TY - JOUR
T1 - One-pot synthesis of poly(ionic liquid)s with 1,2,3-triazolium-based backbones
T2 - Via clickable ionic liquid monomers
AU - Hirai, Ruka
AU - Hibino, Tatsuki
AU - Watanabe, Takaichi
AU - Teranishi, Takashi
AU - Ono, Tsutomu
N1 - Funding Information:
Financial support for this work was provided by the JSPS Grants-in-Aid for Scientic Research (KAKENHI) (Grant No. JP18H03854 and JP19K15340). We also acknowledge Prof. T. Uchida for the EDX measurements.
Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2020/10/13
Y1 - 2020/10/13
N2 - Clickable α-azide-ω-alkyne ionic liquid monomers were developed and subsequently applied to the one-pot synthesis of ionically conducting poly(ionic liquid)s with 1,2,3-triazolium-based backbones through a click chemistry strategy. This approach does not require the use of solvents, polymerisation mediators, or catalysts. The obtained poly(ionic liquid)s were characterized by NMR, differential scanning calorimetry, thermogravimetric analysis, and impedance spectroscopy analysis. Moreover, these poly(ionic liquid)s were cross-linked via N-alkylation with a dianion quarternizing agent to achieve enhanced ionic conductivity and mechanical strength. The resulting free-standing films showed a Young's modulus up to 4.8 MPa and ionic conductivities up to 4.60 × 10-8 S cm-1 at 30 °C. This facile synthetic strategy has the potential to expand the availability of poly(ionic liquid)s and promote the development of functional materials.
AB - Clickable α-azide-ω-alkyne ionic liquid monomers were developed and subsequently applied to the one-pot synthesis of ionically conducting poly(ionic liquid)s with 1,2,3-triazolium-based backbones through a click chemistry strategy. This approach does not require the use of solvents, polymerisation mediators, or catalysts. The obtained poly(ionic liquid)s were characterized by NMR, differential scanning calorimetry, thermogravimetric analysis, and impedance spectroscopy analysis. Moreover, these poly(ionic liquid)s were cross-linked via N-alkylation with a dianion quarternizing agent to achieve enhanced ionic conductivity and mechanical strength. The resulting free-standing films showed a Young's modulus up to 4.8 MPa and ionic conductivities up to 4.60 × 10-8 S cm-1 at 30 °C. This facile synthetic strategy has the potential to expand the availability of poly(ionic liquid)s and promote the development of functional materials.
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U2 - 10.1039/d0ra07948k
DO - 10.1039/d0ra07948k
M3 - Article
AN - SCOPUS:85094578058
SN - 2046-2069
VL - 10
SP - 37743
EP - 37748
JO - RSC Advances
JF - RSC Advances
IS - 62
ER -