Calixarene HPLC phases - Applications

被引:37
作者
Meyer, Ruediger [1 ]
Jira, Thomas [1 ]
机构
[1] Ernst Moritz Arndt Univ Greifswald, Inst Pharm Pharmaceut Med Chem, FL Jahn Str 17, D-17489 Greifswald, Germany
关键词
calixarene-bonded stationary phases; HPLC;
D O I
10.2174/157341107780361736
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Calixarenes, following cyclodextrines and crown ethers, are the third generation of supramolecules used in HPLC as stationary phases. They consist of phenol units linked via methylene bridges and can also form inclusion complexes like the other host supramolecules. The resulting interactions influence the retention factors and improve the selectivity of the solutes. Additionally, modification of the calixarencs, for instance by varying the ring size, substitutents. conformations and pKa values, enable a more enhanced interaction spectrum and can improve the specificity for guest molecules. The application of calixarenes in chromatography also includes medical and environmental applications, preparative chemistry as well as the rapidly developing area of supramolecular chemistry. Taking the possibilities and the growing interests of calixarenes into account, the aim of the review is to summarise the application possibilities and interactions of calixarenes as stationary phase in HPLC.
引用
收藏
页码:161 / 170
页数:10
相关论文
共 123 条
[41]   Preparation and evaluation of an end-capped p-tert-butyl-calix[4]arene-bonded-silica stationary phase for reversed-phase high-performance liquid chromatography [J].
Huai, QY ;
Zhao, B ;
Zuo, YM .
CHROMATOGRAPHIA, 2004, 59 (9-10) :637-645
[42]   Detection of uranyl ion using polymeric membrane containing calix[6]arene uranophile [J].
Hur, Y ;
Lee, Y ;
Jang, G ;
Choi, H ;
Koh, K .
MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 2002, 377 :221-224
[43]   Complexation of the sodium cation by a calix[4]arene tetraester in solution. Formation of a 2:1 calixarene:sodium complex [J].
Israeli, Y ;
Detellier, C .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (10) :1897-1901
[44]   Novel cesium-selective electrodes based on lipophilic 1,3-bisbridged cofacial-calix[6]crowns [J].
Jeon, SW ;
Yeo, HY ;
Lee, HK ;
Ko, SW ;
Nam, KC .
ELECTROANALYSIS, 2004, 16 (06) :472-477
[45]   Membrane transport of neurotransmitter acetylcholine and related compounds across a phospholipid bilayer by a calix[6]arene ester [J].
Jin, T .
CHEMICAL COMMUNICATIONS, 1999, (20) :2129-2130
[46]   Electrochemical recognition of ions with self-assembled monlayers of calixarenes [J].
Kim, H ;
Kim, J ;
Park, J ;
Kim, K ;
Ahn, SJ ;
Chung, TD ;
Chang, SK .
MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 2001, 371 :57-62
[47]  
KNAPMAN K, 2000, CHEM AUST, V67, P16
[48]  
Ko SW, 2002, B KOR CHEM SOC, V23, P1379
[49]  
Krauss GJ, 1998, J PROTEIN CHEM, V17, P515
[50]   Novel urea-linked cinchona-calixarene hybrid-type receptors for efficient chromatographic enantiomer separation of carbamate-protected cyclic amino acids [J].
Krawinkler, KH ;
Maier, NM ;
Sajovic, E ;
Lindner, W .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1053 (1-2) :119-131