2] have been synthesized via direct deprotonation of diphenylphosphine oxide with n BuLi and BePh2, respectively, as well as via salt metathesis. These compounds were characterized by multinuc

Photoinduced Coupling Reaction of Diphenyl(2,4,6-trimethylbenzoyl)phosphine Oxide with Interelement Compounds: Application to the Synthesis of Thio- or Selenophosphinates

Sato, Yuki,Kawaguchi, Shin-Ichi,Nomoto, Akihiro,Ogawa, Akiya

, p. 3558 - 3567 (2017/08/16)

Diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TMDPO) is a radical initiator widely used in the field of macromolecular chemistry, but not often applied in synthetic organic chemistry. We have focused on the use of TMDPO as a phosphorus source in reactions with different E - E compounds, where E - E represents a heteroatom-heteroatom bond, under photoirradiation. Interestingly, the cross-coupling reaction between TMDPO and disulfides or diselenides successfully affords thio- or selenophosphinates and thio- or selenoesters, respectively. The synthesis of series of thio- and selenophosphinates by this photoinduced cross-coupling reaction is demonstrated.

PHOSPHINE COMPOUND HAVING PERFLUORO GROUP, AND COMPLEX BETWEEN METAL AND PHOSPHINE HAVING PERFLUORO GROUP

-

, (2018/10/16)

PROBLEM TO BE SOLVED: To provide a perfluoroalkylphosphine compound, and a complex between a metal and the perfluoroalkylphosphine. SOLUTION: A perfluoroalkylphosphine compound is a phosphine compound represented by the general formula Rf-PR1R2. In the formula, R1 and R2 are each independently a substituted or unsubstituted hydrocarbon group; Rf is a perfluorinated hydrocarbon group. Also provided is a complex between the perfluoroalkylphosphine and a phosphine coordination metal. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

METHODS OF PRODUCING PHOSPHINE COMPOUND HAVING PERFLUORO GROUP AND COMPLEX BETWEEN METAL AND PHOSPHINE HAVING PERFLUORO GROUP

-

Paragraph 0152, (2018/10/19)

PROBLEM TO BE SOLVED: To provide methods of producing a perfluoroalkylphosphine compound improved in a phosphorus element yield and a chemical yield. SOLUTION: A method of producing a perfluoroalkylphosphine compound comprises either reacting a perfluoroalkyl iodide with, e.g., 2,4,6-trimethylbenzoyldiphenylphosphine oxide (TMDPO) or a triarylphosphine such as triphenylphosphine, which are easily available, in the presence of a radical generator such as azobis(isobutyronitrile) or light irradiation, or reacting TMDPO or the like with perfluoroalkyl iodide in the presence of diphenylphosphine, diethylphosphine, dicyclohexylphosphine or the like. SELECTED DRAWING: None COPYRIGHT: (C)2016,JPOandINPIT

Mixed anhydride complexes of rhodium(i) and ruthenium(ii)-their synthesis and ligand rearrangements

Coetzee, Jacorien,Eastham, Graham R.,Slawin, Alexandra M. Z.,Cole-Hamilton, David J.

, p. 3479 - 3491 (2014/03/21)

The coordination chemistry and solution behaviour of Rh(i) and Ru(ii) complexes derived from mixed anhydride ligands of carboxylic acids and phosphorus acids were explored. Similar to the free ligand systems, mixed anhydride complexes rearranged in solution via a number of pathways, with the pathway of choice dependent on the mixed anhydride employed, the auxiliary ligands present as well as the nature of the metal centre. Plausible mechanisms for some of the routes of rearrangement and by-product formation are proposed. Where stability allowed, new complexes were fully characterised, including solid state structures for four of the unrearranged mixed anhydride complexes and two of the interesting rearrangement products.

Phosphane ligands with enaminoketone scaffold and their palladium complexes

Schmidt, Michael,Heck, Juergen

experimental part, p. 1151 - 1158 (2012/07/28)

The reaction of (Z)-4-aminopent-3-en-2-one with different chlorodiorganylphosphanes established three new ligands composed of a hard and soft coordination site. The soft phosphane site is easily coordinated to palladium(II) as a first step in the potential formation of heterodinuclear complexes. Surprisingly, the formed square-planar dichloridopalladium(II) complexes exhibit exclusively trans configuration. A cis configurated palladium(II) complex can be formed, when the linker between the phosphane and the enaminoketone unit is enlarged and allows more flexibility. The reaction between (Z)-4-(2'-hydroxyethylamino)pent-3-en-2-one and chlorodiorganylphosphanes revealed two new ligands that coordinate to palladium(II). With phenyl substituents at the phosphorus atom a cis palladium complex was obtained, whereas for isopropyl substituents a trans complex was formed. Molecular structures of all complexes were analyzed by single-crystal X-ray diffraction.

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