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
Тип публикации: Journal Article
Дата публикации: 2006-12-09
scimago Q1
wos Q1
БС1
SJR: 0.928
CiteScore: 7.6
Impact factor: 4.7
ISSN: 00201669, 1520510X
PubMed ID:
17198435
Inorganic Chemistry
Physical and Theoretical Chemistry
Краткое описание
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 °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.
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Levitskaia T. G. et al. 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 // Inorganic Chemistry. 2006. Vol. 46. No. 1. pp. 261-272.
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Levitskaia T. G., Maya L., Van Berkel G. J., Moyer B. 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 // Inorganic Chemistry. 2006. Vol. 46. No. 1. pp. 261-272.
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TY - JOUR
DO - 10.1021/ic061605k
UR - https://doi.org/10.1021/ic061605k
TI - 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
T2 - Inorganic Chemistry
AU - Levitskaia, Tatiana G.
AU - Maya, Leon
AU - Van Berkel, Gary J
AU - Moyer, Bruce
PY - 2006
DA - 2006/12/09
PB - American Chemical Society (ACS)
SP - 261-272
IS - 1
VL - 46
PMID - 17198435
SN - 0020-1669
SN - 1520-510X
ER -
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@article{2006_Levitskaia,
author = {Tatiana G. Levitskaia and Leon Maya and Gary J Van Berkel and Bruce Moyer},
title = {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},
journal = {Inorganic Chemistry},
year = {2006},
volume = {46},
publisher = {American Chemical Society (ACS)},
month = {dec},
url = {https://doi.org/10.1021/ic061605k},
number = {1},
pages = {261--272},
doi = {10.1021/ic061605k}
}
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MLA
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Levitskaia, Tatiana G., et al. “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.” Inorganic Chemistry, vol. 46, no. 1, Dec. 2006, pp. 261-272. https://doi.org/10.1021/ic061605k.