13 C NMR spectral assignments of methacrylic acid/acrylonitrile statistical copolymers
Copolymerization of methacrylic acid (M) and acrylonitrile (A) in bulk at 60°C gives a statistical copolymer. Through the use of 1 H, 13 C, DEPT and twodimensional NMR techniques, the observed resonances in the NMR spectra of these copolymers can be assigned, and thus provide detailed information ab...
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Veröffentlicht in: | Polymer international 1991-01, Vol.26 (3), p.171-179 |
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container_title | Polymer international |
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creator | Borbely, Janos D. Hill, David J. T. Lang, Anthony P. O'Donnell, James H. |
description | Copolymerization of methacrylic acid (M) and acrylonitrile (A) in bulk at 60°C gives a statistical copolymer. Through the use of
1
H,
13
C, DEPT and twodimensional NMR techniques, the observed resonances in the NMR spectra of these copolymers can be assigned, and thus provide detailed information about the microstructure of the polymer at the diad, triad and tetrad levels. Configurational effects have also been shown to play an important role, although in all cases the chemical shift differences resulting from configurational variation are smaller than those resulting from sequence variation. |
doi_str_mv | 10.1002/pi.4990260309 |
format | Article |
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1
H,
13
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1
H,
13
C, DEPT and twodimensional NMR techniques, the observed resonances in the NMR spectra of these copolymers can be assigned, and thus provide detailed information about the microstructure of the polymer at the diad, triad and tetrad levels. Configurational effects have also been shown to play an important role, although in all cases the chemical shift differences resulting from configurational variation are smaller than those resulting from sequence variation.</description><issn>0959-8103</issn><issn>1097-0126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNpFkEtLxDAUhYMoOI4u3ecPZOamaTO9Sym-YFSQwW1JbxKN9EWSTf-94wNcHc7ifBw-xq4lbCRAsZ3DpkSEQoMCPGErCbgTIAt9ylaAFYpagjpnFyl9AkCNiCv2JhVv-PPTK0-zoxxNz01K4X0c3JgTnzwfXP4wFJc-EDcU7PanTGPIMfSOp2xySDnQcUnTPPXL4GK6ZGfe9Mld_eWaHe5uD82D2L_cPzY3e0F1gULrTpfQaV8jYS1lJ423uqPKu7JSpJUzFWlPx7NkytpYkk5ZtGBxVxW-VGsmfrEUp5Si8-0cw2Di0kpov520c2j_nagvnAdWPA</recordid><startdate>199101</startdate><enddate>199101</enddate><creator>Borbely, Janos D.</creator><creator>Hill, David J. T.</creator><creator>Lang, Anthony P.</creator><creator>O'Donnell, James H.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199101</creationdate><title>13 C NMR spectral assignments of methacrylic acid/acrylonitrile statistical copolymers</title><author>Borbely, Janos D. ; Hill, David J. T. ; Lang, Anthony P. ; O'Donnell, James H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c829-66b640b6f89c9811b1afd6bc5fe453c63ea5c6fc008ca48adc1e3d9d0d9752f43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borbely, Janos D.</creatorcontrib><creatorcontrib>Hill, David J. T.</creatorcontrib><creatorcontrib>Lang, Anthony P.</creatorcontrib><creatorcontrib>O'Donnell, James H.</creatorcontrib><collection>CrossRef</collection><jtitle>Polymer international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borbely, Janos D.</au><au>Hill, David J. T.</au><au>Lang, Anthony P.</au><au>O'Donnell, James H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>13 C NMR spectral assignments of methacrylic acid/acrylonitrile statistical copolymers</atitle><jtitle>Polymer international</jtitle><date>1991-01</date><risdate>1991</risdate><volume>26</volume><issue>3</issue><spage>171</spage><epage>179</epage><pages>171-179</pages><issn>0959-8103</issn><eissn>1097-0126</eissn><abstract>Copolymerization of methacrylic acid (M) and acrylonitrile (A) in bulk at 60°C gives a statistical copolymer. Through the use of
1
H,
13
C, DEPT and twodimensional NMR techniques, the observed resonances in the NMR spectra of these copolymers can be assigned, and thus provide detailed information about the microstructure of the polymer at the diad, triad and tetrad levels. Configurational effects have also been shown to play an important role, although in all cases the chemical shift differences resulting from configurational variation are smaller than those resulting from sequence variation.</abstract><doi>10.1002/pi.4990260309</doi><tpages>9</tpages></addata></record> |
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language | eng |
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source | Wiley Journals |
title | 13 C NMR spectral assignments of methacrylic acid/acrylonitrile statistical copolymers |
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