Loading…

Microstructural analysis of p-acryloyloxy-acetanilide and N, N-dimethylacrylamide copolymers of biomedical interest by NMR

Copolymers with anti-thrombogenic properties based on N,N-dimethylacrylamide (A) and para-acryloyloxyacetanilide (B) were prepared by radical polymerization in DMF solutions at 50 degree C using 2,2'-azobisisobutyronitrile (AIBN) as initiator. The reactivity ratios of both monomers were determi...

Full description

Saved in:
Bibliographic Details
Published in:Polymer (Guilford) 1999-08, Vol.40 (17), p.4953-4960
Main Authors: BULAI, A, DE QUEIROZ, A.-A. A, GALLARDO, A, ROMAN, J. S
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c311t-e996ecfcb9f748fb5f304b17028fda07aef90ad8e58624aed4644907faeb9be93
cites cdi_FETCH-LOGICAL-c311t-e996ecfcb9f748fb5f304b17028fda07aef90ad8e58624aed4644907faeb9be93
container_end_page 4960
container_issue 17
container_start_page 4953
container_title Polymer (Guilford)
container_volume 40
creator BULAI, A
DE QUEIROZ, A.-A. A
GALLARDO, A
ROMAN, J. S
description Copolymers with anti-thrombogenic properties based on N,N-dimethylacrylamide (A) and para-acryloyloxyacetanilide (B) were prepared by radical polymerization in DMF solutions at 50 degree C using 2,2'-azobisisobutyronitrile (AIBN) as initiator. The reactivity ratios of both monomers were determined by the application of the non-linear least-squares method suggested by Tidwell and Mortimer. The obtained results (r sub(A) identical with 0.47 and r sub(B) identical with 0.63) confirm that this comonomer pair polymerizes statistically but with a moderate tendency to form alternate sequences, depending on the composition of the monomer feed.
doi_str_mv 10.1016/S0032-3861(98)00710-1
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_21411290</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>402215</sourcerecordid><originalsourceid>FETCH-LOGICAL-c311t-e996ecfcb9f748fb5f304b17028fda07aef90ad8e58624aed4644907faeb9be93</originalsourceid><addsrcrecordid>eNpFkNtKxDAQhoMouB4eQeiFiILVmbTbNJcinsBdwcN1SNMJRtJ2TbpgfXq766IQmMB88w_zMXaEcIGAxeULQMbTrCzwVJZnAAIhxS02wVJkKecSt9nkD9llezF-AACf8nzCvmfOhC72YWn6ZdA-0a32Q3Qx6WyySLUJg-_G9zWMf-p167yraaTqZH6ezNPaNdS_D34N6mbVM92i80NDYZ1Rua6h2pkx2rU9BYp9Ug3JfPZ8wHas9pEON3Wfvd3evF7fp49Pdw_XV4-pyRD7lKQsyFhTSSvy0lZTm0FeoQBe2lqD0GQl6LqkaVnwXFOdF3kuQVhNlaxIZvvs5Dd3EbrP5bhfNS4a8l631C2j4pgjcgkjOP0FV0ZiIKsWwTU6DApBrUyrtWm10qhkqdamFY5zx5sFOo532qBb4-L_sBBcCMx-AJK0gXc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>21411290</pqid></control><display><type>article</type><title>Microstructural analysis of p-acryloyloxy-acetanilide and N, N-dimethylacrylamide copolymers of biomedical interest by NMR</title><source>ScienceDirect Journals</source><creator>BULAI, A ; DE QUEIROZ, A.-A. A ; GALLARDO, A ; ROMAN, J. S</creator><creatorcontrib>BULAI, A ; DE QUEIROZ, A.-A. A ; GALLARDO, A ; ROMAN, J. S</creatorcontrib><description>Copolymers with anti-thrombogenic properties based on N,N-dimethylacrylamide (A) and para-acryloyloxyacetanilide (B) were prepared by radical polymerization in DMF solutions at 50 degree C using 2,2'-azobisisobutyronitrile (AIBN) as initiator. The reactivity ratios of both monomers were determined by the application of the non-linear least-squares method suggested by Tidwell and Mortimer. The obtained results (r sub(A) identical with 0.47 and r sub(B) identical with 0.63) confirm that this comonomer pair polymerizes statistically but with a moderate tendency to form alternate sequences, depending on the composition of the monomer feed.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/S0032-3861(98)00710-1</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Oxford: Elsevier</publisher><subject>Acrylics ; Applied sciences ; Biomedical engineering ; Biopolymers ; Chemical bonds ; Exact sciences and technology ; Free radical polymerization ; Microstructure ; Nuclear magnetic resonance spectroscopy ; Organic polymers ; Physicochemistry of polymers ; Polyamides ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; Structure (composition)</subject><ispartof>Polymer (Guilford), 1999-08, Vol.40 (17), p.4953-4960</ispartof><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c311t-e996ecfcb9f748fb5f304b17028fda07aef90ad8e58624aed4644907faeb9be93</citedby><cites>FETCH-LOGICAL-c311t-e996ecfcb9f748fb5f304b17028fda07aef90ad8e58624aed4644907faeb9be93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1772771$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>BULAI, A</creatorcontrib><creatorcontrib>DE QUEIROZ, A.-A. A</creatorcontrib><creatorcontrib>GALLARDO, A</creatorcontrib><creatorcontrib>ROMAN, J. S</creatorcontrib><title>Microstructural analysis of p-acryloyloxy-acetanilide and N, N-dimethylacrylamide copolymers of biomedical interest by NMR</title><title>Polymer (Guilford)</title><description>Copolymers with anti-thrombogenic properties based on N,N-dimethylacrylamide (A) and para-acryloyloxyacetanilide (B) were prepared by radical polymerization in DMF solutions at 50 degree C using 2,2'-azobisisobutyronitrile (AIBN) as initiator. The reactivity ratios of both monomers were determined by the application of the non-linear least-squares method suggested by Tidwell and Mortimer. The obtained results (r sub(A) identical with 0.47 and r sub(B) identical with 0.63) confirm that this comonomer pair polymerizes statistically but with a moderate tendency to form alternate sequences, depending on the composition of the monomer feed.</description><subject>Acrylics</subject><subject>Applied sciences</subject><subject>Biomedical engineering</subject><subject>Biopolymers</subject><subject>Chemical bonds</subject><subject>Exact sciences and technology</subject><subject>Free radical polymerization</subject><subject>Microstructure</subject><subject>Nuclear magnetic resonance spectroscopy</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polyamides</subject><subject>Polymers with particular properties</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>Structure (composition)</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNpFkNtKxDAQhoMouB4eQeiFiILVmbTbNJcinsBdwcN1SNMJRtJ2TbpgfXq766IQmMB88w_zMXaEcIGAxeULQMbTrCzwVJZnAAIhxS02wVJkKecSt9nkD9llezF-AACf8nzCvmfOhC72YWn6ZdA-0a32Q3Qx6WyySLUJg-_G9zWMf-p167yraaTqZH6ezNPaNdS_D34N6mbVM92i80NDYZ1Rua6h2pkx2rU9BYp9Ug3JfPZ8wHas9pEON3Wfvd3evF7fp49Pdw_XV4-pyRD7lKQsyFhTSSvy0lZTm0FeoQBe2lqD0GQl6LqkaVnwXFOdF3kuQVhNlaxIZvvs5Dd3EbrP5bhfNS4a8l631C2j4pgjcgkjOP0FV0ZiIKsWwTU6DApBrUyrtWm10qhkqdamFY5zx5sFOo532qBb4-L_sBBcCMx-AJK0gXc</recordid><startdate>19990801</startdate><enddate>19990801</enddate><creator>BULAI, A</creator><creator>DE QUEIROZ, A.-A. A</creator><creator>GALLARDO, A</creator><creator>ROMAN, J. S</creator><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19990801</creationdate><title>Microstructural analysis of p-acryloyloxy-acetanilide and N, N-dimethylacrylamide copolymers of biomedical interest by NMR</title><author>BULAI, A ; DE QUEIROZ, A.-A. A ; GALLARDO, A ; ROMAN, J. S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c311t-e996ecfcb9f748fb5f304b17028fda07aef90ad8e58624aed4644907faeb9be93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Acrylics</topic><topic>Applied sciences</topic><topic>Biomedical engineering</topic><topic>Biopolymers</topic><topic>Chemical bonds</topic><topic>Exact sciences and technology</topic><topic>Free radical polymerization</topic><topic>Microstructure</topic><topic>Nuclear magnetic resonance spectroscopy</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polyamides</topic><topic>Polymers with particular properties</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>Structure (composition)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>BULAI, A</creatorcontrib><creatorcontrib>DE QUEIROZ, A.-A. A</creatorcontrib><creatorcontrib>GALLARDO, A</creatorcontrib><creatorcontrib>ROMAN, J. S</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>BULAI, A</au><au>DE QUEIROZ, A.-A. A</au><au>GALLARDO, A</au><au>ROMAN, J. S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microstructural analysis of p-acryloyloxy-acetanilide and N, N-dimethylacrylamide copolymers of biomedical interest by NMR</atitle><jtitle>Polymer (Guilford)</jtitle><date>1999-08-01</date><risdate>1999</risdate><volume>40</volume><issue>17</issue><spage>4953</spage><epage>4960</epage><pages>4953-4960</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><coden>POLMAG</coden><abstract>Copolymers with anti-thrombogenic properties based on N,N-dimethylacrylamide (A) and para-acryloyloxyacetanilide (B) were prepared by radical polymerization in DMF solutions at 50 degree C using 2,2'-azobisisobutyronitrile (AIBN) as initiator. The reactivity ratios of both monomers were determined by the application of the non-linear least-squares method suggested by Tidwell and Mortimer. The obtained results (r sub(A) identical with 0.47 and r sub(B) identical with 0.63) confirm that this comonomer pair polymerizes statistically but with a moderate tendency to form alternate sequences, depending on the composition of the monomer feed.</abstract><cop>Oxford</cop><pub>Elsevier</pub><doi>10.1016/S0032-3861(98)00710-1</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0032-3861
ispartof Polymer (Guilford), 1999-08, Vol.40 (17), p.4953-4960
issn 0032-3861
1873-2291
language eng
recordid cdi_proquest_miscellaneous_21411290
source ScienceDirect Journals
subjects Acrylics
Applied sciences
Biomedical engineering
Biopolymers
Chemical bonds
Exact sciences and technology
Free radical polymerization
Microstructure
Nuclear magnetic resonance spectroscopy
Organic polymers
Physicochemistry of polymers
Polyamides
Polymers with particular properties
Preparation, kinetics, thermodynamics, mechanism and catalysts
Structure (composition)
title Microstructural analysis of p-acryloyloxy-acetanilide and N, N-dimethylacrylamide copolymers of biomedical interest by NMR
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T11%3A20%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Microstructural%20analysis%20of%20p-acryloyloxy-acetanilide%20and%20N,%20N-dimethylacrylamide%20copolymers%20of%20biomedical%20interest%20by%20NMR&rft.jtitle=Polymer%20(Guilford)&rft.au=BULAI,%20A&rft.date=1999-08-01&rft.volume=40&rft.issue=17&rft.spage=4953&rft.epage=4960&rft.pages=4953-4960&rft.issn=0032-3861&rft.eissn=1873-2291&rft.coden=POLMAG&rft_id=info:doi/10.1016/S0032-3861(98)00710-1&rft_dat=%3Cproquest_cross%3E402215%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c311t-e996ecfcb9f748fb5f304b17028fda07aef90ad8e58624aed4644907faeb9be93%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=21411290&rft_id=info:pmid/&rfr_iscdi=true