Hirai Ruka, Hibino Tatsuki, Watanabe Takaichi, Teranishi Takashi, Ono Tsutomu
Department of Applied Chemistry, Graduate School of Natural Science, Okayama University 3-1-1, Tsushima-naka, Kita-ku Okayama 700-8530 Japan
RSC Adv. 2020 Oct 13;10(62):37743-37748. doi: 10.1039/d0ra07948k. eCollection 2020 Oct 12.
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 -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 S cm 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.
可点击的α-叠氮基-ω-炔基离子液体单体被开发出来,随后通过点击化学策略应用于一锅法合成具有1,2,3-三唑鎓基主链的离子导电聚(离子液体)。这种方法不需要使用溶剂、聚合介质或催化剂。通过核磁共振、差示扫描量热法、热重分析和阻抗谱分析对所得的聚(离子液体)进行了表征。此外,这些聚(离子液体)与二阴离子季铵化剂进行交联烷基化反应,以提高离子电导率和机械强度。所得的自支撑膜在30°C时的杨氏模量高达4.8MPa,离子电导率高达4.60×10 S cm。这种简便的合成策略有潜力扩大聚(离子液体)的可用性,并促进功能材料的发展。