{"id":1889,"date":"2018-01-10T16:26:05","date_gmt":"2018-01-10T13:26:05","guid":{"rendered":"http:\/\/polymerjournal.kiev.ua\/en\/?page_id=1889"},"modified":"2018-02-14T17:55:38","modified_gmt":"2018-02-14T14:55:38","slug":"2015-2-9","status":"publish","type":"page","link":"http:\/\/polymerjournal.kiev.ua\/en\/2015-2-9\/","title":{"rendered":"2015 (2) 9"},"content":{"rendered":"<p><a href=\"https:\/\/doi.org\/10.15407\/polymerj.37.02.168\">https:\/\/doi.org\/10.15407\/polymerj.37.02.168<\/a><\/p>\n<p><strong>Synthesis of allyl-containing poly(arylene ether)s copolymers with mono- and biphenylene fragments in main chain<\/strong><\/p>\n<p><strong><em>\u00a0<\/em><\/strong><\/p>\n<p><strong><em>\u0406<\/em><\/strong><strong><em>.<\/em><\/strong><strong><em>\u041c<\/em><\/strong><strong><em>. Tkachenko, A.V. Sidorenko, <\/em><\/strong><strong><em>\u041e<\/em><\/strong><strong><em>.V. Shekera, V.V. Shevchenko<\/em><\/strong><\/p>\n<p>&nbsp;<\/p>\n<p>Institute of Macromolecular Chemistry NAS of Ukraine<\/p>\n<p>48, Kharkivske shose, Kyiv, 02160, Ukraine<\/p>\n<p>&nbsp;<\/p>\n<p>Polym. J., 2015, <strong>37<\/strong>, no. 2: 168-173.<\/p>\n<p>&nbsp;<\/p>\n<p>Section: Synthesis polymers.<\/p>\n<p>&nbsp;<\/p>\n<p>Language: Russian.<\/p>\n<p>&nbsp;<\/p>\n<p>Abstract:<\/p>\n<p><em>Methods of synthesis of allyl-containing core-fluorinated poly(arylene ether)s copolymers with tetrafluorobenzene and octafluorobiphenylene units and 2-allylbenzene and nonfluorinated meta-phenylenoxide fragments were developed. The polyethers were prepared from ternary copolycondensation of three core-fluorinated components, namely by interaction of decafluorobiphenyl with 2-(prop-2-en-1-yl)-4-{2,3,5,6-tetra<\/em><em>\u044b<\/em><em>uoro-4-[4-hydroxy-3-(prop-2-en-1-yl)phenoxy]phenoxy}-phenol and 3-[2,3,5,6-Tetra<\/em><em>\u044b<\/em><em>uoro-4-(3-hydroxyphenoxy)phenoxy]phenol. Changing the ratio of initial bisphenols allows to adjust the content of allyl groups and unsubstituted aromatic moieties in the main chain of the synthesized polymers while preserving the constant concentration of fluorine atoms. The influence of base NaH and K<\/em><em>2<\/em><em>CO<\/em><em>3<\/em><em>\u00a0on the molecular weight and mechanical properties of the synthesized copolymers was study.<\/em><\/p>\n<p><strong>\u00a0<\/strong><\/p>\n<p><strong>Key words:<\/strong> core-fluorinated aromatic polyethers, allyl-containing polyethers, copolymers, synthesis, properties.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>\u041b\u0438\u0442\u0435\u0440\u0430\u0442\u0443\u0440\u0430<\/strong><\/p>\n<p>1. Shevchenko V.V., Tkachenko I.M., Shekera O.V. \/\/ Polymer Sci. Part B. \u2013 2010. \u2013 52, \u2116 7\u20138. \u2013 P. 408 430.<br \/>\n2. Dhara M.G., Banerjee S. \/\/ Prog. Polym. Sci. \u2013 2010. \u2013 35, \u2116 7\u20138. \u2013 P. 1022 1077.<br \/>\n3. Wan Y., Zhang Y., Shi Z., Xu W., Zhang X., Zhao L., Cui Z. \/\/ Polymer. \u2013 2012. \u2013 53, \u2116 8. \u2013 P. 967 975.<br \/>\n4. Lee K.-S., Kim J.-P., Lee J.-S. \/\/ Polymer. \u2013 2010. \u2013 51, \u2116 3. \u2013 P. 632 638.<br \/>\n5. Tie W., Zhong Z., Wen P., Lee M.-H., Li X.-D. \/\/ Mater. Lett. \u2013 2009. \u2013 63, \u2116 16. \u2013 P. 1381\u20131383.<br \/>\n6. Li G., Wang J., Yu G., Jian X., Wang L., Zhao M. \/\/ Polymer. \u2013 2010. \u2013 51, \u2116 6. \u2013 P. 1524 1529.<br \/>\n7. Vainer A.Ya., Dyumaev K.M., Mareeva S.A., Gorb M.G., Desyatnik I.I., Tarnopolskii A.I. \/\/ Dokl. Chem. \u2013 2010. \u2013 432, Part 1. \u2013 P. 144\u2013147.<br \/>\n8. Lee K.-S., Jeong M.-H., Kim Y.-J., Lee S.-B., Lee J.-S. \/\/ Chem. Mater. \u2013 2012. \u2013 24, \u2116 8. \u2013 P. 1443&#8243;1453.<br \/>\n9. Wen P., Zhong Z., Li L., Zhang A., Li X.-D., Lee M.-H. \/\/ J. Mat. Chem. \u2013 2012. &#8211; 22, \u2116 41. \u2013 P. 22242\u201322249.<br \/>\n10. Lee K.-S., Jeong M.-H., Lee J.-S., Pivovar B.S., Kim Y.S. \/\/ J. Membr. Sci. \u2013 2010. &#8211; 352, \u2116 1-2. \u2013 P. 180\u2013188.<br \/>\n11. Jeong M.-H., Lee K.-S., Lee J.-S. \/\/ Macromolecules. \u2013 2009. \u2013 42, \u2116 5. \u2013 P. 1652-1658.<br \/>\n12. Lee K.-S., Lee J.-S. \/\/ Chem. Mater. \u2013 2006. \u2013 18, \u2116 18. \u2013 P. 4519-4525.<br \/>\n13. Ding J., Liu F., Li M., Day M., Zhou M. \/\/ J. Polym. Sci., Polym. Chem. \u2013 2002. \u2013 40, \u2116 23. P. 4205-4216.<br \/>\n14. Vainer A.Ya., Dyumaev K.M., Aronshtam N.E., Kornilova T.P., Levit E.I., Lozhkina I.M. \/\/ Doklady Chem. \u2013 2007. \u2013 412, Part II. \u2013 P. 38-41.<br \/>\n15. Feng S., Shang Y., Wang Y., Xie X., Mathur V.K., Xu J. \/\/ J. Power Sources. \u2013 2010. \u2013 195, \u2116 9. \u2013 P. 2541-2548.<br \/>\n16. Feng S., Shang Y., Xie X., Wang Y., Xu J. \/\/ J. Membr. Sci. \u2013 2009. \u2013 335, \u2116 1-2. \u2013 P. 13-20.<br \/>\n17. Ding F.C., Wang S.J., Xiao M., Meng Y.Z. \/\/ J. Power Sources. \u2013 2007. \u2013 164, \u2116 2. \u2013 P. 488-495.<br \/>\n18. Santhosh Kumar K.S., Reghunadhan Nair C.P., Radhakrishnan T.S., Ninan K.N. \/\/ Eur. Polym. J. \u2013 2007. \u2013 43, \u2116 6. \u2013 P. 2504-2514.<br \/>\n19. Gouri C., Reghunadhan Nair C.P., Ramaswamy R., Ninan K.N. \/\/ Eur. Polym. J. 2002. \u2013 38, \u2116 3. \u2013 P. 503-510.<br \/>\n20. Thankamony R.L., Won M., Kim T.-H. \/\/ Int. J. Hydrogen Energy. \u2013 2013. \u2013 38, \u2116 12. \u2013 P. 5084-5091.<br \/>\n21. Hoyle C.E., Bowman C.N. \/\/ Angew. Chem. Int. Ed. \u2013 2010. \u2013 49, \u2116 9. \u2013 P. 1540 \u20131573.<br \/>\n22. Hydrosilylation: A Comprehensive Review on Recent Advances \/\/ Marciniec B., Ed. \u2013 Springer: Berlin, Germany, 2009. \u2013 408 p.<br \/>\n23. Shree Varaprasad N.S., Venkhatesh P., Ramakrish-nan S. \/\/ J. Appl. Polym. Sci. \u2013 2014. \u2013 131, \u2116 10. \u2013 P. 40248.<br \/>\n24. Guan Z.P., Xiao M., Wang S.J., Meng Y.Z. \/\/ Eur. Polym. J. \u2013 2010. \u2013 46, \u2116 1. \u2013 P. 81 \u201391.<br \/>\n25. Brocas A.-L., Cendejas G., Caillol S., Deffieux A., Carlotti S. \/\/ J. Polym. Sci., Polym. Chem. \u2013 2011. \u2013 49, \u2116 12. \u2013 P. 2677-2684.<br \/>\n26. Putzien S., Nuyken O., Kuhn F.E. \/\/ Prog. Polym. Sci. \u2013 2010, &#8211; 35, \u2116 6. \u2013 P. 687\u2013713.<br \/>\n27. Tkachenko I.M., Shekera O.V., Shevchenko V.V. \/\/ Polym. Sci. Part. B. \u2013 2013. &#8211; 55, \u2116 5-6. \u2013 P. 336\u2013343.<br \/>\n28. Zhang S., Li C., Xie X., Zhang F. \/\/ Int. J. Hydrogen Energ. \u2013 2014. \u2013 http:\/\/dx.doi.org\/10.1016\/j.ijhydene.2014.03.122.<br \/>\n29. Qi Y., Jiang J., Callender C.L., Day M., Ding J. \/\/ Appl. Optics \u2013 2006. \u2013 45, \u2116 28. \u2013 P. 7480\u20137487.<br \/>\n30. Song Y., Wang J., Li G., Sun Q., Jian X., Teng J., Zhang H. \/\/ Polymer. \u2013 2008. &#8211; 49, \u2116 23. \u2013 P. 4995\u20135001.<br \/>\n31. Tkachenko I., Shekera O., Bliznyuk V., Shevchenko V. \/\/ J. Fluor. Chem. \u2013 2013. \u2013 149, \u2116 1. \u2013 P. 36\u201341.<br \/>\n32. \u041a\u0430\u043c\u0435\u043d\u0435\u0432\u0430 \u0422.\u041c., \u041c\u0430\u043b\u0438\u0447\u0435\u043d\u043a\u043e \u0411.\u0424., \u0428\u0435\u043b\u0443\u0434\u044c\u043a\u043e \u0415.\u0412., \u041f\u043e\u0433\u043e\u0440\u0435\u043b\u044b\u0439 \u0412.\u041a., \u0428\u0435\u0440\u0441\u0442\u044e\u043a \u0410.\u0418., \u0420\u043e\u0436\u0435\u043d\u043a\u043e \u0410.\u0411. \/\/ \u0416\u0443\u0440\u043d. \u043e\u0440\u0433. \u0445\u0438\u043c\u0438\u0438. \u2013 1989. \u2013 25, \u2116 3. \u2013 \u0421. 576-582.<br \/>\n33. \u0422\u043a\u0430\u0447\u0435\u043d\u043a\u043e \u0418.\u041c., \u041e\u0441\u0442\u0430\u043f\u044e\u043a \u0421.\u041d., \u0421\u0438\u0434\u043e\u0440\u0435\u043d\u043a\u043e \u0410.\u0412., \u0428\u0435\u043a\u0435\u0440\u0430 \u041e.\u0412., \u0428\u0435\u0432\u0447\u0435\u043d\u043a\u043e \u0412.\u0412. \/\/ \u0423\u043a\u0440. \u0445\u0438\u043c. \u0436\u0443\u0440\u043d. \u2013 2014. \u2013 80, \u2116 1. \u2013 \u0421. 63 68.<br \/>\n34. \u041e\u0440\u0433\u0430\u043d\u0438\u043a\u0443\u043c: \u0432 2-\u0445 \u0442. \/ \u041f\u0435\u0440. \u0441 \u043d\u0435\u043c. 4-\u0435 \u0438\u0437\u0434. \u2013 \u041c.: \u041c\u0438\u0440, 2008. \u2013 \u0422.2 \u2013 488 \u0441.<br \/>\n35. \u0428\u0435\u0432\u0447\u0435\u043d\u043a\u043e \u0412.\u0412., \u0422\u043a\u0430\u0447\u0435\u043d\u043a\u043e \u0418.\u041c., \u0413\u043e\u043c\u0437\u0430 \u042e.\u041f., \u0411\u043b\u0438\u0437-\u043d\u044e\u043a \u0412.\u041d., \u0428\u0435\u043a\u0435\u0440\u0430 \u041e.\u0412. \/\/ \u041f\u043e\u043b\u0438\u043c\u0435\u0440. \u0436\u0443\u0440\u043d. \u2013 2010. \u2013 32, \u2116 3. \u2013 \u0421. 243\u2013250.<br \/>\n36. Budd P.M., Ghanem B.S., Makhseed S., McKeown N.B., Msayib K.J., Tattershall C.E. \/\/ Chem. Commun. \u2013 2004. \u2013 \u2116 2. \u2013 P. 230\u2013231.<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>https:\/\/doi.org\/10.15407\/polymerj.37.02.168 Synthesis of allyl-containing poly(arylene ether)s copolymers with mono- and biphenylene fragments in main chain \u00a0 \u0406.\u041c. Tkachenko, A.V. Sidorenko, \u041e.V. Shekera, V.V. Shevchenko &nbsp; Institute of Macromolecular Chemistry NAS of Ukraine 48, Kharkivske shose, Kyiv, 02160, Ukraine &nbsp; Polym. J., 2015, 37, no. 2: 168-173. &nbsp; Section: Synthesis polymers. &nbsp; Language: Russian. &nbsp; Abstract: [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":[],"acf":[],"_links":{"self":[{"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages\/1889"}],"collection":[{"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/comments?post=1889"}],"version-history":[{"count":2,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages\/1889\/revisions"}],"predecessor-version":[{"id":2223,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages\/1889\/revisions\/2223"}],"wp:attachment":[{"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/media?parent=1889"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}