{"id":1945,"date":"2018-01-10T17:48:38","date_gmt":"2018-01-10T14:48:38","guid":{"rendered":"http:\/\/polymerjournal.kiev.ua\/en\/?page_id=1945"},"modified":"2018-02-14T17:29:22","modified_gmt":"2018-02-14T14:29:22","slug":"2015-3-11","status":"publish","type":"page","link":"http:\/\/polymerjournal.kiev.ua\/en\/2015-3-11\/","title":{"rendered":"2015 (3) 11"},"content":{"rendered":"<p><a href=\"https:\/\/doi.org\/10.15407\/polymerj.37.03.293\">https:\/\/doi.org\/10.15407\/polymerj.37.03.293<\/a><\/p>\n<p><strong>Organic-inorganics\u00a0 silsesquioxanes nanohybrides <\/strong><strong>\u0441<\/strong><strong>omp<\/strong><strong>\u043e<\/strong><strong>sing\u00a0 quaternary\u00a0 amines<\/strong><\/p>\n<p><strong>\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 <\/strong><\/p>\n<p><strong><em>L.P. Robota, V. G. Sierov, V.I. Litviakov, Yu.V. Savelyev<\/em><\/strong><\/p>\n<p><strong><em>\u00a0<\/em><\/strong><\/p>\n<p>Institute of Macromolecular Chemistry the 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. 3: 293-298.<\/p>\n<p>&nbsp;<\/p>\n<p>Section: Structure and properties.<\/p>\n<p>&nbsp;<\/p>\n<p>Language: Russian.<\/p>\n<p>&nbsp;<\/p>\n<p>Abstract:<\/p>\n<p><em>Urethaneureasilsesquioxane precursors based on polyethylene glycol -1000 (PEG-1000), 1,6-hexamethylene diisocyanate (1,6-HMDI) and 3-aminopropyltriethoxysilane (APTES) as well as their analogues containing crownether and benzidine fragments in the chain have been obtained.<\/em><\/p>\n<p><em>The biologically-active compound 1,2-ethylene-bis-(N-dimethyl-carbdecyloksimethyl)-carbmenthoxymethyl)-ammonium dichloride (ethonium) was introduced in dimethylformamide (DMFA) solutions of precursors at a molar ratio of precursor: ethonium of 1,0\/0,5; 1,0\/1,0 and 1,0\/2,5. We used NN4F as catalyst for the hydrolytic polycondensation. Polyurethaneureasilsesquioxane films were prepared by gelling from solutions. The composition of precursors and their polycondensation products has been confirmed by IR spectroscopic studies. <\/em><em>NMR studies have shown that the intermolecular interaction of the prepolymer and quaternary amine takes place primarily through the interaction of urea groups of the prepolymer and the amine anions in the absence of significant changes in the absorption region of urethane associates. Monitoring of the degree of release of 1,2-ethylene-bis-(N-dimethyl- dimethyl-carbdecyloksimethyl)- carbmenthoxymethyl)-ammonium dichloride in distilled water, was studied using the conductometric method.<\/em><\/p>\n<p><em>\u00a0<\/em><\/p>\n<p><strong>Key words: <\/strong>polyurethane(urea)silsesquioxanes, crown ethers, non covalent interactions, quarternary amines.<\/p>\n<p>&nbsp;<\/p>\n<p><strong>\u041b\u0438\u0442\u0435\u0440\u0430\u0442\u0443\u0440\u0430<\/strong><\/p>\n<p>1. Bosman A.W, Sijbesma R.P, Meijer E.W. \/\/ Materials Today.- 2004.- 7, \u2116 4.- \u0420. 34-39.<br \/>\n2. Hillberg A L, Tabrizian M. \/\/ Biomolecule imprinting: Developments in mimicking dynamic natural recognition systems IRBM.- 2008.- 29, \u2116 2-3.- \u0420.89-104.<br \/>\n3. Miyata Takashi, Uragami Tadashi, Nakamae Katsuhiko \/\/ Advanced Drug Delivery Reviews.- 2002.- 54, \u2116 1.- \u0420.79-98.<br \/>\n4. Huai-Ping Cong, Shu-Hong Yu \/\/ Current Opinion in Colloid &amp; Interface Science.-2009.- 14, \u2116 2. &#8211; \u0420. 71\u201380.<br \/>\n5. In^es Rosane W.Z. de Oliveira, Renata El-Hage M. de Barros Os\u2019orio, Ademir Neves, Iolanda Cruz Vieira \/\/ Sensors and Actuators B.- 2007.- 122, \u2116 1.- P. 89\u201394.<br \/>\n6. \u0421\u0435\u0440\u043e\u0432 \u0412.\u0413., \u041b\u0438\u0442\u0432\u044f\u043a\u043e\u0432 \u0412.\u0418., \u0420\u043e\u0431\u043e\u0442\u0430 \u041b.\u041f., \u0421\u0430\u0432\u0435\u043b\u044c- \u0435\u0432 \u042e.\u0412. \/\/ \u0423\u043a\u0440. \u0445\u0456\u043c. \u0436\u0443\u0440\u043d. \u2013 2009. \u2013 75, \u2116 6. \u2013 \u0421. 60\u201364.<br \/>\n7. Chih-Ping Chen, Shenghong A. Dai, Huey-Ling Chang, Wen-Chiung Su, Tzong-Ming Wu, Ru-Jong Jeng \/\/ Polymer.- 2005.- 46, \u211625.- P. 11849\u201311857.<br \/>\n8. Jin Seok Lee, Yun-Jo Lee, Eunju Lee Tae, Yong Soo Park, Kyung Byung Yoon \/\/ Science. -2003.- 301.- \u0420. 818-821.<br \/>\n9. M.Y. Grigoreva \/\/ Biotechnologia Acta. \u2013 2013.- 6, \u2116 5.- \u0420. 41-48.<br \/>\n10. Soletti L., Hong Y., Guan J., Stankus J. J., El-Kurdi M. S., Wagner W. R. \/\/ Acta Biomater. &#8211; 2010. &#8211; 6.- \u0420. 110\u201322.<br \/>\n11. Nieponice A., Nieponice A., Soletti L., Guan J., Hong Y., Gharaibeh B., Maul T. M. \/\/ Tissue Eng. Part. \u2013 2010. \u2013 16, \u2116 4. &#8211; \u0420. 1215\u201323.<br \/>\n12. de-Mel A., de-Mel A., Murad F., Seifalian A.M. \/\/ Chem. Rev. \u2013 2011.- 111, \u2116 9 \u2013 \u0420. 5742-5767.<br \/>\n13. Pan Q., Fan X., Chen X., Zhou Q. \/\/ Huaxue Jinzhan. &#8211; 2006. \u2013 18, \u2116 5.- \u0420. 616-621.<br \/>\n14. Banchob Wanno, Wandee Rakrai, Somchai Keawwangchai, Neramit Morakot, Nongnit Morakot, Nadtanet Nunthaboot, Vithaya Ruangpornvisuti \/\/ J. of Molecular Structure: THEOCHEM.- 2009.- 902, \u2116 1-3. \u2013 \u0420. 33\u201340.<br \/>\n15. \u0425\u0438\u0440\u0430\u043e\u043a\u0430 \u041c. \u041a\u0440\u0430\u0443\u043d-\u0441\u043e\u0435\u0434\u0438\u043d\u0435\u043d\u0438\u044f. \u0421\u0432\u043e\u0439\u0441\u0442\u0432\u0430 \u0438 \u043f\u0440\u0438\u043c\u0435\u043d\u0435\u043d\u0438\u0435. \/ \u041f\u0435\u0440. \u0441 \u0430\u043d\u0433\u043b.- \u041c.: \u041c\u0438\u0440, 1986.- 363 \u0441.<br \/>\n16. \u0421\u0435\u0440\u043e\u0432 \u0412.\u0413., \u041b\u0438\u0442\u0432\u044f\u043a\u043e\u0432 \u0412.\u0418., \u0420\u043e\u0431\u043e\u0442\u0430 \u041b.\u041f., \u041f\u0440\u0438\u0432\u0430\u043b-\u043a\u043e \u042d.\u0413., \u0421\u0430\u0432\u0435\u043b\u044c\u0435\u0432 \u042e.\u0412. \/\/ \u041f\u043e\u043b\u0456\u043c\u0435\u0440. \u0436\u0443\u0440\u043d. \u2013 2009. \u2013 31, \u2116 2. \u2013 \u0421. 156\u2013161.<\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>https:\/\/doi.org\/10.15407\/polymerj.37.03.293 Organic-inorganics\u00a0 silsesquioxanes nanohybrides \u0441omp\u043esing\u00a0 quaternary\u00a0 amines \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 L.P. Robota, V. G. Sierov, V.I. Litviakov, Yu.V. Savelyev \u00a0 Institute of Macromolecular Chemistry the NAS of Ukraine 48, Kharkivske shose, Kyiv, 02160, Ukraine &nbsp; Polym. J., 2015, 37, no. 3: 293-298. &nbsp; Section: Structure and properties. &nbsp; Language: Russian. &nbsp; Abstract: Urethaneureasilsesquioxane precursors based on polyethylene [&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\/1945"}],"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=1945"}],"version-history":[{"count":2,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages\/1945\/revisions"}],"predecessor-version":[{"id":2209,"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/pages\/1945\/revisions\/2209"}],"wp:attachment":[{"href":"http:\/\/polymerjournal.kiev.ua\/en\/wp-json\/wp\/v2\/media?parent=1945"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}