Vinylimidazole‐based asymmetric ion pair comonomers: Synthesis, polymerization studies and formation of ionically crosslinked PMMA. Issue 15 (15th May 2013)
- Record Type:
- Journal Article
- Title:
- Vinylimidazole‐based asymmetric ion pair comonomers: Synthesis, polymerization studies and formation of ionically crosslinked PMMA. Issue 15 (15th May 2013)
- Main Title:
- Vinylimidazole‐based asymmetric ion pair comonomers: Synthesis, polymerization studies and formation of ionically crosslinked PMMA
- Authors:
- Jana, Satyasankar
Vasantha, Vivek Arjunan
Stubbs, Ludger Paul
Parthiban, Anbanandam
Vancso, Julius G. - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>Vinylimidazole‐based asymmetric ion pair comonomers (<bold>IPC</bold>s) which are free from nonpolymerizable counter ions have been synthesized, characterized and polymerized by free radical polymerization (FRP), atom transfer radical polymerization (ATRP), and reversible addition‐fragmentation chain transfer (RAFT) mediated polymerizations in solution and by dispersion polymerization in water. The asymmetric nature of <bold>IPC</bold>s is due to the fact that cationic component of these <bold>IPCs</bold> is derived from vinylimidazole (VIm) and anionic component is derived from either styrenesulfonate (SS) or 2‐acrylamido‐2‐methyl‐1‐propanesulfonate. Although under ATRP, conversions are either very low or negligible, FRP and RAFT produces polymers with high to moderate monomer conversions but with different solubility characteristics. This investigation provides insight to the polymerization behavior of each component of the asymmetric <bold>IPCs</bold> and also its effects on composition and solubility characteristics of the resulting polymers. The <bold>IPCs</bold> studied here are high temperature ionic liquid and thus the polymers synthesized from these <bold>IPCs</bold> are highly ionic in nature and possess very strong intermolecular interactions which makes some of these <bold>IPC</bold> based polymers completely insoluble in organic and aqueous solvents. This highly ionic interaction is exploited to<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Vinylimidazole‐based asymmetric ion pair comonomers (<bold>IPC</bold>s) which are free from nonpolymerizable counter ions have been synthesized, characterized and polymerized by free radical polymerization (FRP), atom transfer radical polymerization (ATRP), and reversible addition‐fragmentation chain transfer (RAFT) mediated polymerizations in solution and by dispersion polymerization in water. The asymmetric nature of <bold>IPC</bold>s is due to the fact that cationic component of these <bold>IPCs</bold> is derived from vinylimidazole (VIm) and anionic component is derived from either styrenesulfonate (SS) or 2‐acrylamido‐2‐methyl‐1‐propanesulfonate. Although under ATRP, conversions are either very low or negligible, FRP and RAFT produces polymers with high to moderate monomer conversions but with different solubility characteristics. This investigation provides insight to the polymerization behavior of each component of the asymmetric <bold>IPCs</bold> and also its effects on composition and solubility characteristics of the resulting polymers. The <bold>IPCs</bold> studied here are high temperature ionic liquid and thus the polymers synthesized from these <bold>IPCs</bold> are highly ionic in nature and possess very strong intermolecular interactions which makes some of these <bold>IPC</bold> based polymers completely insoluble in organic and aqueous solvents. This highly ionic interaction is exploited to synthesize ionically crosslinked PMMA. MMA on copolymerization with 5–6 mol % of <bold>IPC</bold> yielded copolymer which is insoluble in common organic solvents like THF, DMF, etc., unlike homo PMMA. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 3260–3273</p> </abstract> … (more)
- Is Part Of:
- Journal of polymer science. Volume 51:Issue 15(2013:Aug.)
- Journal:
- Journal of polymer science
- Issue:
- Volume 51:Issue 15(2013:Aug.)
- Issue Display:
- Volume 51, Issue 15 (2013)
- Year:
- 2013
- Volume:
- 51
- Issue:
- 15
- Issue Sort Value:
- 2013-0051-0015-0000
- Page Start:
- 3260
- Page End:
- 3273
- Publication Date:
- 2013-05-15
- Subjects:
- 547
- Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1099-0518 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pola.26720 ↗
- Languages:
- English
- ISSNs:
- 0887-624X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5041.002050
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3509.xml