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Perfluoro-1,3-butadiene, dimerization

Irradiation of the anti-dimer of perfluorotetramethylcyclobutadiene in a fluorocarbon solvent affords a mixture of perfluoro-octamethylcubane and perfluoro-octamethylcuneane the intermediacy of the butadiene syn-dimer and of perfluoro-octamethylcyclo-octatetraene is proposed. Hydrogenolysis of the 4-substituted homocubanes (752 X = Br, Y = Cl, Br, COjH, CH2OH, or COjMe) over various... [Pg.352]

At 200°C, perfluoro-1,3-butadiene dimerizes. What is the structure of the dimer ... [Pg.33]

Cycloadditions of fluorinated dienes are known to give cyclobutane rings. The original suggestion of the structure of the dimer of perfluoro-1,3-butadiene was perfluorotricyclo[4,2,0,02 5]octane [727]. The compound did not react with potassium permanganate. Fifteen years later, another formula was found correct based on physical methods. Instead of three four-membered rings, the product consists of three five-membered rings. Its name is perfluorotricyclo[3,3,0,02 6]octane [128],... [Pg.105]


See other pages where Perfluoro-1,3-butadiene, dimerization is mentioned: [Pg.97]    [Pg.431]    [Pg.33]    [Pg.389]   
See also in sourсe #XX -- [ Pg.33 , Pg.105 ]




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Dimerization butadiene

Perfluoro-1,3-butadiene

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