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  2. Palladium - Wikipedia

    en.wikipedia.org/wiki/Palladium

    Most palladium is used for catalytic converters in the automobile industry. [77] Catalytic converters are targets for thieves because they contain palladium and other rare metals. In the run up to year 2000, the Russian supply of palladium to the global market was repeatedly delayed and disrupted; for political reasons, the export quota was not ...

  3. Palladium compounds - Wikipedia

    en.wikipedia.org/wiki/Palladium_compounds

    Palladium forms a variety of ionic, coordination, and organopalladium compounds, typically with oxidation state Pd 0 or Pd 2+. Palladium(III) compounds have also been reported. Palladium compounds are frequently used as catalysts in cross-coupling reactions such as the Sonogashira coupling and Suzuki reaction.

  4. Organopalladium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organopalladium_chemistry

    Organopalladium chemistry is a branch of organometallic chemistry that deals with organic palladium compounds and their reactions. Palladium is often used as a catalyst in the reduction of alkenes and alkynes with hydrogen. This process involves the formation of a palladium-carbon covalent bond.

  5. Negishi coupling - Wikipedia

    en.wikipedia.org/wiki/Negishi_coupling

    In a novel modification palladium is first oxidized by the haloketone 2-chloro-2-phenylacetophenone 1 and the resulting palladium OPdCl complex then accepts both the organozinc compound 2 and the organotin compound 3 in a double transmetalation: [25] Examples of nickel catalyzed Negishi couplings include sp 2-sp 2, sp 2-sp 3, and sp 3-sp 3 systems.

  6. Suzuki reaction - Wikipedia

    en.wikipedia.org/wiki/Suzuki_reaction

    The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. [1] [2] [3] It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their contribution to the discovery and development of noble metal catalysis in organic ...

  7. Heck reaction - Wikipedia

    en.wikipedia.org/wiki/Heck_reaction

    This reaction was the first example of a carbon-carbon bond-forming reaction that followed a Pd(0)/Pd(II) catalytic cycle, the same catalytic cycle that is seen in other Pd(0)-catalyzed cross-coupling reactions. The Heck reaction is a way to substitute alkenes.

  8. Wacker process - Wikipedia

    en.wikipedia.org/wiki/Wacker_process

    The construction of a new oil refinery in Cologne by Esso close to a Wacker site, combined with the realization that ethylene would be a cheaper feedstock prompted Wacker to investigate its potential uses. As part of the ensuing research effort, a reaction of ethylene and oxygen over palladium on carbon in a quest for ethylene oxide ...

  9. Palladium on carbon - Wikipedia

    en.wikipedia.org/wiki/Palladium_on_carbon

    Palladium on carbon, often referred to as Pd/C, is a form of palladium used as a catalyst. [1] The metal is supported on activated carbon to maximize its surface area and activity . Uses