journal article·2022-03-11

Poly(ethylene glycol)-Based Poly(ionic liquid) Block Copolymers through 1,2,3-Triazole Click Reactions

Jukka Niskanen, Mathieu N. Tousignant, Alexander J. Peltekoff, Benoît H. Lessard

ACS Applied Polymer Materials· Volume 4· Issue 3
Publisher page

Abstract

1,2,3-Triazolium-based polyionic liquids (PILs) were made by a copper-catalyzed azide–alkyne cycloaddition (CuAAC) “click” reaction from poly(4-vinylbenzyl chloride). The click reaction facilitates the design and manipulation of the polymer architecture by selecting the desired alkynes, the azide-containing moieties, and the alkylating group of the 1,2,3-triazole group. Using this versatile chemistry and design, we prepared PILs with comblike homo- and block copolymer architectures using bistrifluoromethanesulfonimidate (TFSI-) as counterions. The block copolymer self-assembles into an ordered morphology. The block copolymer was integrated into metal–insulator–metal capacitors and found to display a prominent electrical double layer when characterized by electrochemical impedance spectroscopy.
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Research context

OpenAlex topics: Ionic liquids properties and applications · Organic Electronics and Photovoltaics · Advanced Polymer Synthesis and Characterization

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemical & Biological Engineering, University of Ottawa, 161 Louis Pasteur, Ottawa, Ontario K1N 6N5, Canada

VTT Technical Research Centre of Finland Ltd, P.O. Box 1000, Espoo FI-02044, Finland

School of Electrical Engineering and Computer Science, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada

Funding

Natural Sciences and Engineering Research Council of Canada

References (30)

Show source-provided references
1. 10.1002/adfm.20180220110.1002/adfm.201802201 ↗
2. 10.1039/C6CS00620E10.1039/C6CS00620E ↗
3. 10.1016/j.jpowsour.2016.03.04410.1016/j.jpowsour.2016.03.044 ↗
4. 10.3390/polym1206123110.3390/polym12061231 ↗
5. 10.1021/acsomega.9b0409810.1021/acsomega.9b04098 ↗
6. 10.1021/acs.macromol.7b0239410.1021/acs.macromol.7b02394 ↗
7. 10.1021/acsmacrolett.9b0007010.1021/acsmacrolett.9b00070 ↗
8. 10.1021/ma301036b10.1021/ma301036b ↗
9. 10.1021/ma400562a10.1021/ma400562a ↗
10. 10.1021/jacsau.1c0013310.1021/jacsau.1c00133 ↗
11. 10.1021/acsami.6b0197310.1021/acsami.6b01973 ↗
12. 10.1002/pola.2924210.1002/pola.29242 ↗
13. 10.1039/c2jm34270g10.1039/c2jm34270g ↗
14. 10.1039/C6PY02030E10.1039/C6PY02030E ↗
15. 10.1039/C9PY01923E10.1039/C9PY01923E ↗
16. 10.1016/j.polymer.2015.10.01010.1016/j.polymer.2015.10.010 ↗
17. 10.1016/j.polymer.2020.12314410.1016/j.polymer.2020.123144 ↗
18. 10.1016/j.eurpolymj.2014.08.02510.1016/j.eurpolymj.2014.08.025 ↗
19. 10.1039/C1RA00286D10.1039/C1RA00286D ↗
20. Yacob Z. · 2015 · 40 · 16710.1007/7081_2014_123 ↗
21. 10.1039/C5OB01457C10.1039/C5OB01457C ↗
22. 10.1021/ol402387w10.1021/ol402387w ↗
23. 10.1021/acsapm.9b0095910.1021/acsapm.9b00959 ↗
24. 10.1039/C6PY00937A10.1039/C6PY00937A ↗
25. 10.1021/ma201067h10.1021/ma201067h ↗
26. 10.1021/ma00240a03110.1021/ma00240a031 ↗
27. 10.1021/acsami.5b0049510.1021/acsami.5b00495 ↗
28. 10.1002/adfm.20090058810.1002/adfm.200900588 ↗
29. 10.1016/j.mser.2018.02.00410.1016/j.mser.2018.02.004 ↗
30. 10.1021/jp900037h10.1021/jp900037h ↗