Utilizing the regioselectivity of perfluoropyridine towards the preparation of phenyoxyacetylene precursors for partially fluorinated polymers of diverse architecture was written by Corley, Cynthia A.;Kobra, Khadijatul;Peloquin, Andrew J.;Salmon, Katelynn;Gumireddy, Lionel;Knoerzer, Timm A.;McMillen, Colin D.;Pennington, William T.;Schoffstall, Allen M.;Iacono, Scott T.. And the article was included in Journal of Fluorine Chemistry in 2019.COA of Formula: C5F5N The following contents are mentioned in the article:
Regioselective nucleophilic substitution of perfluoropyridine with functionalized phenols provided a facile route toward the preparation of 2,6-bis(4-ethynylphenoxy)-3,5-difluoro-4-phenoxypyridine, a monomer that can be polymerized neat via thermal [2 + 2 + 2] cyclopolymns. affording intractable polyarylene networks or via copper-assisted step-growth 1,3-dipolar alkyne-azide “click” cycloaddition reactions with bis(azidomethyl)benzene. Both reactive pathways afforded polymers with high thermal stability and good char yields, which is comparable to acetylene-based resins. Notably, the opportunity for programmable thermal properties is realized through the operationally simple monomer synthesis was shown to be adaptive to various regioselective and nucleophile addition scenarios that can lead to the production of a library of perfluoropyridine monomers. Herein, we highlight the synthesis and characterization of these new perfluoropyridine-based polymer architectures for potentially tunable high performance applications. This study involved multiple reactions and reactants, such as 2,3,4,5,6-Perfluoropyridine (cas: 700-16-3COA of Formula: C5F5N).
2,3,4,5,6-Perfluoropyridine (cas: 700-16-3) belongs to pyridine derivatives. In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. Pyridine, its benzo and pyridine-based compounds play diverse roles in organic chemistry. Pyridine-based materials are valued for their optical and physical properties as well as their medical potential. COA of Formula: C5F5N