Hydroxyalkylation of parabanic acid. III. Polymers from parabanic acid and ethylene carbonate
The influence of initial molar ratio of reagents, amount of catalyst, and temperature of reaction between parabanic acid and ethylene carbonate on structure of product was studied. The reaction led to the opening of the trioxoimidazolidine ring, resulting in formation of thermally resistant linear p...
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| Veröffentlicht in: | Journal of applied polymer science 2006-04, Vol.100 (2), p.1443-1449 |
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| container_end_page | 1449 |
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| container_issue | 2 |
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| container_title | Journal of applied polymer science |
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| creator | Zarzyka-Niemiec, Iwona Naróg, Dorota Lubczak, Jacek |
| description | The influence of initial molar ratio of reagents, amount of catalyst, and temperature of reaction between parabanic acid and ethylene carbonate on structure of product was studied. The reaction led to the opening of the trioxoimidazolidine ring, resulting in formation of thermally resistant linear polymeric products constructed of urea and oxoamidoester subunits linked via imide bond. The percentage of side products was estimated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1443–1449, 2006 |
| doi_str_mv | 10.1002/app.23506 |
| format | Article |
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III. Polymers from parabanic acid and ethylene carbonate</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>The influence of initial molar ratio of reagents, amount of catalyst, and temperature of reaction between parabanic acid and ethylene carbonate on structure of product was studied. The reaction led to the opening of the trioxoimidazolidine ring, resulting in formation of thermally resistant linear polymeric products constructed of urea and oxoamidoester subunits linked via imide bond. The percentage of side products was estimated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1443–1449, 2006</description><subject>Applied sciences</subject><subject>ethylene carbonate</subject><subject>Exact sciences and technology</subject><subject>hydroxyalkylation</subject><subject>Organic polymers</subject><subject>parabanic acid</subject><subject>Physicochemistry of polymers</subject><subject>Polycondensation</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>ring-opening polymerization</subject><subject>structure</subject><subject>thermal stability</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLw0AUhQdRsFYX_oPZuHCRdB6ZTLqUom2g1SIVQZDhZjKDsWkSZgI2_95ofIDg6i7u9x0OB6FzSkJKCJtA04SMCxIfoBElUxlEMUsO0aj_0SCZTsUxOvH-lRBKe2iEnhdd7up9B-W2K6Et6grXFjfgIIOq0Bh0kYc4TdMQr-uy2xnnsXX17g-CocqxaV-60lQGa3BZXUFrTtGRhdKbs687Rg8315vZIljezdPZ1TLQnMs4EJHgkaHUEpYk0lhqE8JsJnKqE82M5maqo0z2pXXEsoRyzmhMRCR5LkQcxXyMLodc7WrvnbGqccUOXKcoUR-7qH4X9blLz14MbANeQ2kdVLrwv4LsuyRC9txk4N6K0nT_B6qr9fo7ORiMwrdm_2OA26pYcinU4-1cbVZP9F6uZorwd041f6Q</recordid><startdate>20060415</startdate><enddate>20060415</enddate><creator>Zarzyka-Niemiec, Iwona</creator><creator>Naróg, Dorota</creator><creator>Lubczak, Jacek</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20060415</creationdate><title>Hydroxyalkylation of parabanic acid. 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III. Polymers from parabanic acid and ethylene carbonate</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2006-04-15</date><risdate>2006</risdate><volume>100</volume><issue>2</issue><spage>1443</spage><epage>1449</epage><pages>1443-1449</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>The influence of initial molar ratio of reagents, amount of catalyst, and temperature of reaction between parabanic acid and ethylene carbonate on structure of product was studied. The reaction led to the opening of the trioxoimidazolidine ring, resulting in formation of thermally resistant linear polymeric products constructed of urea and oxoamidoester subunits linked via imide bond. The percentage of side products was estimated. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1443–1449, 2006</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/app.23506</doi><tpages>7</tpages></addata></record> |
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| subjects | Applied sciences ethylene carbonate Exact sciences and technology hydroxyalkylation Organic polymers parabanic acid Physicochemistry of polymers Polycondensation Preparation, kinetics, thermodynamics, mechanism and catalysts ring-opening polymerization structure thermal stability |
| title | Hydroxyalkylation of parabanic acid. III. Polymers from parabanic acid and ethylene carbonate |
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