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  2. Tetrakis (triphenylphosphine)palladium (0) - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(triphenylphosphine...

    Tetrakis(triphenylphosphine)palladium(0) (sometimes called quatrotriphenylphosphine palladium) is the chemical compound [Pd(P(C 6 H 5) 3) 4], often abbreviated Pd(PPh 3) 4, or rarely PdP 4. It is a bright yellow crystalline solid that becomes brown upon decomposition in air .

  3. Solubility chart - Wikipedia

    en.wikipedia.org/wiki/Solubility_chart

    The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.

  4. Triphenylphosphine oxide - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine_oxide

    Triphenylphosphine oxide (often abbreviated TPPO) is the organophosphorus compound with the formula OP(C 6 H 5) 3, also written as Ph 3 PO or PPh 3 O (Ph = C 6 H 5).It is one of the more common phosphine oxides.

  5. Triphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine

    Triphenylphosphine undergoes slow oxidation by air to give triphenylphosphine oxide, Ph 3 PO: 2 PPh 3 + O 2 → 2 OPPh 3. This impurity can be removed by recrystallisation of PPh 3 from either hot ethanol or isopropanol. [8] This method capitalizes on the fact that OPPh 3 is more polar and hence more soluble in polar solvents than PPh 3.

  6. Palladium compounds - Wikipedia

    en.wikipedia.org/wiki/Palladium_compounds

    The catalytic ability is due to palladium's ability to switch between the Pd 0 and Pd 2+ oxidation states. An organic compound adds across Pd 0 to form an organic Pd 2+ complex (oxidative addition). After transmetalation with an organometallic compound, two organic ligands to Pd 2+ may exit the palladium complex and combine, forming a coupling ...

  7. Wilkinson's catalyst - Wikipedia

    en.wikipedia.org/wiki/Wilkinson's_catalyst

    [9] [10] [1] Triphenylphosphine serves as both a ligand and a two-electron reducing agent that oxidizes itself from oxidation state (III) to (V). In the synthesis, three equivalents of triphenylphosphine become ligands in the product, while the fourth reduces rhodium(III) to rhodium(I). RhCl 3 (H 2 O) 3 + 4 PPh 3 → RhCl(PPh 3) 3 + OPPh 3 + 2 ...

  8. Negishi coupling - Wikipedia

    en.wikipedia.org/wiki/Negishi_coupling

    Unlike palladium systems which involve only Pd 0 or Pd II, nickel catalyzed systems can involve nickel of different oxidation states. [17] Both systems are similar in that they involve similar elementary steps: oxidative addition, transmetalation, and reductive elimination.

  9. Triphenyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Triphenyl_phosphite

    ni(cod) 2 + 4 p(oc 6 h 5) 3 → ni[p(oc 6 h 5) 3] 4 + 2 cod Related complexes are homogeneous catalysts for the hydrocyanation of alkenes . It also forms a variety of Fe(0) and Fe(II) complexes such as the di hydride H 2 Fe[P(OC 6 H 5 ) 3 ] 4 .