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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. Tetrakis(triphenylphosphine)platinum(0) - Wikipedia

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

    The molecule is tetrahedral, with point group symmetry of T d, as expected for a four-coordinate metal complex of a metal with the d 10 configuration. [4] Even though this complex follows the 18 electron rule, it dissociates triphenylphosphine in solution to give the 16e − derivative containing only three PPh 3 ligands: Pt(PPh 3) 4 → Pt(PPh ...

  4. 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.

  5. 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 ...

  6. 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.

  7. 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]

  8. Oxidation state - Wikipedia

    en.wikipedia.org/wiki/Oxidation_state

    Fractional oxidation states are often used to represent the average oxidation state of several atoms of the same element in a structure. For example, the formula of magnetite is Fe 3 O 4, implying an average oxidation state for iron of + ⁠ 8 / 3 ⁠. [17]: 81–82 However, this average value may not be representative if the atoms are not ...

  9. Negishi coupling - Wikipedia

    en.wikipedia.org/wiki/Negishi_coupling

    [1] [2] A variety of nickel catalysts in either Ni 0 or Ni II oxidation state can be employed in Negishi cross couplings such as Ni(PPh 3) 4, Ni(acac) 2, Ni(COD) 2 etc. [3] [4] [5] The leaving group X is usually chloride, bromide, or iodide, but triflate and acetyloxy groups are feasible as well. X = Cl usually leads to slow reactions.