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  2. Metal carbonyl - Wikipedia

    en.wikipedia.org/wiki/Metal_carbonyl

    Another important reaction catalyzed by metal carbonyls is the hydrocarboxylation. The example below is for the synthesis of acrylic acid and acrylic acid esters: Also the cyclization of acetylene to cyclooctatetraene uses metal carbonyl catalysts: [61]

  3. Metal carbonyl hydride - Wikipedia

    en.wikipedia.org/wiki/Metal_carbonyl_hydride

    Metal carbonyl hydrides are used as catalysts in the hydroformylation of olefins. The catalyst is usually formed in situ in a reaction of a metal salt precursor with the syngas . The hydroformylation starts with the generation of a coordinatively unsaturated 16-electron metal carbonyl hydride complex like HCo(CO) 3 or HRh(CO)(PPh 3 ) 2 by ...

  4. Carbonylation - Wikipedia

    en.wikipedia.org/wiki/Carbonylation

    Metal carbonyls, compounds with the formula M(CO) x L y (M = metal; L = other ligands) are prepared by carbonylation of transition metals. Iron and nickel powder react directly with CO to give Fe(CO) 5 and Ni(CO) 4, respectively. Most other metals form carbonyls less directly, such as from their oxides or halides.

  5. Dicobalt octacarbonyl - Wikipedia

    en.wikipedia.org/wiki/Dicobalt_octacarbonyl

    Dicobalt octacarbonyl is an organocobalt compound with composition Co 2 (CO) 8.This metal carbonyl is used as a reagent and catalyst in organometallic chemistry and organic synthesis, and is central to much known organocobalt chemistry.

  6. Migratory insertion - Wikipedia

    en.wikipedia.org/wiki/Migratory_insertion

    Oxidation state – Oxidation of the metal tends to increase insertion reaction rates. The main rate-limiting step in the mechanism is the migration of the methyl group onto a carbonyl ligand, oxidizing the metal by imparting a greater partial positive charge on the acetyl carbon, and thus increasing the rate of reaction. [7]

  7. Carbonyl group - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_group

    In organic chemistry, a carbonyl group is a functional group with the formula C=O, composed of a carbon atom double-bonded to an oxygen atom, and it is divalent at the C atom. It is common to several classes of organic compounds (such as aldehydes , ketones and carboxylic acid ), as part of many larger functional groups.

  8. Pauson–Khand reaction - Wikipedia

    en.wikipedia.org/wiki/Pauson–Khand_reaction

    The Pauson–Khand (PK) reaction is a chemical reaction, described as a cycloaddition.In it, an alkyne, an alkene, and carbon monoxide combine into a α,β-cyclopentenone in the presence of a metal-carbonyl catalyst [1] [2] Ihsan Ullah Khand (1935–1980) discovered the reaction around 1970, while working as a postdoctoral associate with Peter Ludwig Pauson (1925–2013) at the University of ...

  9. Insertion reaction - Wikipedia

    en.wikipedia.org/wiki/Insertion_reaction

    The insertion of carbon monoxide and alkenes into metal-carbon bonds is a widely exploited reaction with major industrial applications. [21] [22]Nucleophilic insertion and rearrangement of a square planar complex