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  2. Triphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine

    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.

  3. Triphenylphosphine oxide - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine_oxide

    It is poorly soluble in hexane and cold diethyl ether. Trituration or chromatography of crude products with these solvents often leads to a good separation of triphenylphosphine oxide. Its removal is facilitated by conversion to its Mg(II) complex, which is poorly soluble in toluene or dichloromethane and can be filtered off. [7]

  4. Triphenylphosphine sulfide - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine_sulfide

    Triphenylphosphine sulfide (IUPAC name: triphenyl-λ 5-phosphanethione) is the organophosphorus compound with the formula (C 6 H 5) 3 PS, usually written Ph 3 PS (where Ph = phenyl). It is a colourless solid, which is soluble in a variety of organic solvents. Structurally, the molecule resembles the corresponding oxide, with idealized C 3 point ...

  5. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.

  6. Wilkinson's catalyst - Wikipedia

    en.wikipedia.org/wiki/Wilkinson's_catalyst

    Wilkinson's catalyst (chlorido­tris(triphenylphosphine)­rhodium(I)) is a coordination complex of rhodium with the formula [RhCl(PPh 3) 3], where 'Ph' denotes a phenyl group. It is a red-brown colored solid that is soluble in hydrocarbon solvents such as benzene, and more so in tetrahydrofuran or chlorinated solvents such as dichloromethane .

  7. Phosphorus-31 nuclear magnetic resonance - Wikipedia

    en.wikipedia.org/wiki/Phosphorus-31_nuclear...

    The situation for phosphorus-carbon couplings are more complicated since the two-bond couplings are often larger than one-bond couplings. The J(13 C, 31 P) values for triphenylphosphine are respectively −12.5, 19.6, 6.8, and 0.3 for one-, two-, three-, and four-bond couplings. [4]

  8. Methylenetriphenylphosphorane - Wikipedia

    en.wikipedia.org/wiki/Methylenetriphenylphosphorane

    Solubility in water. decompose Solubility: THF Except where otherwise noted, ... The phosphorus-containing product is triphenylphosphine oxide. Structure

  9. Triphenyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Triphenyl_phosphite

    Solubility in water. low Solubility: organic solvents Magnetic susceptibility (χ)-183.7·10 −6 cm 3 /mol Hazards Occupational safety and health (OHS/OSH): Main ...