AROMATIC SIMPLE POLYESTERS OF TRYPTICENDIOL-2,5
https://doi.org/10.31143/2221-7789-2023-2-80-87
EDN: FZXGAV
Abstract
The synthesis and properties of polyarylene oxides, aromatic polyesters based on trypticendiol-2,5, are considered. It has been shown that polyarylene oxides of trypticendiol-2,5 have higher characteristics compared to the prop- erties of similar polymers based on the common bisphenol A. It has been established that polyarylene oxides of trypticendiol-2,5 have a number of specific properties important from a practical point of view related to the unique structure of trypticene.
About the Authors
K. B. Temiraev
North Caucasian Institute of Mining and Metallurgy (State Technological University)
Russian Federation
Russian Federation
M. V. Khudoyan
North Caucasian Institute of Mining and Metallurgy (State Technological University)
Russian Federation
Russian Federation
I. V. Mishenina
North Caucasian Institute of Mining and Metallurgy (State Technological University)
Russian Federation
Russian Federation
G. B. Shustov
Kabardino-Balkarian State University
Russian Federation
Russian Federation
S. M. Balaeva
Kabardino-Balkarian State University
Russian Federation
Russian Federation
R. A. Shetov
Kabardino-Balkarian State University
Russian Federation
Russian Federation
References
1. Коршак В.В. Термостойкие полимеры. М.: Наука, 1969. 411 с.
2. Коршак В.В. Химическое строение и температурные характеристики полимеров. М.: Наука, 1970. 390
3. с.
4. Hay A.S. Aromatic polyethers // Adv. Polym. Sci. 1967. N 4. P. 496.
5. Maiti S., Mandal B. Aromatic polyethers by nucleophilic displacement polymerization // Prog. Polym. Sci.
6. P. 111.
7. Rose J.B. High Performance Polymers: Their Origin and Development / Ed. by R.B. Seymour,
8. G.S. Kirschenbaum. New York: Elsevier, 1986. 187 p.
9. Labadie J.W., Hedrick J.L., Ueda M. // Step-Growth Polymers for High Performance Materials / Ed. by J.L. Hedrick, J.W. Labadie. ACS Washington: ACS Symp. Ser. 624. 1996. 210 p.
10. Mullins M.J., Woo E.P. The synthesis and properties of poly (aromatic ketones) // J. Macromol. Sci. Rev., Macromol. Chem. Phys. 1987. V. 27, N 2. P. 313.
11. Rao V.L. Polyether ketones // J. Macromol. Sci. Rev., Macromol. Chem. Phys. 1995. V. 35, N 4. P. 661.
12. Rao V L. Polyether sulfones // J. Macromol. Sci. Rev., Macromol. Chem. Phys. 1999. V. 39, N 4. P. 655.
13. Rose J.B. Recent Advances in Mechanistic and Synthetic Aspects of Polymerization / Ed. by
14. M. Fontanille, A. Guyot. Oxford: Pergamon, 1989. 413 p.
15. Takekoshi T. Synthesis of high performance aromatic polymers via nucleophilic nitro displacement reaction
16. // Polym. J. 1987. V. 19, N 1. P. 191.
17. Русанов А.Л., Takekoshi T. Реакции синтеза ароматических полимеров с использованием нитросодержащих мономеров // Успехи химии. 1991. Т. 60, № 7. С. 1449.
18. Русанов А.Л., Беломоина Н.М. Тепло- и термосойкие ароматические полиэфиры на основе гетероциклических бисфенолов // Высокомолек. соедин. C. 2009. Т. 51, № 7. С. 1346–1385.
19. Bartlett P.D., Ryan M.J., Cohen S.G. Triptycene (9,10-o-benzenoanthracene) // J. Amer. Chem. Soc. 1942.
20. V. 64. P. 2649–2653.
21. Boyles D.A., Filipova T.S., Bendler J.T. Aromatic copolycarbonates of bisphenol A and triptycene-1,4- hydroquinone // Polymer Preprints. 2007. V. 48, N 1. P. 352–353.
22. Kasashima Y., Kaneda T., Akutsu F., Naruchi K., Miura M. Synthesis and properties of aromatic polyamides and polyimides from 9,10-dihydro-9,10-o-benzenoanthracene-1,4-diamine // Polymer J. 1994.
23. V. 26, N 10. P. 1179.
24. Sydlik S.A., Zhihua Chen, Swager T.M. Triptycene polyimides: soluble polymers with high thermal stability and low refractive indices // Macromolecules. 2011. V. 44, N 4. P. 976.
25. Pat. DE № 4121138 A1. Polyarylene ethers with high glass transition pt. and good melt process abilitycontain units derived from aromatic dihalides, triptycene bisphenol and opt. other dihydric phenols / Wilharm P. Publ. date 26.06.1993.
26. La Shonda Tanika Cureton. Modified poly (arylene ether sulfone) compositions and their segmented block copolymers. PhD in Chemistry Dissertation. Blacksburg, 2010. 117 p.
27. Rifai S., Breen, C.A., Solis D.J., Swager T.M. Facile in situ silver nanoparticle formation in insulating porous polymer matrices // Chemistry of Materials. 2006. N 18. P. 21.
28. Koo W.-T., Kim Y., Kim S., Suh B.L., Savagatrup S., Kim J., Lee S.-J., Swager T.M., Kim J.D. Hydrogen sensors from composites of ultrasmall bimetallic nanoparticles and porous ion-exchange polymers // Chem. 2020. V. 6, N
29. P. 2746–2758.
30. Goods J.B. Design and synthesis of functional graphenic and triptycene poly(arylether) materials. Dissertation submitted to the Department of Chemistry In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy at the Massachusetts institute of technology. Massachusetts, 2015. 215 p.
31. Johnson R.N., Farnham A.G., Clendinning R.A., Hale W.F., Merriam C.N. Poly (aryl ethers) by nucleophilic aromatic substitution. I. Synthesis and properties // J. Polym. Sci. A-1. 1967. V. 5, N 9. P. 2375.
32. Русанов А.Л., Саркисян Г.Б., Кештов М.Л. Полиариленоксиды на основе новых типов, активированных дифторароматических соединений // Высокомолек. соедин. А. 1999. Т. 41, № 1. С. 27.
33. Long T.M., Swager T.M. Molecular design of free volume as a route to low-k dielectric materials //
34. J. Amer. Chem. Soc. 2003. V. 125, N 46. Р. 14113.
35. Schulz B., Bruma M., Brehmer L. Aromatic poly(1,3,4-oxadiazole) s as advanced materials // Adv. Mater. 1997. V. 9, N 8. Р. 601.
36. Gong F., Mao H., Zhang Y., Zhang S., Xing W. Synthesis of highly sulfonated poly (arylene ether sulfone) s with sulfonated triptycene pendants for proton exchange membranes // Polymer. 2011. V. 52. P. 1738.
37. Rikukawa M., Sanui K. Proton-conducting polymer electrolyte membranes bazed on hydrocarbon polymers
38. // Progr. Polym. Sci. 2000. V. 25. P. 1463.
39. Brandon N.P., Skinner S., Steele B. Recent advances in materials for fuell cells // Annu. Rev. Mater. Res. 2003. V. 33. P. 183.
40. Shoesmith J.P., Collins R.D., Oakley M.J., Stevenson D.K. Status of solid polymer fuell cell system development // J. Power Sours. 1994. V. 49. P. 129.
41. Carrette I., Friedrich K.A., Stimming U. Fuell cells-fundamental and applications // Chem. Phys. Chem. 2000. N 4. P. 162.
42. Yang J.S., Yan J.L. Central-ring functionalization and application of the rigid aromatic, and H-shaped pentiptycene scaffold // Chem. Commun. 2008. N 13. P. 1501.
43. Swager T.M. Iptycenes in the design of high performance polymers // Acc. Chem. Res. 2008.
44. V. 41. P. 1181.
45. Патент РФ № 2467031. Полигидроксиэфиры на основе триптицендиола-2,5 / Беева Д.А., Микитаев А.К., Беев А.А. Опубликовано 20.11.2012 г.
46. А.с. СССР № 01180367. Галоидпроизводные на основе триптицендиола-2,5 для получения поликонденсационных полимеров / Микитаев А.К., Сердюк О.А., Прядко В.Н. Опубликовано 23.09.1985 г.
47. Микитаев А.К., Коршак В.В., Гурдалиев Х.Х. Новые полиарилаты на основе триптицендиола-2,5 // Докл. АН СССР. 1983. Т. 269, № 1. С. 127–12
Review
For citations:
Temiraev K.B., Khudoyan M.V., Mishenina I.V., Shustov G.B., Balaeva S.M., Shetov R.A. AROMATIC SIMPLE POLYESTERS OF TRYPTICENDIOL-2,5. Proceedings of the Kabardino-Balkarian State University. 2023;13(2):80-87. (In Russ.) https://doi.org/10.31143/2221-7789-2023-2-80-87. EDN: FZXGAV
Views:
33
JATS XML
Email this article 