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  2. 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)], 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 .

  3. Tsuji–Wilkinson decarbonylation reaction - Wikipedia

    en.wikipedia.org/wiki/Tsuji–Wilkinson...

    The Tsuji–Wilkinson decarbonylation reaction is a method for the decarbonylation of aldehydes and some acyl chlorides. The reaction name recognizes Jirō Tsuji, whose team first reported the use of Wilkinson's catalyst (RhCl(PPh 3) 3) for these reactions: RC(O)X + RhCl(PPh 3) 3 → RX + RhCl(CO)(PPh 3) 2 + PPh 3

  4. Hydroacylation - Wikipedia

    en.wikipedia.org/wiki/Hydroacylation

    The reaction required tin tetrachloride and a stoichiometric amount of Wilkinson's catalyst: An equal amount of a cyclopropane was formed as the result of decarbonylation. The first catalytic application involved cyclization of 4-pentenal to cyclopentanone using (again) Wilkinson's catalyst. [4] In this reaction the solvent was saturated with ...

  5. Photooxygenation - Wikipedia

    en.wikipedia.org/wiki/Photooxygenation

    A photooxygenation is a light-induced oxidation reaction in which molecular oxygen is incorporated into the product(s). [1] [2] Initial research interest in photooxygenation reactions arose from Oscar Raab's observations in 1900 that the combination of light, oxygen and photosensitizers is highly toxic to cells. [3]

  6. Catalysis - Wikipedia

    en.wikipedia.org/wiki/Catalysis

    The catalyst may increase the reaction rate or selectivity, or enable the reaction at lower temperatures. This effect can be illustrated with an energy profile diagram. In the catalyzed elementary reaction, catalysts do not change the extent of a reaction: they have no effect on the chemical equilibrium of a reaction.

  7. Photocatalysis - Wikipedia

    en.wikipedia.org/wiki/Photocatalysis

    2 catalyst combined with an Au light absorber accelerated hydrogen sulfide-to-hydrogen reactions. The process is an alternative to the conventional Claus process that operates at 800–1,000 °C (1,470–1,830 °F). [29] A Fe catalyst combined with a Cu light absorber can produce hydrogen from ammonia (NH 3) at ambient temperature using visible ...

  8. Light-dependent reactions - Wikipedia

    en.wikipedia.org/wiki/Light-dependent_reactions

    To do this, it must release the absorbed energy. This can happen in various ways. The extra energy can be converted into molecular motion and lost as heat, or re-emitted by the electron as light (fluorescence). The energy, but not the electron itself, may be passed onto another molecule; this is called resonance energy transfer.

  9. Photoredox catalysis - Wikipedia

    en.wikipedia.org/wiki/Photoredox_catalysis

    In fact, the concentration of excited-state species in the cell should change exactly in phase with the intensity of light incident on the electrochemical cell. If the potential applied to the cell is strong enough for electron transfer to occur, the change in concentration of the redox-competent excited state can be measured as an alternating ...

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