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New organic ionic plastic crystals based on pyrrolidinium dication for a solid-phase electrolyte

Authors
Shin, JC[Shin, Jong Chan]Kim, TY[Kim, Tae Young]Kim, HJ[Kim, Hwi Jung]Choi, UH[Choi, U. Hyeok]Park, HS[Park, Ho Seok]Lee, M[Lee, Minjae]
Issue Date
Apr-2023
Publisher
WILEY-V C H VERLAG GMBH
Keywords
bis-pyrrolidnium; dicationic salt; organic ionic plastic crystals; solid electrolyte; solid-solid phase transition; solid-state morphology
Citation
BULLETIN OF THE KOREAN CHEMICAL SOCIETY, v.44, no.4, pp.310 - 321
Indexed
SCIE
SCOPUS
KCI
Journal Title
BULLETIN OF THE KOREAN CHEMICAL SOCIETY
Volume
44
Number
4
Start Page
310
End Page
321
URI
https://scholarworks.bwise.kr/skku/handle/2021.sw.skku/102439
DOI
10.1002/bkcs.12668
ISSN
0253-2964
Abstract
A series of 1,4-bis(N-alkylpyrrolidinium)butane salts combined with Br-, I-, PF6-, and Tf2N- anions were newly designed and synthesized. In nonpolar CDCl3 solution, the axial and equatorial proton peaks of the bis-pyrrolidinium cation ring are distinguished in H-1 NMR. Also, the strengths of ion paring could be estimated from the H-1 NMR chemical shift changes of the bridge and pyrrolidinium proton peaks. 1,4-Bis(N-hepthylpyrrolidinium)butane I- is an organic ionic plastic crystal showing the lowest fusion entropy value (delta S-f = 3.4 J Kmiddotmol(-1)). Softer crystalline morphologies were found by polarized optical microscope images at plastic crystal phase of each sample and the results were corresponding to differential scanning calorimetry results. 1,4-Bis(N-ethylpyrrolidinium)butane Tf2N- showed the softest crystal phase. Ionic conductivity changes and electrochemical stabilities of the bis-pyrrolidinium PF6- and Tf2N- salts were also measured, and they were stable up to 4.3 V (vs. Li/Li+) and expected to be applied as an electrolyte component.
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