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  2. Palladium - Wikipedia

    en.wikipedia.org/wiki/Palladium

    The largest use of palladium today is in catalytic converters. [41] Palladium is also used in jewelry, dentistry, [41] [42] watch making, blood sugar test strips, aircraft spark plugs, surgical instruments, and electrical contacts. [43] Palladium is also used to make some professional transverse (concert or classical) flutes. [44]

  3. 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.

  4. 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.

  5. Noble metal - Wikipedia

    en.wikipedia.org/wiki/Noble_metal

    While lists of noble metals can differ, they tend to cluster around gold and the six platinum group metals: ruthenium, rhodium, palladium, osmium, iridium, and platinum. In addition to this term's function as a compound noun, there are circumstances where noble is used as an adjective for the noun metal.

  6. Stille reaction - Wikipedia

    en.wikipedia.org/wiki/Stille_reaction

    The mechanism of the Stille reaction has been extensively studied. [11] [23] The catalytic cycle involves an oxidative addition of a halide or pseudohalide (2) to a palladium catalyst (1), transmetalation of 3 with an organotin reagent (4), and reductive elimination of 5 to yield the coupled product (7) and the regenerated palladium catalyst (1).

  7. 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 ...

  8. 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 ...

  9. 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 ...