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Abstrakty
An amphiphilic calix[4]arene with sulfonate groups on the lower rim has been investigated as a buffer additive for separation of positional isomers by capillary electrophoresis. Addition of the compound to the run-ning buffer led to successful separation of positional isomers of nitrophenols, dinitrobenzenes, and benzenediols. Association constants between the calixarene and the analytes indicated that size-selective host–guest inter-actions between them played a prominent role in determining the separation behavior.
Słowa kluczowe
Czasopismo
Rocznik
Tom
Strony
73--80
Opis fizyczny
Bibliogr. 20 poz., rys., tab.
Twórcy
autor
autor
autor
autor
- Department of Chemistry, Faculty of Engineering, Gunma University, 1-5-1 Tenjin-cho, Kiryu, 376-8515, Japan
Bibliografia
- [1] P.D. Grossman and J.C. Colburn, Capillary Electrophoresis, Theory and Practice, Academic Press, San Diego, 1992
- [2] K. Takahashi, T. Nakagawa, and T. Imato, Anal. Commun., 35, 221 (1998)
- [3] C. Chiou and J. Shih, Analyst (London), 121, 1107 (1996)
- [4] Y. He and H. K. Lee, J. Chromatogr. A, 749, 227 (1996)
- [5] R. Tait, D. Thompson, V. Stella, and J. Stobaugh, Anal. Chem., 66, 4013 (1994)
- [6] M.S. Pena, Y. Zhang, and I.M. Warner, Anal. Chem., 69, 3239 (1997)
- [7] S. Sun, M.J. Sepaniak, J.S. Wang, and C.D. Gutsche, Anal. Chem., 69, 344 (1997)
- [8] T. Zhao, X. Hu, J. Cheng, and X. Lu, Anal. Chim. Acta, 358, 263 (1998)
- [9] W.C. Yang, X.D. Yu, A.M. Yu, and H.Y. Chen, J. Chromatogr. A, 910, 311 (2001)
- [10] M. Mori, H. Naraoka, H. Tsue, T. Morozumi, T. Kaneta, and S. Tanaka, Anal. Sci., 17, 763 (2001)
- [11] C.D. Gutsche, Calixarenes. In: J.F. Stoddart (Ed.) Monographs in Supramolecular Chemistry, Royal Society of Chemistry, Cambridge, 1989
- [12] C.D. Gutsche, Calixarenes Revisited. In: J.F. Stoddart (Ed.) Monographs in Supramolecular Chemistry, Royal Society of Chemistry, Cambridge, 1998
- [13] Z. Asfari, V. Böhmer, J. Harrowfield, J. Vicens, and M. Saadioui (Eds) Calixarenes 2001, Kluwer, Dordrecht, 2001
- [14] H. Tsue, T. Takimoto, C. Kikuchi, H. Yanase, H. Takahashi, K. Amezawa, K Ishibashi, S. Tanaka, and R. Tamura, Chem. Lett., 34, 1030 (2005)
- [15] S. Shinkai, T. Arimura, K. Araki, H. Kawabata, H. Satoh, T. Tsubaki, O. Manabe, and J. Sunamoto, J. Chem. Soc. Perkin Trans. 1, 2039 (1989)
- [16] P.K. Glasoe, J. Phys. Chem., 69, 4416 (1965)
- [17] R. Kuhn, R. Frei, and M. Christen, Anal. Biochem., 218, 131 (1994)
- [18] H. Benesi and J. Hildebrand, J. Am. Chem. Soc., 71, 2703 (1949)
- [19] R.T. Morrison and R.N. Boyd, Organic Chemistry, 3rd edn, Allyn and Bacon, Boston, 1975
- [20] S. Budavari, The Merck Index, 12th edn, Merck Research Laboratories, Merck, Whitehouse Station, NJ, USA, 1996
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BATA-0003-0006