stereospecific catalyst

stereospecific catalyst
a catalyst that preferentially catalyses the formation of one of a pair of stereoisomers, or one of a set of stereoisomeric polymers

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  • stereospecific — ster•e•o•spe•cif•ic [[t]ˌstɛr i oʊ spəˈsɪf ɪk, ˌstɪər [/t]] adj. 1) chem. producing or restricted to a specific stereoisomer: a stereospecific catalyst[/ex] 2) chem. stereoregular • Etymology: 1945–50 ster e•o•spec i•fic′i•ty ˌspɛs əˈfɪs ɪ ti n …   From formal English to slang

  • Ziegler–Natta catalyst — A Ziegler–Natta catalyst is a catalyst used in the synthesis of polymers of 1 alkenes (α olefins). Three types of Ziegler–Natta catalysts are currently employed: Solid and supported catalysts based on titanium compounds. They are used in… …   Wikipedia

  • Ziegler-Natta catalyst — A Ziegler Natta catalyst is a reagent or a mixture of reagents used in the production of polymers of 1 alkenes (α olefins). Ziegler Natta catalysts are typically based on titanium compounds and organometallic aluminium compounds, for example… …   Wikipedia

  • Ziegler catalyst — /ˈziglə kætələst/ (say zeegluh katuhluhst) noun a catalyst which promotes the polymerisation of ethylene and propylene at normal temperatures and pressures, as titanium trichloride; used in the production of stereospecific polymers. {named after… …  

  • reaction mechanism — Introduction       in chemical reactions (chemical reaction), the detailed processes by which chemical substances are transformed into other substances. The reactions themselves may involve the interactions of atoms (atom), molecules (molecule),… …   Universalium

  • Olefin metathesis — or transalkylidenation is an organic reaction that entails redistribution of alkylene fragments by the scission of carbon carbon double bonds in olefins (alkenes).[1] Its advantages include the creation of fewer sideproducts and hazardous wastes …   Wikipedia

  • Chemical reaction — Chemical reactions redirects here. For the 2007 television episode, see Chemical Reactions (Men in Trees). A thermite reaction using iron(III) oxide. The sparks …   Wikipedia

  • Oxaziridine — Oxaziridine …   Wikipedia

  • asymmetric synthesis — Chemical reaction by which unequal amounts of two product isomers are formed. It is normally not possible to synthesize from materials that do not have optical activity (i.e., are not chiral) one stereoisomer of a chiral compound without the… …   Universalium

  • Aldol reaction — The aldol reaction is a powerful means of forming carbon–carbon bonds in organic chemistry.[1][2][3] Discovered independently by …   Wikipedia

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