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Highly Stable N3-Substituted Imidazolium-Based Alkaline Anion Exchange Membranes: Experimental Studies and Theoretical Calculations

Gu, Fenglou, Dong, Huilong, Li, Youyong, Si, Zhihong, Yan, Feng·2014·Macromolecules

Abstract

Imidazolium cations with various N3-substituents (including methyl, butyl, heptyl, dodecyl, isopropyl, and diphenylmethyl groups) were synthesized and investigated in terms of their alkaline stability. The effect of the N3-substituent on the alkaline stability was studied by quantitative 1 H NMR spectra and density functional theory (GGA-BLYP) calculations. The isopropyl substituted imidazolium cation ([DMIIm] + ) with the highest LUMO energy value exhibited the highest alkaline stability in aqueous NaOH. The [DMIIm] + cation also exhibited higher alkaline stability than that of a quaternary ammonium cation, benzyltrimethyl-ammonium ([BTMA] + ), in CD 3 OD/D 2 O NaOH solution at elevated temperatures. This observation inspired the preparation of [DMIIm] + -based alkaline anion exchange membranes (AEMs) which showed high alkaline stability in alkaline solution.

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Metadata

Authors
Gu, F., Dong, H., Li, Y., Si, Z., & Yan, F.
Venue
Macromolecules
Published
2013-12-19
Volume
47
Issue
1
Pages
208-216
ISSN
  • 0024-9297 (ISSN-L)
  • 1520-5835
OpenAlex
W2333560421
Cited by
173
References
2
FWCI
8.79
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Highly Stable N3-Substituted Imidazolium-Based Alkaline Anion Exchange Membranes: Experimental Studies and Theoretical Calculations. https://app.cochat.ai/papers/10.1021/ma402334t
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Gu, F., Dong, H., Li, Y., Si, Z., & Yan, F. (2014). Highly Stable N3-Substituted Imidazolium-Based Alkaline Anion Exchange Membranes: Experimental Studies and Theoretical Calculations. Macromolecules. https://doi.org/10.1021/ma402334t

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