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Triphenyl phosphate (TPhP) is the chemical compound with the formula OP(OC 6 H 5) 3. It is the simplest aromatic organophosphate. This colourless solid is the ester (triester) of phosphoric acid and phenol. It is used as a plasticizer and a fire retardant in a wide variety of settings and products. [3]
Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C 6 H 5) 3 and often abbreviated to P Ph 3 or Ph 3 P. It is versatile compound that is widely used as a reagent in organic synthesis and as a ligand for transition metal complexes, including ones that serve as catalysts in organometallic chemistry.
Triphenyl phosphite is the organophosphorus compound with the formula P(OC 6 H 5) 3. It is a colourless viscous liquid. It is a colourless viscous liquid. Preparation
Ph 3 PO is structurally related to POCl 3. [2] As established by X-ray crystallography, the geometry around P is tetrahedral, and the P-O distance is 1.48 Å. [3] Other modifications of Ph 3 PO have been found: For example, a monoclinic form crystalizes in the space group P2 1 /c with Z = 4 and a = 15.066(1) Å, b = 9.037(2) Å, c = 11.296(3) Å, and β = 98.47(1)°.The orthorhombic ...
Bisphenol A diphenyl phosphate is a halogen-free flame retardant used plastics. It is used in polymer blends of engineering plastics, such as PPO/HIPS and PC/ABS, [1] which are commonly used to make casing for electrical items like TVs, computers and home appliances. It is formed by the transesterification of bisphenol A with triphenyl phosphate.
The reaction mechanism of the Mitsunobu reaction is fairly complex. The identity of intermediates and the roles they play has been the subject of debate. Initially, the triphenyl phosphine (2) makes a nucleophilic attack upon diethyl azodicarboxylate (1) producing a betaine intermediate 3, which deprotonates the carboxylic acid (4) to form the ion pair 5.
One of the first applications of phosphine ligands in catalysis was the use of triphenylphosphine in "Reppe" chemistry (1948), which included reactions of alkynes, carbon monoxide, and alcohols. [16] In his studies, Reppe discovered that this reaction more efficiently produced acrylic esters using NiBr 2 ( PPh 3 ) 2 as a catalyst instead of ...
Tricresyl phosphate (TCP), is a mixture of three isomeric organophosphate compounds most notably used as a flame retardant. [1] Other uses include as a plasticizer in manufacturing for lacquers and varnishes and vinyl plastics and as an antiwear additive in lubricants. Pure tricresyl phosphate is a colourless, viscous liquid, although ...