Perfluoroalkyl- and perfluoroalkylether-substituted quinoxalines
A series of perfluoroalkyl-and perfluoroalkylether-substituted quinoxalines was synthesized to determine the effect of the attachment of the perfluorinated unit to the heterocyclic ring (directly or via a phenyl group) and the effect of the nature of the perfluoroalkylether chain on the thermal and oxidative stability. Both model compounds and polymeric materials were investigated. Quinoxalines wherein the heterocyclic rings were bridged by polyperfluoroalkylethers with either two or three CF2 groups separating the ether oxygen from the heterocyclic ring were thermally stable below 316 °C. A polyquinoxaline system linked by a p-C6H4(CF2)3O(CF2)4O(CF2)4O(CF2)3-p-C6H4 chain exhibited thermal and thermal oxidative stability above 330 °C. Having two CF2 groups separating the aromatic ring from the ether oxygen led to a significantly lower stability and difficulties in the intermediate tetraketone synthesis.
Paciorek,Masuda,Lin,Nakahara
p. 27 - 38
(2007/10/03)
FLUORO-KETONES VI. SYNTHESIS OF PERFLUORO DI- AND TETRA-KETONES FROM 1,1-DICHLOROBENZYLLITHIUM AND PERFLUOROESTERS
The reaction of C6H5CCl2Li with perfluorinated mono and diesters yields fluorochloroketones in high yield.Hydrolysis of such compounds produces alpha-beta fluorinated di- and tetra-ketones, respectively.Various hydrates of the fluorinated ketones have bee
Chen, Loomis S.,Tamborski, Christ
p. 269 - 280
(2007/10/02)
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