{"title":"SPECTROSCOPY STUDY OF MCl2(H2O)n CLUSTER USING AB INITIO CALCULATIONS","authors":"Ahmed M. Sadoon, O. S. Ahmad","doi":"10.52571/ptq.v17.n36.2020.599_periodico36_pgs_584_597.pdf","DOIUrl":null,"url":null,"abstract":"\nThe Infrared (IR) spectroscopy of alkali earth halide salt (MX2) complexes with few numbers of water molecules have been investigated for the first time in this work. BeCl2 and MgCl2 are divalent salts and have been incorporated with water as a polar solvent to form complexes of type MX2(H2O)n. The effect of ion size plays a critical rule in the interactions between solvent and solute. Therefore, Beryllium and Magnesium salts with chloride were chosen to explore this difference. The importance of BeCl2 and MgCl2 comes from their several applications in the industry and pharmacy. For instance, BeCl2 is widely used in the industry as a catalysis of Friede-Craft reactions, while the main application of MgCl2 in pharmacy is as hemodialysis and peritoneal dialysis fluids. Three complexes of each BeCl2 and MgCl2 with water, MX2(H2O)n (n=1-3), were studied, and the chemical structures of these complexes have been performed using ab initio calculations. Ab initio calculations were used to predict possible structures, isomers, and their corresponding IR spectra using Second-order Møller-Plesset perturbation theory (MP2) with 6-311++G as a basis sets. The Geometry evaluations, energy searches, vibrational frequency calculations, and the binding energy of each complex were also extracted theoretically. The minimum energy of complexes structures was calculated, and different isomers have been recorded. Ionic hydrogen bonds (IHBs) between the OH in each water molecule and the chloride ion in the MCl2 was proposed to be the main prevalent contribution to the binding between the salt and water. The bond length between the alkaline metal and chlorine showed a significant increase with increasing the attached water molecule as a result of forming the IHB. Also, the infrared vibrational bands of the OH stretching region were recorded for the minimum structures, and dramatic redshift was performed. The formation of contact-ion pair structures in which each solvent molecule forms an ionic hydrogen bond (IHB) to the salt ion-pair (X-M+X-) has been confirmed by the predicted infrared spectra.\n","PeriodicalId":45103,"journal":{"name":"Periodico Tche Quimica","volume":" ","pages":""},"PeriodicalIF":0.2000,"publicationDate":"2020-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Periodico Tche Quimica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.52571/ptq.v17.n36.2020.599_periodico36_pgs_584_597.pdf","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The Infrared (IR) spectroscopy of alkali earth halide salt (MX2) complexes with few numbers of water molecules have been investigated for the first time in this work. BeCl2 and MgCl2 are divalent salts and have been incorporated with water as a polar solvent to form complexes of type MX2(H2O)n. The effect of ion size plays a critical rule in the interactions between solvent and solute. Therefore, Beryllium and Magnesium salts with chloride were chosen to explore this difference. The importance of BeCl2 and MgCl2 comes from their several applications in the industry and pharmacy. For instance, BeCl2 is widely used in the industry as a catalysis of Friede-Craft reactions, while the main application of MgCl2 in pharmacy is as hemodialysis and peritoneal dialysis fluids. Three complexes of each BeCl2 and MgCl2 with water, MX2(H2O)n (n=1-3), were studied, and the chemical structures of these complexes have been performed using ab initio calculations. Ab initio calculations were used to predict possible structures, isomers, and their corresponding IR spectra using Second-order Møller-Plesset perturbation theory (MP2) with 6-311++G as a basis sets. The Geometry evaluations, energy searches, vibrational frequency calculations, and the binding energy of each complex were also extracted theoretically. The minimum energy of complexes structures was calculated, and different isomers have been recorded. Ionic hydrogen bonds (IHBs) between the OH in each water molecule and the chloride ion in the MCl2 was proposed to be the main prevalent contribution to the binding between the salt and water. The bond length between the alkaline metal and chlorine showed a significant increase with increasing the attached water molecule as a result of forming the IHB. Also, the infrared vibrational bands of the OH stretching region were recorded for the minimum structures, and dramatic redshift was performed. The formation of contact-ion pair structures in which each solvent molecule forms an ionic hydrogen bond (IHB) to the salt ion-pair (X-M+X-) has been confirmed by the predicted infrared spectra.
本文首次研究了含少量水分子的碱土卤化物配合物的红外光谱。BeCl2和MgCl2是二价盐,作为极性溶剂与水结合形成MX2(H2O)n型配合物。离子大小的影响在溶剂与溶质的相互作用中起着至关重要的作用。因此,选择含氯的铍盐和镁盐来探索这种差异。BeCl2和MgCl2的重要性来自于它们在工业和制药中的一些应用。例如,BeCl2作为Friede-Craft反应的催化剂在工业上被广泛使用,而MgCl2在药学上的主要应用是作为血液透析和腹膜透析液。本文研究了BeCl2和MgCl2与水的配合物MX2(H2O)n (n=1-3),并用从头算法计算了配合物的化学结构。以6-311++G为基集,采用二阶Møller-Plesset微扰理论(MP2)从头计算,预测了可能的结构、异构体及其相应的红外光谱。从理论上提取了每个配合物的几何评价、能量搜索、振动频率计算和结合能。计算了配合物结构的最小能量,并记录了不同的异构体。离子氢键(IHBs)在每个水分子中的OH和MCl2中的氯离子之间被认为是盐和水之间结合的主要普遍贡献。碱金属与氯之间的键长随着水分子的增加而显著增加。同时记录了最小结构的氢氧根拉伸区红外振动带,并发生了明显的红移。预测的红外光谱证实了溶剂分子与盐离子对(X- m +X-)形成离子氢键(IHB)的接触离子对结构的形成。
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