Cargando…
Radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers
In this work, we synthesized end group functionalization of the cis-Norbornene-5-6-endo-dicarboxylic anhydride species via the ring-opening metathesis polymerization (ROMP) of oxanorbornene derivatives generated a chiseled poly(cis-Norbornene-5-6-endo-Dicarboxylic anhydride) acrylate macromonomer. F...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812107/ https://www.ncbi.nlm.nih.gov/pubmed/29491827 http://dx.doi.org/10.1080/15685551.2017.1409475 |
_version_ | 1783299979809390592 |
---|---|
author | Kollarigowda, Ravichandran H. Thakur, Pankaj |
author_facet | Kollarigowda, Ravichandran H. Thakur, Pankaj |
author_sort | Kollarigowda, Ravichandran H. |
collection | PubMed |
description | In this work, we synthesized end group functionalization of the cis-Norbornene-5-6-endo-dicarboxylic anhydride species via the ring-opening metathesis polymerization (ROMP) of oxanorbornene derivatives generated a chiseled poly(cis-Norbornene-5-6-endo-Dicarboxylic anhydride) acrylate macromonomer. Further, acrylate oxanorbornene based macromonomer further polymerized via reversible addition fragmentation chain transfer (RAFT) polymerization technique. Chain transfer is exhibited in the structure during the radical polymerizations so that free radical polymerization could also be used to comb structure copolymers with a PDI value below 1.2 with the help of acrylate oxanorbornene. Atomic force microscopy reveals the comb shape of branched polymer brushes structure. This method involves polymerizable end-group attachment to a macromonomer, and the backbone of the comb polymer is created in a second step of the polymerization. We believe that this kind of comb structured polymers can be considered for different biological applications. |
format | Online Article Text |
id | pubmed-5812107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-58121072018-02-28 Radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers Kollarigowda, Ravichandran H. Thakur, Pankaj Des Monomers Polym Original Articles In this work, we synthesized end group functionalization of the cis-Norbornene-5-6-endo-dicarboxylic anhydride species via the ring-opening metathesis polymerization (ROMP) of oxanorbornene derivatives generated a chiseled poly(cis-Norbornene-5-6-endo-Dicarboxylic anhydride) acrylate macromonomer. Further, acrylate oxanorbornene based macromonomer further polymerized via reversible addition fragmentation chain transfer (RAFT) polymerization technique. Chain transfer is exhibited in the structure during the radical polymerizations so that free radical polymerization could also be used to comb structure copolymers with a PDI value below 1.2 with the help of acrylate oxanorbornene. Atomic force microscopy reveals the comb shape of branched polymer brushes structure. This method involves polymerizable end-group attachment to a macromonomer, and the backbone of the comb polymer is created in a second step of the polymerization. We believe that this kind of comb structured polymers can be considered for different biological applications. Taylor & Francis 2017-12-05 /pmc/articles/PMC5812107/ /pubmed/29491827 http://dx.doi.org/10.1080/15685551.2017.1409475 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Kollarigowda, Ravichandran H. Thakur, Pankaj Radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers |
title | Radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers |
title_full | Radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers |
title_fullStr | Radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers |
title_full_unstemmed | Radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers |
title_short | Radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers |
title_sort | radical polymerization approach for ring opened oxanorbornene anhydride based macromonomers |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5812107/ https://www.ncbi.nlm.nih.gov/pubmed/29491827 http://dx.doi.org/10.1080/15685551.2017.1409475 |
work_keys_str_mv | AT kollarigowdaravichandranh radicalpolymerizationapproachforringopenedoxanorborneneanhydridebasedmacromonomers AT thakurpankaj radicalpolymerizationapproachforringopenedoxanorborneneanhydridebasedmacromonomers |