Syntheses and Investigation of Some New Polyarylates and Copolyarylates. Part I
By the interfacial condensation of acid chlorides I, II, and III, respectively, with bifunctional phenols (IV-X), soluble or mold-able thermostable polyarylates were obtained. Similarly, copolyarylates were prepared from a mixture of the acid chlorides I + II or I + III. With bisphenol-A (VIII), sol...
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Veröffentlicht in: | Journal of macromolecular science. Chemistry 1981-08, Vol.16 (3), p.651-668 |
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creator | Mansour, E. S. M. E. Khalifa, A. M. L. Rateb, L. |
description | By the interfacial condensation of acid chlorides I, II, and III, respectively, with bifunctional phenols (IV-X), soluble or mold-able thermostable polyarylates were obtained. Similarly, copolyarylates were prepared from a mixture of the acid chlorides I + II or I + III. With bisphenol-A (VIII), soluble polymers are usually obtained. Methylene dichloride and/or carbon tetra-chloride-water systems were the best media for interfacial condensations, and the polymers formed showed the highest reduced viscosity values.
Polyester films are useful in many industrial applications because of their broad range of mechanical, optical, and electrical properties. The aromatic polyesters-polyarylates-dominate the field of industrial polyester films [1].
Polyarylates prepared from dihydric phenols and purely aromatic dicarboxylic acid chlorides are highly heat resistant materials [2], but they are insoluble and nonmoldable [3]. However, by the introduction of ether linkages in the aromatic dicarboxylic acid moiety, soluble and/or moldable polyamides were obtained [4]. |
doi_str_mv | 10.1080/00222338108056813 |
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Polyester films are useful in many industrial applications because of their broad range of mechanical, optical, and electrical properties. The aromatic polyesters-polyarylates-dominate the field of industrial polyester films [1].
Polyarylates prepared from dihydric phenols and purely aromatic dicarboxylic acid chlorides are highly heat resistant materials [2], but they are insoluble and nonmoldable [3]. However, by the introduction of ether linkages in the aromatic dicarboxylic acid moiety, soluble and/or moldable polyamides were obtained [4].</description><identifier>ISSN: 0022-233X</identifier><identifier>DOI: 10.1080/00222338108056813</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><ispartof>Journal of macromolecular science. Chemistry, 1981-08, Vol.16 (3), p.651-668</ispartof><rights>Copyright Taylor & Francis Group, LLC 1981</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c213t-c8f3a3998eed7fec6faa50fc556d77d1cde1929da7383254d7dd6d3c9825cf373</citedby><cites>FETCH-LOGICAL-c213t-c8f3a3998eed7fec6faa50fc556d77d1cde1929da7383254d7dd6d3c9825cf373</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/00222338108056813$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/00222338108056813$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,59620,60409</link.rule.ids></links><search><creatorcontrib>Mansour, E. S. M. E.</creatorcontrib><creatorcontrib>Khalifa, A. M. L.</creatorcontrib><creatorcontrib>Rateb, L.</creatorcontrib><title>Syntheses and Investigation of Some New Polyarylates and Copolyarylates. Part I</title><title>Journal of macromolecular science. Chemistry</title><description>By the interfacial condensation of acid chlorides I, II, and III, respectively, with bifunctional phenols (IV-X), soluble or mold-able thermostable polyarylates were obtained. Similarly, copolyarylates were prepared from a mixture of the acid chlorides I + II or I + III. With bisphenol-A (VIII), soluble polymers are usually obtained. Methylene dichloride and/or carbon tetra-chloride-water systems were the best media for interfacial condensations, and the polymers formed showed the highest reduced viscosity values.
Polyester films are useful in many industrial applications because of their broad range of mechanical, optical, and electrical properties. The aromatic polyesters-polyarylates-dominate the field of industrial polyester films [1].
Polyarylates prepared from dihydric phenols and purely aromatic dicarboxylic acid chlorides are highly heat resistant materials [2], but they are insoluble and nonmoldable [3]. However, by the introduction of ether linkages in the aromatic dicarboxylic acid moiety, soluble and/or moldable polyamides were obtained [4].</description><issn>0022-233X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLAzEQgHNQsNT-AG_5A1vzMLtZ8CKLj0KxhSp4C0MeurKblCRY9t-7S3sQinMZ5mO-YWYQuqFkSYkkt4QwxjiXUyFKSfkFmk2sGOHHFVqk9E3GEILIks3QZjf4_GWTTRi8wSv_Y1NuPyG3wePg8C70Fr_aA96GboA4dJBPrU3Y_0FLvIWY8eoaXTrokl2c8hy9Pz2-NS_FevO8ah7WhWaU50JLx4HXtbTWVM7q0gEI4rQQpakqQ7WxtGa1gYpLzsSdqYwpDde1ZEI7XvE5ose5OoaUonVqH9t-3EZRoqbb1dkjRuf-6LTehdjDIcTOqAxDF6KL4HWbFP9f_wWwU2Xu</recordid><startdate>19810801</startdate><enddate>19810801</enddate><creator>Mansour, E. S. M. E.</creator><creator>Khalifa, A. M. L.</creator><creator>Rateb, L.</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19810801</creationdate><title>Syntheses and Investigation of Some New Polyarylates and Copolyarylates. Part I</title><author>Mansour, E. S. M. E. ; Khalifa, A. M. L. ; Rateb, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c213t-c8f3a3998eed7fec6faa50fc556d77d1cde1929da7383254d7dd6d3c9825cf373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Mansour, E. S. M. E.</creatorcontrib><creatorcontrib>Khalifa, A. M. L.</creatorcontrib><creatorcontrib>Rateb, L.</creatorcontrib><collection>CrossRef</collection><jtitle>Journal of macromolecular science. Chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mansour, E. S. M. E.</au><au>Khalifa, A. M. L.</au><au>Rateb, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Syntheses and Investigation of Some New Polyarylates and Copolyarylates. Part I</atitle><jtitle>Journal of macromolecular science. Chemistry</jtitle><date>1981-08-01</date><risdate>1981</risdate><volume>16</volume><issue>3</issue><spage>651</spage><epage>668</epage><pages>651-668</pages><issn>0022-233X</issn><abstract>By the interfacial condensation of acid chlorides I, II, and III, respectively, with bifunctional phenols (IV-X), soluble or mold-able thermostable polyarylates were obtained. Similarly, copolyarylates were prepared from a mixture of the acid chlorides I + II or I + III. With bisphenol-A (VIII), soluble polymers are usually obtained. Methylene dichloride and/or carbon tetra-chloride-water systems were the best media for interfacial condensations, and the polymers formed showed the highest reduced viscosity values.
Polyester films are useful in many industrial applications because of their broad range of mechanical, optical, and electrical properties. The aromatic polyesters-polyarylates-dominate the field of industrial polyester films [1].
Polyarylates prepared from dihydric phenols and purely aromatic dicarboxylic acid chlorides are highly heat resistant materials [2], but they are insoluble and nonmoldable [3]. However, by the introduction of ether linkages in the aromatic dicarboxylic acid moiety, soluble and/or moldable polyamides were obtained [4].</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/00222338108056813</doi><tpages>18</tpages></addata></record> |
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title | Syntheses and Investigation of Some New Polyarylates and Copolyarylates. Part I |
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