CO2 capturing by self-assembled belt[14]pyridine encapsulated ionic liquid complexes: a DFT study†

IF 3.9 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2024-10-08 DOI:10.1039/D4RA03394A
Annum Ahsan, Ahmed Lakhani, Muhammad Umair Ashraf, Muhammad Yar, Sehrish Sarfaraz and Khurshid Ayub
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Abstract

In the current study, CO2 capturing ability of encapsulated ionic liquids (ENILs) i.e., tetramethylammonium chloride (TMACl), 1,3-dimethylimidazolium chloride (MIMCl), and methylpyridinium hexafluorophosphate (MPHP) encapsulated in self assembled belt[14]pyridine (BP) has been studied. The results show that strong van der Waals forces are involved in capturing of CO2 by these encapsulated ionic liquids. Strong attractive forces arise from synergistic effect of ionic liquid (encapsulated) and atoms of belt. The interaction energies (Eint) ranging from −12.54 to −18.64 kcal mol−1 reveal the capturing of CO2 by these systems as thermodynamically feasible process. The type and strength of interactions between CO2 and encapsulated ionic liquids is studied through QTAIM and NCI analyses. NCI analysis clearly shows that capturing of CO2 is assisted by van der Waals forces between CO2 and encapsulated ionic liquid complexes. The same feature is confirmed through QTAIM analysis as well. Natural bond orbital (NBO) analysis' results show the charge transfer between the fragments (encapsulated ionic liquids and CO2) which is validated further through electron density differences (EDD) analysis. Overall, transfer of charge towards CO2 from encapsulated ionic liquids is proved through the charge accumulation over CO2 (i.e., blue isosurfaces on CO2 molecules) through EDD analysis. The FMO analyses show the decrease in H–L gaps of encapsulated ionic liquids after CO2 capturing. The successful charge transfer and reduction in H–L gap indicate better interaction in the designed systems thus revealing these systems as a potential candidates for CO2 capturing. Overall, the best results for CO2 capture i.e., the highest interaction energy, the lowest H–L gap, and the strongest forces of interactions are shown by methylpyridinium hexafluorophosphate (MPHP) encapsulated belt[14]pyridine (BP–MPHP) system. This is due to the larger anion of methylpyridinium hexafluorophosphate as compared to the other two encapsulated ionic liquids with Cl as anion which enables it to develop strong interactions with CO2. The designed belt[14]pyridine based encapsulated ionic liquid systems are promising prospects with better CO2 capture performance and represent a new entrant in the CO2 capturing systems.

Abstract Image

自组装带[14]吡啶封装离子液体复合物捕获二氧化碳:DFT 研究。
本研究对封装在自组装带[14]吡啶(BP)中的封装离子液体(ENILs),即四甲基氯化铵(TMACl)、1,3-二甲基氯化咪唑(MIMCl)和六氟磷酸甲基吡啶(MPHP)的二氧化碳捕获能力进行了研究。研究结果表明,这些封装离子液体在捕获二氧化碳时会产生强大的范德华力。离子液体(封装)和传送带原子的协同效应产生了强大的吸引力。相互作用能(E int)从 -12.54 到 -18.64 kcal mol-1 不等,表明这些系统捕获二氧化碳的过程在热力学上是可行的。通过 QTAIM 和 NCI 分析,研究了二氧化碳与封装离子液体之间相互作用的类型和强度。NCI 分析清楚地表明,二氧化碳和封装离子液体复合物之间的范德华力有助于捕获二氧化碳。QTAIM 分析也证实了这一特征。自然键轨道(NBO)分析结果显示了碎片(封装离子液体和二氧化碳)之间的电荷转移,电子密度差(EDD)分析进一步验证了这一点。总体而言,电荷从封装离子液体向二氧化碳的转移是通过二氧化碳上的电荷积累(即二氧化碳分子上的蓝色等表面)来证明的。FMO 分析表明,捕获二氧化碳后,封装离子液体的 H-L 间隙减小。成功的电荷转移和 H-L 间隙的减小表明所设计的系统具有更好的相互作用,从而揭示了这些系统具有捕获二氧化碳的潜力。总体而言,六氟磷酸甲基吡啶鎓(MPHP)包裹带[14]吡啶(BP-MPHP)体系的二氧化碳捕获效果最好,即相互作用能量最高、H-L 间隙最小、相互作用力最强。这是由于六氟磷酸甲基吡啶鎓的阴离子比以 Cl- 为阴离子的其他两种封装离子液体的阴离子大,这使其能够与二氧化碳产生强烈的相互作用。所设计的基于带[14]吡啶的封装离子液体系统前景广阔,具有更好的二氧化碳捕获性能,是二氧化碳捕获系统的新成员。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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