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581.
Evaluating the solvation properties of functionalized ionic liquids with varied cation/anion composition using the solvation parameter model 总被引:1,自引:0,他引:1
Twu P Zhao Q Pitner WR Acree WE Baker GA Anderson JL 《Journal of chromatography. A》2011,1218(31):5311-5318
Ionic liquids (ILs) are promising gas chromatography (GC) stationary phases due to their high thermal stability, negligible vapor pressure, and ability to solvate a broad range of analytes. The tunability of ILs allows for structure modification in pursuit of enhanced separation selectivity and control of analyte elution order. In this study, the solvation parameter model is used to characterize the solvation interactions of fifteen ILs containing various cationic functional groups (i.e., dimethylamino, hydroxyl, and ether) and cation types paired with various counter anions, namely, tris(pentafluoroethyl)trifluorophosphate (FAP(-)), bis[(trifluoromethyl)sulfonyl]imide (NTf(2)(-)), thiocyanate (SCN(-)), tricyanomethide (C(CN)(3)(-)), tetracyanoborate (B(CN)(4)(-)), and bis[oxalate(2-)]borate (BOB(-)). The presence of functional groups affected the hydrogen bond basicity, hydrogen bond acidity, as well as dispersion interactions of the resulting ILs, while the change of cation type yielded modest influence on the dipolarity. The switch of counter anions in unfunctionalized ILs produced compounds with higher dipolarity and hydrogen bond basicity. The dipolarity and hydrogen bond basicity of ILs possessing cyano-containing anions appeared to be inversely proportional to the cyano content of the anion. The modification of IL structure resulted in a significant effect on the retention behavior as well as separation selectivity for many solutes, including reversed elution orders of some analytes. This study provides one of the most comprehensive examinations up-to-date on the relation between IL structure and the resulting solvation characteristics and gives tremendous insight into choosing suitable ILs as GC stationary phases for solute specific separations. 相似文献
582.
Lijuan J. Wang Margaret L. Grapperhaus Barnett S. Pitzele Timothy J. Hagen Kam F. Fok Jeffrey A. Scholten Dale P. Spangler Mihaly V. Toth Gina M. Jerome William M. Moore Pamela T. Manning James A. Sikorski 《Heteroatom Chemistry》2002,13(1):77-83
The efficient syntheses of two new types of conformationally constrained S‐[2‐[(1‐iminoethyl)amino]ethyl]homocysteine derivatives, 1‐amino‐3‐[2[(1‐iminoethyl)amino]ethylthio]cyclobutane carboxylic Acid ( 5 ) and (4S)‐4‐[[2‐[(1‐Iminoethyl)amino]ethyl]thio]‐L‐proline ( 6 ), are reported. These molecules represent the first attempts to probe conformational constraint near the α‐amino acid moiety of known homocysteine‐based inhibitors of nitric oxide synthase. Targets 5 and 6 were evaluated as potential inhibitors of the three human isoforms of nitric oxide synthase. © 2002 John Wiley & Sons, Inc. Heteroatom Chem 13:77–83, 2002; DOI 10.1002/hc.1109 相似文献
583.
Po-Hsiang Tang Pamela Berilyn So Zi-Jing Lin Chia-Chun Hsieh Lee-Jene Lai Chia-Her Lin 《中国化学会会志》2023,70(5):1108-1115
This paper mainly discusses the applicability of using soft x-ray tomography technology to examine the multidimensional structure of metal–organic frameworks, such as their core-shell and hollow framework, by visually observing their corresponding images in different energy bands by different excitation energies for different elements. The results show that the use of soft x-ray tomography (SXT) can effectively observe the distribution of metals in the structure, as well as observe the type of hollow pores the metal – organic framework (MOF) possesses. This pioneering evaluation of MOFs via SXT shows excellent performance in the structure identification of multidimensional metal–organic frameworks. 相似文献
584.
Christelle Miola‐Delaite Erwan Colomb Eric Pollet Thierry Hamaide 《Macromolecular Symposia》2000,153(1):275-286
585.
The metastable 1:1 Li/Na-stacked OP4-Li0.42Na0.37CoO2 phase is synthesized from a mixture of O3-LiCoO2 and P2-Na0.7CoO2 in a molar ratio of 42:58 (sealed gold tubes, 920 °C, 24 h, very fast quenching). 相似文献