Synthesis of 4,4′-bis(nonafluorobiphenyl-4-oxyphenyl)-bis(trifluoromethyl)methane and a ladder polyether with spirobisindane fragments on its base
DOI:
https://doi.org/10.15407/dopovidi2015.07.116Keywords:
fluorinated monomers, fluorinated poly(arylene ether)s, ladder polymers, PIM polymers, trifluoromethyl groupsAbstract
A method of synthesis of 4,4′-bis(nonafluorobiphenyl-4-oxyphenyl)-containing monomer with 1,1,1,3,3,3-hexafluoropropane fragment based on decafluorobiphenyl and 4,4′-(hexafluoroisopropylidene)diphenol is developed. Ladder-type fluorinated aromatic polyether having both perfluorinated aromatic units and CF3-groups, as well as both rigid dibenzodioxin and spirobisindane fragments, is synthesized by the interaction of the obtained monomer with 5,5′,6,6′-tetrahydroxy-3,3,3′ ,3′-tetramethyl-1,1′-spirobisindane. The structures of the prepared monomer and the polymer were determined using 1H, 19F NMR and IR spectroscopy techniques. It is shown that the synthesized polyether has high glass transition temperature and good thermooxidative stability.
Downloads
References
Shevchenko V.V., Tkachenko I.M., Shekera O.V. Polym. Sci., Ser. B., 2010, 52, No 7–8: 408–430. https://doi.org/10.1134/S1560090410070055
Dhara M.G., Banerjee S. Prog. Polym. Sci., 2010, 35, No 8: 1022–1077. https://doi.org/10.1016/j.progpolymsci.2010.04.003
Ghosh A., Banerjee S. e-Polymers., 2014, 14, No 4: 227–257.
Maier G. Prog. Polym. Sci., 2001, 26, No 1: 3–65. https://doi.org/10.1016/S0079-6700(00)00043-5
McKeown N.B. ISRN Mater. Sci., 2012, 2012, Article ID 513986: 1–16.
Budd P.M., Bader S.G., Makhseed S., McKeown N.B., Msayib K. J., Tattershall C. E. Chem. Commun., 2004, No 2: 230–231. https://doi.org/10.1039/b311764b
Budd P.M., Makhseed S.M., Ghanem B. S., Msayib K. J., Tattershall C. E., McKeown N.B. Mater. Today, 2004, 7, No 4: 40–46. https://doi.org/10.1016/S1369-7021(04)00188-9
Carta M., Msayib K. J., Budd P.M., McKeown N.B. Org. Lett., 2008, 10, No 13: 2641–2643. https://doi.org/10.1021/ol800573m
Cui Z., Drioli E., Lee Y.M. Prog. Polym. Sci., 2014, 39, No 1: 164–198. https://doi.org/10.1016/j.progpolymsci.2013.07.008
Yampolskii Y. Macromolecules, 2012, 45, No 8: 3298–3311. https://doi.org/10.1021/ma300213b
Du N., Robertson G. P., Song J., Pinnau I., Thomas S., Guiver M.D. Macromolecules, 2008, 41, No 24: 9656–9662. https://doi.org/10.1021/ma801858d
Makhseed S., Samuel J., Bumajdad A., Hassan M. J. Appl. Polym. Sci., 2008, 109, No 4: 2591–2597. https://doi.org/10.1002/app.28372
Song J., Du N., Dai Y., Robertson G.P., Guiver M.D., Thomas S., Pinnau I. Macromolecules, 2008, 41, No 20: 7411–7417. https://doi.org/10.1021/ma801000u
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2025 Reports of the National Academy of Sciences of Ukraine

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.