Kabita Boruah , Shahnaz Rohman , Ankur K. Guha , Sukanya Das , Ruli Borah
{"title":"n -磺酸功能化环铵基Brӧnsted酸性离子液体在分子溶剂中的物理和电化学行为研究","authors":"Kabita Boruah , Shahnaz Rohman , Ankur K. Guha , Sukanya Das , Ruli Borah","doi":"10.1016/j.jil.2023.100062","DOIUrl":null,"url":null,"abstract":"<div><p>Two types of six Brӧnsted acidic ionic liquids of N-SO<sub>3</sub>H tethered cyclic ammonium cations (five, six and seven membered) with four anions namely [AcO]<sup>−</sup>, [HSO<sub>4</sub>]<sup>−</sup>, [BF<sub>4</sub>]<sup>−</sup>, [PF<sub>6</sub>]<sup>−</sup> were synthesized to evaluate their physical and electrochemical behavior in polar solvents (water, MeOH & CH<sub>3</sub>CN) using conductivity and Cyclic Voltammetry techniques. Their comparative Brönsted acidic orders were determined using UV–visible Hammett plots. Except the ionic liquid of [PF<sub>6</sub>]<sup>−</sup> anion with N,N-disulfopiperidinium cation, the thermal stabilities of other ionic liquids found within 230–250 °C. Solvent dependent aggregative nature was observed in polar solvents for the ionic liquids at a particular temperature and concentration. Their aggregative properties were also evidenced by comparison of experimental and computed chemical shift values of additional acidic protons of <sup>1</sup>H NMR spectra. Kamlet-Taft solvatochromic parameters of molecular solvents (E<sub>T</sub><sup>N</sup>, α, β) were correlated with their observed conductivities. Piperidinium ionic liquids showed wider electrochemical windows (2.99 V to 2.55 V) in acetonitrile as compared to other cyclic ammonium ionic liquids in polar solvents.</p></div>","PeriodicalId":100794,"journal":{"name":"Journal of Ionic Liquids","volume":"3 2","pages":"Article 100062"},"PeriodicalIF":0.0000,"publicationDate":"2023-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Investigation of physical and electrochemical behaviour of N-sulfonic acid functionalized cyclic-ammonium based Brӧnsted acidic ionic liquids in molecular solvents\",\"authors\":\"Kabita Boruah , Shahnaz Rohman , Ankur K. Guha , Sukanya Das , Ruli Borah\",\"doi\":\"10.1016/j.jil.2023.100062\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Two types of six Brӧnsted acidic ionic liquids of N-SO<sub>3</sub>H tethered cyclic ammonium cations (five, six and seven membered) with four anions namely [AcO]<sup>−</sup>, [HSO<sub>4</sub>]<sup>−</sup>, [BF<sub>4</sub>]<sup>−</sup>, [PF<sub>6</sub>]<sup>−</sup> were synthesized to evaluate their physical and electrochemical behavior in polar solvents (water, MeOH & CH<sub>3</sub>CN) using conductivity and Cyclic Voltammetry techniques. Their comparative Brönsted acidic orders were determined using UV–visible Hammett plots. Except the ionic liquid of [PF<sub>6</sub>]<sup>−</sup> anion with N,N-disulfopiperidinium cation, the thermal stabilities of other ionic liquids found within 230–250 °C. Solvent dependent aggregative nature was observed in polar solvents for the ionic liquids at a particular temperature and concentration. Their aggregative properties were also evidenced by comparison of experimental and computed chemical shift values of additional acidic protons of <sup>1</sup>H NMR spectra. Kamlet-Taft solvatochromic parameters of molecular solvents (E<sub>T</sub><sup>N</sup>, α, β) were correlated with their observed conductivities. Piperidinium ionic liquids showed wider electrochemical windows (2.99 V to 2.55 V) in acetonitrile as compared to other cyclic ammonium ionic liquids in polar solvents.</p></div>\",\"PeriodicalId\":100794,\"journal\":{\"name\":\"Journal of Ionic Liquids\",\"volume\":\"3 2\",\"pages\":\"Article 100062\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Ionic Liquids\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772422023000149\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Ionic Liquids","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772422023000149","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Investigation of physical and electrochemical behaviour of N-sulfonic acid functionalized cyclic-ammonium based Brӧnsted acidic ionic liquids in molecular solvents
Two types of six Brӧnsted acidic ionic liquids of N-SO3H tethered cyclic ammonium cations (five, six and seven membered) with four anions namely [AcO]−, [HSO4]−, [BF4]−, [PF6]− were synthesized to evaluate their physical and electrochemical behavior in polar solvents (water, MeOH & CH3CN) using conductivity and Cyclic Voltammetry techniques. Their comparative Brönsted acidic orders were determined using UV–visible Hammett plots. Except the ionic liquid of [PF6]− anion with N,N-disulfopiperidinium cation, the thermal stabilities of other ionic liquids found within 230–250 °C. Solvent dependent aggregative nature was observed in polar solvents for the ionic liquids at a particular temperature and concentration. Their aggregative properties were also evidenced by comparison of experimental and computed chemical shift values of additional acidic protons of 1H NMR spectra. Kamlet-Taft solvatochromic parameters of molecular solvents (ETN, α, β) were correlated with their observed conductivities. Piperidinium ionic liquids showed wider electrochemical windows (2.99 V to 2.55 V) in acetonitrile as compared to other cyclic ammonium ionic liquids in polar solvents.