organopalladium

organopalladium
Describing any organic compound containing a carbon to palladium bond

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  • 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 …   Wikipedia

  • Organometallic chemistry — n Butyllithium, an organometallic compound. Four lithium atoms are shown in purple in a tetrahedron, and each lithium atom is bound to a butyl group (carbon is black, hydrogen is white). Organometallic chemistry is the study of chemical compounds …   Wikipedia

  • Heck reaction — The Heck reaction (also called the Mizoroki Heck reaction)[1] is the chemical reaction of an unsaturated halide (or triflate) with an alkene and a base and palladium catalyst to form a substituted alkene.[2][3] Together with the other palladium… …   Wikipedia

  • Wacker process — The Wacker process or the Hoechst Wacker process (named after the chemical companies of the same name) originally referred to the oxidation of ethylene to acetaldehyde by oxygen in water in the presence of a tetrachloropalladate catalyst.… …   Wikipedia

  • Compuesto de organopaladio — Un compuesto de organopaladio es un compuesto químico orgánico que contiene átomos de carbono y de paladio, unidos por enlaces químicos. La química Organopaladio es una rama de la química organometálica que se ocupa de los compuestos orgánicos de …   Wikipedia Español

  • Gel — For other uses, see Gel (disambiguation). An upturned vial of hair gel A gel (from the lat. gelu freezing, cold, ice or gelatus frozen, immobile) is a solid, jelly like material that can have properties ranging from soft and weak to hard and… …   Wikipedia

  • Suzuki reaction — The Suzuki reaction is the organic reaction of an aryl or vinyl boronic acid with an aryl or vinyl halide catalyzed by a palladium(0) complex. [Miyaura, N. et al. Tetrahedron Lett. 1979, 3437.] [Miyaura, N.; Suzuki, A. Chem. Commun. 1979, 866.]… …   Wikipedia

  • Sonogashira coupling — In organic chemistry, a Sonogashira coupling is a coupling reaction of terminal alkynes with aryl or vinyl halides. This reaction was first reported by Kenkichi Sonogashira and Nobue Hagihara in 1975. [cite journal author = K. Sonogashira, Y.… …   Wikipedia

  • Coupling reaction — A coupling reaction in organic chemistry is a catch all term for a variety of reactions where two hydrocarbon fragments are coupled with the aid of a metal catalyst. In one important reaction type a main group organometallic compound of the type… …   Wikipedia

  • Organoborane — PropertiesThe C B bond has low polarity (the difference in electronegativity 2.55 for carbon and 2.04 for boron) and therefore alkyl boron compounds are in general stable though easily oxidized. Vinyl groups and aryl groups donate electrons and… …   Wikipedia

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