Category
page 1Homogeneous catalysis
hydrogenation
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Steps in the hydrogenation of a C=C double bond at a catalyst surface, for example Ni or Pt :
(1) The reactants are Adsorption|adsorbed on the catalyst surface and H2 dissociates.
(2) An H atom bonds to one C atom. The other C atom is still attached to the surface.
(3) A second C atom bonds to an H atom. The molecule leaves the surface.

hydroformylation
thumb|right|300px|Hydroformylation of an alkene (R to R [[organyl groups (i. e. alkyl- or aryl group) or hydrogen)]]
Wilkinson's catalyst
chemical compound
olefin metathesis
redistribution of olefinic (alkene) bonds
tetrakis(triphenylphosphine)palladium(0)
Tetrakis(triphenylphosphine)palladium(0) (sometimes called quatrotriphenylphosphine palladium) is the chemical compound [Pd(P(C6H5)3)4], often abbreviated Pd(PPh3)4, or rarely PdP4. It is a bright yellow crystalline solid that becomes brown upon decomposition in air.
Wacker process
chemical reaction
oil drying agent
painting implement
homogeneous catalysis
catalysis in a solution by a soluble catalyst
Crabtree's catalyst
complex of iridium
cyclooctadiene rhodium chloride dimer
chemical compound
tetrakis(triphenylphosphine)platinum(0)
Tetrakis(triphenylphosphine)platinum(0) is the chemical compound with the formula Pt(P(C6H5)3)4, often abbreviated Pt(PPh3)4. The bright yellow compound is used as a precursor to other platinum complexes.
hydrocyanation
In organic chemistry, hydrocyanation is a process for conversion of alkenes to nitriles. The reaction involves the addition of hydrogen cyanide and requires a catalyst if the substrate alkene is unactivated. This conversion is conducted on an industrial scale for the production of precursors to nylon. Direct hydrocyanation is rare in the laboratory because hydrogen cyanide is extremely toxic, but transfer variants can allow other nitrilic compounds to serve as hydrogen cyanide synthons.
bis(triphenylphosphine)platinum chloride
chemical compound
tris(triphenylphosphine)rhodium carbonyl hydride
chemical compound
rhodium carbonyl chloride
chemical compound
cyclooctadiene iridium chloride dimer
chemical compound
dichloro(1,5‐cyclooctadiene)palladium
Dichloro(1,5-cyclooctadiene)palladium is the organopalladium compound with the formula PdCl2(C8H12) where C8H12 is cycloocta-1,5-diene (cod) or abbreviated PdCl2(cod). It is a yellow solid that is soluble in chloroform. According to X-ray crystallography, the Pd center is square planar. This complex can be synthesized by reaction of tetrachloropalladate in hydrochloric acid with cycloocta-1,5-diene. A mechanochemical synthesis combines PdCl2 and cod.
Dicarbonyl(acetylacetonato)rhodium(I)
Dicarbonyl(acetylacetonato)rhodium(I) is an organorhodium compound with the formula Rh(O2C5H7)(CO)2. The compound consists of two CO ligands and an acetylacetonate. It is a dark green solid that dissolves in acetone and benzene, giving yellow solutions. The compound is used as a precursor to homogeneous catalysts.
Ethenolysis
In organic chemistry, ethenolysis is a chemical process in which internal olefins are degraded using ethylene () as the reagent. The reaction is an example of cross metathesis. The utility of the reaction is driven by the low cost of ethylene as a reagent and its selectivity. It produces compounds with terminal alkene functional groups (α-olefins), which are more amenable to other reactions such as polymerization and hydroformylation.
bis(1,5-cyclooctadiene)dimethoxydiiridium
chemical compound
1,1,3,3-tetramethyl-1,3-divinyldisiloxane
1,1,3,3-Tetramethyl-1,3-divinyldisiloxane (also referred to as tetramethyldivinyldisiloxane) is the organosilicon compound with the formula O(SiMe2CH=CH2)2.
chlorobis(cyclooctene)rhodium dimer
chemical compound