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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Anion partitioning and ion-pairing behavior of anions in the extraction of cesium salts by 4,5 ''-bis(tert-octylbenzo)dibenzo-24-crown-8 in 1,2-dichloroethane
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Anion partitioning and ion-pairing behavior of anions in the extraction of cesium salts by 4,5 ''-bis(tert-octylbenzo)dibenzo-24-crown-8 in 1,2-dichloroethane

机译:1,5,2-二氯乙烷中4,5''-双(叔辛基苯并)二苯并-24-冠-8萃取铯盐中阴离子的阴离子分配和离子对行为

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A systematic study of anion partitioning and ion pairing was performed for an extraction of individual cesium salts into 1,2-dichloroethane (1,2-DCE) using 4,5 ''-bis(tert-octylbenzo)dibenzo-24-crown-8 as the cesium receptor. Equilibrium constants corresponding to the extraction of ion pairs and dissociated ions, formation of the 1:1 cesium/crown complex (confirmed by electrospray mass spectrometry), and dissociation of the ion pairs in water-saturated 1,2-DCE at 25 degrees C were obtained from equilibrium modeling using the SXLSQI program. The standard Gibbs energy of partitioning between water and water-saturated 1,2-DCE was determined for picrate, permanganate, trifluoromethanesulfonate, methanesulfonate, trifluoroacetate, and acetate anions. The dissociation of the organic-phase complex ion pair [Cs(4,4 ''-bis(tert-octylbenzo)dibenzo-24-crown-8)]+NO3- observed in the extraction experiments was shown to be consistent with the dissociation constant determined independently by conductance measurements. As attributed to the large effective radius of the complex cation, the evident anion discrimination due to ion pairing in the 1,2-DCE phase was relatively small, by comparison only a tenth of the discrimination exhibited by the anion partitioning. Only chloride and picrate exhibit evidence for significantly greater-than-expected ion-pairing tendency. These results provide insight into the inclusion properties of the clefts formed by opposing arene rings of the crown ether upon encapsulation of the Cs+ ion, whose weak anion recognition likely reflects the preferential inclusion of 1,2-DCE molecules in the clefts. Observed anion extraction selectivity in this system, which may be ascribed predominantly to solvent-induced Hofmeister bias selectivity toward large charge-diffuse anions, was nearly the same whether cesium salts were extracted as dissociated ions or ion pairs.
机译:进行了阴离子分配和离子对的系统研究,以使用4,5''-双(叔辛基苯并二苯)二苯并-24-皇冠-将单个铯盐萃取成1,2-二氯乙烷(1,2-DCE)。 8为铯受体。平衡常数,对应于离子对和解离离子的提取,1:1铯/冠状配合物的形成(通过电喷雾质谱法确认),以及25°C下水饱和的1,2-DCE中离子对的解离使用SXLSQI程序通过平衡建模获得。测定了苦味酸根,高锰酸根,三氟甲磺酸根,甲磺酸根,三氟乙酸根和乙酸根阴离子在水和水饱和的1,2-DCE之间分配的标准吉布斯能。萃取实验中观察到的有机相络合离子对[Cs(4,4''-双(叔辛基苯并)二苯并-24-皇冠-8)] + NO3-的解离与解离一致由电导测量值独立确定的常数。由于络合物阳离子的有效半径大,由1,2-DCE相中的离子对引起的明显的阴离子辨别力相对较小,相比之下,阴离子分配所表现出的辨别力只有十分之一。仅氯化物和苦味酸盐显示出明显大于预期的离子配对趋势的证据。这些结果提供了对囊封Cs +离子时冠醚的相对芳烃环形成的裂隙的包合特性的见解,其Cs +离子的弱阴离子识别能力可能反映了在裂隙中优先包含1,2-DCE分子。在该系统中观察到的阴离子萃取选择性(可能主要归因于溶剂诱导的对大电荷扩散阴离子的霍夫迈斯特偏压选择性),无论铯盐是作为离解离子还是离子对萃取的,几乎相同。

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