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Triphenylphosphine ph3p

Manufactured by Merck Group
Sourced in China

Triphenylphosphine (Ph3P) is a colorless, crystalline solid compound commonly used as a reagent in organic synthesis. It is a phosphine compound with the chemical formula C₁₈H₁₅P. Triphenylphosphine serves as a versatile ligand in coordination chemistry and is employed in various chemical reactions, including Wittig reactions, Mitsunobu reactions, and others.

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2 protocols using triphenylphosphine ph3p

1

Synthesis of Concentrated Hydrogen Peroxide

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A commercial aqueous solution of hydrogen peroxide (35 wt%, Fluka) was concentrated to 70 wt% by vacuum distillation at 45 °C/10 mm Hg (caution: risk of explosion. All glassware has to be thoroughly rinsed with distilled water to remove traces of any heavy metals). As the purity of commercial VO(acac)2 (Aldrich) is ca. 95%, it was dissolved in MeCN to obtain a saturated solution, which was then filtered through a micro-porous paper filter. The filtrate was evaporated at 40 °C under reduced pressure and the resulting solid was dried under vacuum at 20 °C for 48 h, leading to tiny dark-green (0.5–1.0 mm) crystals, which were used in the oxidation experiments. Cyclohexane, acetonitrile, triphenylphosphine (Ph3P), and tetra-n-butyl ammonium perchlorate (Aldrich) were analytical grade and used as received.
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2

Synthesis of Au Nanoparticles with Ligands

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The cupric (II) acetylacetonate (C10H14O4Cu), tetrachloroauric (III) acid (HAuCl4·3H2O, >99.99% metals basis), triphenylphosphine (Ph3P, ≥99%), tris(4-fluorophenyl)phosphine ((p-FPh)3P, ≥99%), NaBH4 (>98%) were received from Aldrich (Shanghai, China). Methanol, dichloromethane, and n-hexane were purchased from Aldrich (Shanghai, China). All reagents and solvents were commercially available and used without further purification. Pure water was purchased from Wahaha Co. Ltd. All glassware was thoroughly cleaned with aqua regia (HCl:HNO3 = 3:1, v-v), rinsed with copious pure water.
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