Flexibilized styrene-N-substituted maleimide copolymers. II. Multiblock copolymers prepared from PTHF-based iniferters

2000; Wiley; Volume: 38; Issue: 19 Linguagem: Inglês

10.1002/1099-0518(20001001)38

ISSN

1099-0518

Autores

Davy R. Suwier, Marcel N. Teerenstra, Bert Vanhaecht, Cornelis Koning,

Tópico(s)

Inorganic and Organometallic Chemistry

Resumo

Journal of Polymer Science Part A: Polymer ChemistryVolume 38, Issue 19 p. 3558-3568 Article Flexibilized styrene–N-substituted maleimide copolymers. II. Multiblock copolymers prepared from PTHF-based iniferters D. R. Suwier, D. R. Suwier Department of Physical and Colloid Chemistry, Free University of Brussels (VUB), Pleinlaan 2, 1050 Brussels, BelgiumSearch for more papers by this authorM. N. Teerenstra, M. N. Teerenstra Department of Physical and Colloid Chemistry, Free University of Brussels (VUB), Pleinlaan 2, 1050 Brussels, BelgiumSearch for more papers by this authorB. Vanhaecht, B. Vanhaecht Department of Physical and Colloid Chemistry, Free University of Brussels (VUB), Pleinlaan 2, 1050 Brussels, Belgium Research assistant at the Fund for Scientific Research, Flanders, Belgium (FWO)Search for more papers by this authorC. E. Koning, Corresponding Author C. E. Koning DSM Research, P.O. Box 18, 6160 MD Geleen, The NetherlandsDSM Research, P.O. Box 18, 6160 MD Geleen, The NetherlandsSearch for more papers by this author D. R. Suwier, D. R. Suwier Department of Physical and Colloid Chemistry, Free University of Brussels (VUB), Pleinlaan 2, 1050 Brussels, BelgiumSearch for more papers by this authorM. N. Teerenstra, M. N. Teerenstra Department of Physical and Colloid Chemistry, Free University of Brussels (VUB), Pleinlaan 2, 1050 Brussels, BelgiumSearch for more papers by this authorB. Vanhaecht, B. Vanhaecht Department of Physical and Colloid Chemistry, Free University of Brussels (VUB), Pleinlaan 2, 1050 Brussels, Belgium Research assistant at the Fund for Scientific Research, Flanders, Belgium (FWO)Search for more papers by this authorC. E. Koning, Corresponding Author C. E. Koning DSM Research, P.O. Box 18, 6160 MD Geleen, The NetherlandsDSM Research, P.O. Box 18, 6160 MD Geleen, The NetherlandsSearch for more papers by this author First published: 11 August 2000 https://doi.org/10.1002/1099-0518(20001001)38:19 3.0.CO;2-TCitations: 14 Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Abstract This article describes the synthesis and molecular characterization of thermal polymeric iniferters, based on hydroxy-terminated poly(tetrahydrofuran) (PTHF), bearing thiuram disulfide groups along the chain. Thermal polymerization after the addition of styrene (S) and N-methylmaleimide (MI) to these PTHF-based polymeric iniferters yielded segmented PTHF (SMI-block-PTHF)n block copolymers that proved to have a single Tg. The multiblock copolymers were molecularly characterized by elemental analysis, IR, and NMR. The thermal stability, as checked by thermogravimetric analysis, proved to be good up to about 350 °C. A size exclusion chromatography/differential viscosity (DV) analysis showed that the molecular weights of the synthesized single-phase multiblock copolymers were sufficiently high (several times the estimated molecular weight between two adjacent entanglements) to determine the entanglement density from the rubbery plateau modulus, for which the method developed by S. Wu (J Polym Sci Part B: Polym Phys 1989, 27, 723–741) was applied. The entanglement density of flexibilized SMI proved to be about 20–25% higher than that of the nonflexibilized SMI. 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