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  2. Olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Olefin_metathesis

    In organic chemistry, olefin metathesis is an organic reaction that entails the redistribution of fragments of alkenes (olefins) by the scission and regeneration of carbon-carbon double bonds. [ 1 ] [ 2 ] Because of the relative simplicity of olefin metathesis, it often creates fewer undesired by-products and hazardous wastes than alternative ...

  3. Shell higher olefin process - Wikipedia

    en.wikipedia.org/wiki/Shell_higher_olefin_process

    The first step in this process is the ethylene oligomerization to a mixture of even-numbered α-olefins at 80 to 120 °C and 70 to 140 bar (7 to 14 MPa) catalyzed by a nickel-phosphine complex. Such catalysts are typically prepared from diarylphosphino carboxylic acids, such as (C 6 H 5 ) 2 PCH 2 CO 2 H. [ 5 ] The process and its mechanism was ...

  4. Carbonyl olefin metathesis - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_olefin_metathesis

    The metal-mediated processes include a carbonyl-olefination and an olefinolefin metathesis event. There are two general mechanistic schemes to perform this overall transformation: one, reaction of a [M=CHR 1] reagent with an alkene to generate a new metal alkylidene, which then couples with a carbonyl group to form the desired substituted alkene and an inactive [M=O] species (type A); two ...

  5. Ring-opening metathesis polymerisation - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_metathesis...

    The mechanism of homogeneous ring-opening metathesis polymerization is well-studied. It is similar to any olefin metathesis reaction. Initiation occurs by forming an open coordination site on the catalyst. Propagation happens via a metallacycle intermediate formed after a 2+2 cycloaddition. When using a G3 catalyst, 2+2 cycloaddition is the ...

  6. Ring-closing metathesis - Wikipedia

    en.wikipedia.org/wiki/Ring-closing_metathesis

    Ring-closing metathesis (RCM) is a widely used variation of olefin metathesis in organic chemistry for the synthesis of various unsaturated rings via the intramolecular metathesis of two terminal alkenes, which forms the cycloalkene as the E-or Z-isomers and volatile ethylene.

  7. Straight-chain terminal alkene - Wikipedia

    en.wikipedia.org/wiki/Straight-chain_terminal_alkene

    The Gulf linear alpha olefin process is commonly called a catalytic Ziegler process. Triethyl aluminium is used as a catalyst, but in catalytic amounts the process is a single-step process. Tri-ethyl aluminium and excess ethylene are fed to a plug flow-reactor. The reaction is conducted at high pressure and high temperature.

  8. Ring-opening polymerization - Wikipedia

    en.wikipedia.org/wiki/Ring-opening_polymerization

    The mechanism for ROMP follows similar pathways as olefin metathesis. The initiation process involves the coordination of the cycloalkene monomer to the metal alkylidene complex, followed by a [2+2] type cycloaddition to form the metallacyclobutane intermediate that cycloreverts to form a new alkylidene species. [23] [24]

  9. Rearrangement reaction - Wikipedia

    en.wikipedia.org/wiki/Rearrangement_reaction

    Olefin metathesis is a formal exchange of the alkylidene fragments in two alkenes. It is a catalytic reaction with carbene , or more accurately, transition metal carbene complex intermediates. In this example ( ethenolysis , a pair of vinyl compounds form a new symmetrical alkene with expulsion of ethylene .