Vieira Jean C B, Villetti Marcos A, Bender Caroline R, Frizzo Clarissa P
NUQUIMHE, Department of Chemistry, Federal University of Santa Maria, Santa Maria 97105-900, Brazil.
LEPOL, Department of Physics, Federal University of Santa Maria, Santa Maria 97105-900, Brazil.
ACS Omega. 2025 Feb 26;10(9):9514-9526. doi: 10.1021/acsomega.4c10596. eCollection 2025 Mar 11.
This work presents the synthesis of mono- and dicationic ionic liquids (ILs) that combine the cations 1-butyl-3-methylimidazolium ([CMIM]), 1-decyl-3-methylimidazolium ([CMIM]), 1,4-bis(3-methylimidazolium-1-yl)butane ([C(MIM)]), and 1,10-bis(3-methylimidazolium-1-yl)decane ([C(MIM)]) with the anion dodecanoate ([CCOO]), along with a study into their thermal stability and mechanism for thermal decomposition. Thermal stability was investigated using the Kissinger-Akahira-Sunose (KAS) isoconversional method to determine the isoconversional activation energies (E ) and compensation effect to calculate the pre-exponential factor (ln ). The results showed that there was no significant difference in the thermal stabilities between the ILs, with all compounds being thermally stable up to 450 K. The thermal decomposition mechanism was analyzed using nuclear magnetic resonance (NMR), electrospray ionization mass spectrometry (ESI-MS), and thermogravimetric analysis coupled with Fourier-transform infrared spectroscopy (TGA-FTIR). The main decomposition pathways were nucleophilic substitution at the lateral or spacer chain and the methyl group.
这项工作展示了单阳离子和双阳离子离子液体(ILs)的合成,这些离子液体将阳离子1-丁基-3-甲基咪唑鎓([CMIM])、1-癸基-3-甲基咪唑鎓([CMIM])、1,4-双(3-甲基咪唑鎓-1-基)丁烷([C(MIM)])和1,10-双(3-甲基咪唑鎓-1-基)癸烷([C(MIM)])与阴离子十二烷酸根([CCOO])相结合,同时还对它们的热稳定性及其热分解机理进行了研究。使用基辛格-赤平-ose(KAS)等转化率方法研究热稳定性,以确定等转化率活化能(E )并通过补偿效应计算指前因子(ln )。结果表明,离子液体之间的热稳定性没有显著差异,所有化合物在高达450 K时都是热稳定的。使用核磁共振(NMR)、电喷雾电离质谱(ESI-MS)以及热重分析与傅里叶变换红外光谱联用(TGA-FTIR)对热分解机理进行了分析。主要分解途径是在侧链或间隔链以及甲基处的亲核取代。