Sulfide and sulfoxide based poly(ether-amide)s: Synthesis and characterization
Two new diacid monomers, 2,2′-sulfide bis(4-methyl phenoxy acetic acid) and 2,2′-sulfoxide bis(4-methyl phenoxy acetic acid) were successfully synthesized by refluxing the 2,2′-sulfide bis(4-methyl phenol) and 2,2′-sulfoxide bis(4-methyl phenol) with chloroacetonitrile in the presence of potassium c...
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Veröffentlicht in: | European polymer journal 2006, Vol.42 (1), p.133-139 |
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creator | Shockravi, Abbas Mehdipour-Ataei, Shahram Abouzari-Lotf, Ebrahim Yousefi, Ali |
description | Two new diacid monomers, 2,2′-sulfide bis(4-methyl phenoxy acetic acid) and 2,2′-sulfoxide bis(4-methyl phenoxy acetic acid) were successfully synthesized by refluxing the 2,2′-sulfide bis(4-methyl phenol) and 2,2′-sulfoxide bis(4-methyl phenol) with chloroacetonitrile in the presence of potassium carbonate, and subsequent basic reduction. Two novel series of poly(sulfide-ether-amide)s and poly(sulfoxide-ether-amide)s with aliphatic units in the main chain were prepared from diacids with various diamines.
The polyamides were obtained in quantitative yields and their inherent viscosities were in the range of 0.43–0.89
dl
g
−1 at a concentration of 0.5
g
dl
−1 in
N,
N-dimethylacetamide (DMAc) solvent at 25
°C. They showed good thermal stability. The temperature for 10% weight loss in argon atmosphere was in the range of 350–415
°C. The polymers showed glass transition temperatures between 228 and 261
°C. Almost all of the polyamides were readily soluble in a variety of polar solvents such as
N-methyl-2-pyrrolidone (NMP) and dimethyl sulfoxide (DMSO). |
doi_str_mv | 10.1016/j.eurpolymj.2005.06.031 |
format | Article |
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The polyamides were obtained in quantitative yields and their inherent viscosities were in the range of 0.43–0.89
dl
g
−1 at a concentration of 0.5
g
dl
−1 in
N,
N-dimethylacetamide (DMAc) solvent at 25
°C. They showed good thermal stability. The temperature for 10% weight loss in argon atmosphere was in the range of 350–415
°C. The polymers showed glass transition temperatures between 228 and 261
°C. Almost all of the polyamides were readily soluble in a variety of polar solvents such as
N-methyl-2-pyrrolidone (NMP) and dimethyl sulfoxide (DMSO).</description><identifier>ISSN: 0014-3057</identifier><identifier>EISSN: 1873-1945</identifier><identifier>DOI: 10.1016/j.eurpolymj.2005.06.031</identifier><identifier>CODEN: EUPJAG</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Exact sciences and technology ; Improved solubility ; Organic polymers ; Physicochemistry of polymers ; Poly(sulfide-ether-amide)s ; Poly(sulfoxide-ether-amide)s ; Polycondensation ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; Thermal stability</subject><ispartof>European polymer journal, 2006, Vol.42 (1), p.133-139</ispartof><rights>2005 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c376t-ea73860e1928b5bc6162b51ce3cee33ef17ca511e95ba356ee0741bcfefef7fa3</citedby><cites>FETCH-LOGICAL-c376t-ea73860e1928b5bc6162b51ce3cee33ef17ca511e95ba356ee0741bcfefef7fa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.eurpolymj.2005.06.031$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,4024,27923,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17410900$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Shockravi, Abbas</creatorcontrib><creatorcontrib>Mehdipour-Ataei, Shahram</creatorcontrib><creatorcontrib>Abouzari-Lotf, Ebrahim</creatorcontrib><creatorcontrib>Yousefi, Ali</creatorcontrib><title>Sulfide and sulfoxide based poly(ether-amide)s: Synthesis and characterization</title><title>European polymer journal</title><description>Two new diacid monomers, 2,2′-sulfide bis(4-methyl phenoxy acetic acid) and 2,2′-sulfoxide bis(4-methyl phenoxy acetic acid) were successfully synthesized by refluxing the 2,2′-sulfide bis(4-methyl phenol) and 2,2′-sulfoxide bis(4-methyl phenol) with chloroacetonitrile in the presence of potassium carbonate, and subsequent basic reduction. Two novel series of poly(sulfide-ether-amide)s and poly(sulfoxide-ether-amide)s with aliphatic units in the main chain were prepared from diacids with various diamines.
The polyamides were obtained in quantitative yields and their inherent viscosities were in the range of 0.43–0.89
dl
g
−1 at a concentration of 0.5
g
dl
−1 in
N,
N-dimethylacetamide (DMAc) solvent at 25
°C. They showed good thermal stability. The temperature for 10% weight loss in argon atmosphere was in the range of 350–415
°C. The polymers showed glass transition temperatures between 228 and 261
°C. Almost all of the polyamides were readily soluble in a variety of polar solvents such as
N-methyl-2-pyrrolidone (NMP) and dimethyl sulfoxide (DMSO).</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>Improved solubility</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Poly(sulfide-ether-amide)s</subject><subject>Poly(sulfoxide-ether-amide)s</subject><subject>Polycondensation</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>Thermal stability</subject><issn>0014-3057</issn><issn>1873-1945</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFUMtOwzAQtBBIlMI3kAsIDgnrOLYbblXFS6rgUDhbjrNRHeVR7BRRvh6XVnBEe9iHZmZ3h5BzCgkFKm7qBNdu1Tebtk5SAJ6ASIDRAzKiE8limmf8kIwAaBYz4PKYnHhfA4Bkgo3I82LdVLbESHdl5EPdf267Qnsso63qFQ5LdLFuw_ja30aLTRcG3vofhllqp82Azn7pwfbdKTmqdOPxbJ_H5O3-7nX2GM9fHp5m03lsmBRDjFqyiQCkeTopeGEEFWnBqUFmEBnDikqjOaWY80IzLhBBZrQwFYaQlWZjcrnTXbn-fY1-UK31BptGd9ivvUpzLlMuswCUO6BxvfcOK7VyttVuoyiorX-qVr_-qa1_CoQK_gXmxX6F9kY3ldOdsf6PHg6CHCDgpjschn8_LDrljcXOYGkdmkGVvf131zfas4yt</recordid><startdate>2006</startdate><enddate>2006</enddate><creator>Shockravi, Abbas</creator><creator>Mehdipour-Ataei, Shahram</creator><creator>Abouzari-Lotf, Ebrahim</creator><creator>Yousefi, Ali</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>2006</creationdate><title>Sulfide and sulfoxide based poly(ether-amide)s: Synthesis and characterization</title><author>Shockravi, Abbas ; Mehdipour-Ataei, Shahram ; Abouzari-Lotf, Ebrahim ; Yousefi, Ali</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c376t-ea73860e1928b5bc6162b51ce3cee33ef17ca511e95ba356ee0741bcfefef7fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>Improved solubility</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Poly(sulfide-ether-amide)s</topic><topic>Poly(sulfoxide-ether-amide)s</topic><topic>Polycondensation</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>Thermal stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shockravi, Abbas</creatorcontrib><creatorcontrib>Mehdipour-Ataei, Shahram</creatorcontrib><creatorcontrib>Abouzari-Lotf, Ebrahim</creatorcontrib><creatorcontrib>Yousefi, Ali</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>European polymer journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shockravi, Abbas</au><au>Mehdipour-Ataei, Shahram</au><au>Abouzari-Lotf, Ebrahim</au><au>Yousefi, Ali</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sulfide and sulfoxide based poly(ether-amide)s: Synthesis and characterization</atitle><jtitle>European polymer journal</jtitle><date>2006</date><risdate>2006</risdate><volume>42</volume><issue>1</issue><spage>133</spage><epage>139</epage><pages>133-139</pages><issn>0014-3057</issn><eissn>1873-1945</eissn><coden>EUPJAG</coden><abstract>Two new diacid monomers, 2,2′-sulfide bis(4-methyl phenoxy acetic acid) and 2,2′-sulfoxide bis(4-methyl phenoxy acetic acid) were successfully synthesized by refluxing the 2,2′-sulfide bis(4-methyl phenol) and 2,2′-sulfoxide bis(4-methyl phenol) with chloroacetonitrile in the presence of potassium carbonate, and subsequent basic reduction. Two novel series of poly(sulfide-ether-amide)s and poly(sulfoxide-ether-amide)s with aliphatic units in the main chain were prepared from diacids with various diamines.
The polyamides were obtained in quantitative yields and their inherent viscosities were in the range of 0.43–0.89
dl
g
−1 at a concentration of 0.5
g
dl
−1 in
N,
N-dimethylacetamide (DMAc) solvent at 25
°C. They showed good thermal stability. The temperature for 10% weight loss in argon atmosphere was in the range of 350–415
°C. The polymers showed glass transition temperatures between 228 and 261
°C. Almost all of the polyamides were readily soluble in a variety of polar solvents such as
N-methyl-2-pyrrolidone (NMP) and dimethyl sulfoxide (DMSO).</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.eurpolymj.2005.06.031</doi><tpages>7</tpages></addata></record> |
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source | Elsevier ScienceDirect Journals Complete |
subjects | Applied sciences Exact sciences and technology Improved solubility Organic polymers Physicochemistry of polymers Poly(sulfide-ether-amide)s Poly(sulfoxide-ether-amide)s Polycondensation Preparation, kinetics, thermodynamics, mechanism and catalysts Thermal stability |
title | Sulfide and sulfoxide based poly(ether-amide)s: Synthesis and characterization |
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