1, 2, 3‐Triazolium‐Based Poly(ionic liquid)s Obtained Through Click Chemistry Polyaddition. Issue 22 (10th June 2014)
- Record Type:
- Journal Article
- Title:
- 1, 2, 3‐Triazolium‐Based Poly(ionic liquid)s Obtained Through Click Chemistry Polyaddition. Issue 22 (10th June 2014)
- Main Title:
- 1, 2, 3‐Triazolium‐Based Poly(ionic liquid)s Obtained Through Click Chemistry Polyaddition
- Authors:
- Abdelhedi‐Miladi, Imen
Obadia, Mona M.
Allaoua, Imène
Serghei, Anatoli
Romdhane, Hatem Ben
Drockenmuller, Eric
Meier, Michael
Dove, Andrew - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>A series of four 1, 2, 3‐triazolium‐based poly(ionic liquid)s (TPILs) is synthesized from the polyaddition of different tailor‐made α‐azide‐ω‐alkyne monomers by copper(I)‐catalyzed azide–alkyne cycloaddition (CuAAC), followed by quaternization with methyl iodide and subsequent anion exchange with lithium bis(trifluoromethylsulfonyl)imide. Whereas the chemical structures of the bis(trifluoromethylsulfonyl)imide counter anion and the <italic>N</italic>‐3 methyl group are common to all TPILs, the structural features of the repeating units, i.e., triethylene glycol or undecanoyl spacers with either ester or ether linkages, are varied and compared. Their impact on the physical and ion‐conducting properties of the obtained TPILs is established based on <sup>1</sup>H NMR, DSC, thermogravimetric analysis (TGA), and broadband dielectric spectroscopy (BDS) characterization techniques. Most importantly, the replacement of an ether by an ester group at the <italic>C</italic>‐4 position of the 1, 2, 3‐triazolium ring significantly decreases the thermal stability and ionic conductivity of TPILs, whereas the chemical nature of the triethylene glycol or undecanoyl spacers has little influence on the materials properties. <boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgh2cmsm3hf"<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>A series of four 1, 2, 3‐triazolium‐based poly(ionic liquid)s (TPILs) is synthesized from the polyaddition of different tailor‐made α‐azide‐ω‐alkyne monomers by copper(I)‐catalyzed azide–alkyne cycloaddition (CuAAC), followed by quaternization with methyl iodide and subsequent anion exchange with lithium bis(trifluoromethylsulfonyl)imide. Whereas the chemical structures of the bis(trifluoromethylsulfonyl)imide counter anion and the <italic>N</italic>‐3 methyl group are common to all TPILs, the structural features of the repeating units, i.e., triethylene glycol or undecanoyl spacers with either ester or ether linkages, are varied and compared. Their impact on the physical and ion‐conducting properties of the obtained TPILs is established based on <sup>1</sup>H NMR, DSC, thermogravimetric analysis (TGA), and broadband dielectric spectroscopy (BDS) characterization techniques. Most importantly, the replacement of an ether by an ester group at the <italic>C</italic>‐4 position of the 1, 2, 3‐triazolium ring significantly decreases the thermal stability and ionic conductivity of TPILs, whereas the chemical nature of the triethylene glycol or undecanoyl spacers has little influence on the materials properties. <boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgh2cmsm3hf" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></boxed-text></p> </abstract> … (more)
- Is Part Of:
- Macromolecular chemistry and physics. Volume 215:Issue 22(2014:Nov.)
- Journal:
- Macromolecular chemistry and physics
- Issue:
- Volume 215:Issue 22(2014:Nov.)
- Issue Display:
- Volume 215, Issue 22 (2014)
- Year:
- 2014
- Volume:
- 215
- Issue:
- 22
- Issue Sort Value:
- 2014-0215-0022-0000
- Page Start:
- 2229
- Page End:
- 2236
- Publication Date:
- 2014-06-10
- Subjects:
- Polymers -- Periodicals
Polymerization -- Periodicals
Synthetic products -- Periodicals
Macromolecules -- Periodicals
547.7 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3935 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/macp.201400182 ↗
- Languages:
- English
- ISSNs:
- 1022-1352
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5330.398000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3882.xml