메뉴 건너뛰기




Volumn 46, Issue 5, 2011, Pages 809-817

Loading effects and adsorption isotherms for single and dual chiral systems applying ligand exchange chromatography

Author keywords

Adsorption isotherms; Chiral dual system; Ligand exchange chromatography; Loading effects

Indexed keywords

ADSORPTION BEHAVIOR; BASE LINE; CAPACITY FACTORS; CHIRAL COLUMN; CHIRAL DUAL SYSTEM; CHIRAL SELECTOR; CHIRAL SYSTEMS; DUAL SYSTEM; LIGAND EXCHANGE CHROMATOGRAPHY; LINEAR RANGE; LOADING EFFECTS; MOBILE PHASE; RACEMIC MIXTURES;

EID: 79953194125     PISSN: 01496395     EISSN: 15205754     Source Type: Journal    
DOI: 10.1080/01496395.2010.539192     Document Type: Article
Times cited : (2)

References (33)
  • 2
    • 0345490722 scopus 로고    scopus 로고
    • Elelctrochromatographic enantioseparation using chiral ligand exchange monolithic sol-gel column
    • Chen, Z.; Nishiyama, T.; Uchiyama, K.; Hobo, T. (2004) Elelctrochromatographic enantioseparation using chiral ligand exchange monolithic sol-gel column. Anal. Chim. Acta, 501 (1): 17.
    • (2004) Anal. Chim. Acta , vol.501 , Issue.1 , pp. 17
    • Chen, Z.1    Nishiyama, T.2    Uchiyama, K.3    Hobo, T.4
  • 3
    • 74849137289 scopus 로고    scopus 로고
    • Enantioseparation of alpha-amino acids on an 18-crown-6-tetracarboxylic acid-bonded silica by capillary elelctrochromatography
    • Lee, T.; Lee, W.; Hyun, M.H.; Park, J.H. (2010) Enantioseparation of alpha-amino acids on an 18-crown-6-tetracarboxylic acid-bonded silica by capillary elelctrochromatography. J. Chromatogr. A, 1217 (8): 1425.
    • (2010) J. Chromatogr. A , vol.1217 , Issue.8 , pp. 1425
    • Lee, T.1    Lee, W.2    Hyun, M.H.3    Park, J.H.4
  • 7
    • 60549102528 scopus 로고    scopus 로고
    • Enantiomer self-disproportionation of chiral compounds on achiral ordered mesoporous silica M41S and regular silica gel as a stationary phase
    • Mayani, V.J.; Abdi, H.R.; Kureshy, R.I.; Khan, N.H.; Agrawal, S.; Jasra, R.V. (2009) Enantiomer self-disproportionation of chiral compounds on achiral ordered mesoporous silica M41S and regular silica gel as a stationary phase. Chirality, 21: 255.
    • (2009) Chirality , vol.21 , pp. 255
    • Mayani, V.J.1    Abdi, H.R.2    Kureshy, R.I.3    Khan, N.H.4    Agrawal, S.5    Jasra, R.V.6
  • 9
    • 74449090371 scopus 로고    scopus 로고
    • Selfdisproportionation of enantiomers of 3,3,3-trifluorolactic acid amides via sublimation
    • Yasumoto, M.; Ueki, H.; Soloshonok, V.A. (2010) Selfdisproportionation of enantiomers of 3,3,3-trifluorolactic acid amides via sublimation. J. Fluor. Chem., 131: 266.
    • (2010) J. Fluor. Chem. , vol.131 , pp. 266
    • Yasumoto, M.1    Ueki, H.2    Soloshonok, V.A.3
  • 10
    • 77949485705 scopus 로고    scopus 로고
    • Selfdisproportionation of enantiomers of α-trifluoromethyl lactic acid amides via sublimation
    • Yasumoto, M.; Ueki, H.; Soloshonok, V.A. (2010) Selfdisproportionation of enantiomers of α-trifluoromethyl lactic acid amides via sublimation. J. Fluor. Chem., 131: 540.
    • (2010) J. Fluor. Chem. , vol.131 , pp. 540
    • Yasumoto, M.1    Ueki, H.2    Soloshonok, V.A.3
  • 11
    • 77949492088 scopus 로고    scopus 로고
    • Self-disproportionation of isopropyl 3,3,3-(trifluoro) lactate via sublimation: Sublimation rates vs. enantiomeric composition
    • Yasumoto, M.; Ueki, H.; Ono, T.; Katagiri, T.; Soloshonok, V.A. (2010) Self-disproportionation of isopropyl 3,3,3-(trifluoro) lactate via sublimation: Sublimation rates vs. enantiomeric composition. J. Fluor. Chem., 131: 535.
    • (2010) J. Fluor. Chem. , vol.131 , pp. 535
    • Yasumoto, M.1    Ueki, H.2    Ono, T.3    Katagiri, T.4    Soloshonok, V.A.5
  • 12
    • 0032934315 scopus 로고    scopus 로고
    • Joint use of cyclodextrine additives in chiral discrimination by reversed-phase high-performance liquid chromatography: Temperature effects
    • Bielejewska, A.; Nowakowski, R.; Duszczyk, K.; Sybilska, D. (1999) Joint use of cyclodextrine additives in chiral discrimination by reversed-phase high-performance liquid chromatography: Temperature effects. J of Chromatogr. A, 840 (2): 159.
    • (1999) J of Chromatogr. A , vol.840 , Issue.2 , pp. 159
    • Bielejewska, A.1    Nowakowski, R.2    Duszczyk, K.3    Sybilska, D.4
  • 13
    • 0037967830 scopus 로고    scopus 로고
    • Determination of the single component and competitive adsorption isotherms of the 1-indanol enantiomers by the inverse method
    • Felinger, A.; Zhou, D.; Guiochon, G. (2003) Determination of the single component and competitive adsorption isotherms of the 1-indanol enantiomers by the inverse method. J. Chromatogr. A, 1005 (1-2): 35.
    • (2003) J. Chromatogr. A , vol.1005 , Issue.1-2 , pp. 35
    • Felinger, A.1    Zhou, D.2    Guiochon, G.3
  • 14
    • 0003151814 scopus 로고    scopus 로고
    • Combinatorial approaches to recognition of chirality: Preparation and use of materiels for separartion of enantiomers
    • In, Subramanian, G., ed.; Wiley VCH: Weinheim
    • Svec, F.; Wulff, D.; Frechat, J.M. (2001) Combinatorial approaches to recognition of chirality: Preparation and use of materiels for separartion of enantiomers. In: Chiral Separation Techniques, Subramanian, G., ed.; Wiley VCH: Weinheim, pp. 58-96.
    • (2001) Chiral Separation Techniques , pp. 58-96
    • Svec, F.1    Wulff, D.2    Frechat, J.M.3
  • 16
    • 2942739123 scopus 로고    scopus 로고
    • Chiral separation by HPLC using the ligand-exchange principle
    • Davankov, V.A. (2004) Chiral separation by HPLC using the ligand-exchange principle. Methods Mol. Biol., 243: 207.
    • (2004) Methods Mol. Biol. , vol.243 , pp. 207
    • Davankov, V.A.1
  • 17
    • 62649159011 scopus 로고    scopus 로고
    • The effect of copper(II) salt anion in the chiral ligand-exchange chromatography of amino acids
    • Natalini, B.; Sardella R.; Carbone, G.; Macchiarulo, A.; Pellicciari, R. (2009) The effect of copper(II) salt anion in the chiral ligand-exchange chromatography of amino acids. Anal. Chim. Acta, 638 (2): 225.
    • (2009) Anal. Chim. Acta , vol.638 , Issue.2 , pp. 225
    • Natalini, B.1    Sardella, R.2    Carbone, G.3    Macchiarulo, A.4    Pellicciari, R.5
  • 18
    • 67349208398 scopus 로고    scopus 로고
    • Preparative separation of ketoprofen enantiomers: Choice of mobile phase composition and measurement of competitive adosprtion isotherms
    • Ribeiro, A.E.; Graca, N.S.; Pais, L.S.; Rodrigues, A.E. (2009) Preparative separation of ketoprofen enantiomers: Choice of mobile phase composition and measurement of competitive adosprtion isotherms. Sep. and Pur. Technol., 68: 9.
    • (2009) Sep. and Pur. Technol. , vol.68 , pp. 9
    • Ribeiro, A.E.1    Graca, N.S.2    Pais, L.S.3    Rodrigues, A.E.4
  • 19
    • 0024523595 scopus 로고
    • Racemates versus enantiomerically pure drugs: Putting high-performance liquid chromatography to work in the selection process
    • Krstulovic, A.M. (1989) Racemates versus enantiomerically pure drugs: putting high-performance liquid chromatography to work in the selection process. J. Chromatogr., 488: 53.
    • (1989) J. Chromatogr. , vol.488 , pp. 53
    • Krstulovic, A.M.1
  • 20
    • 77951622817 scopus 로고    scopus 로고
    • Non-ionic surfactant modified ligand exchange chromatography using copper (II) complex of N, Ndimethyl-l-phenylalanine as the chiral additive for enantioselective amino acids separation
    • Dimitrova, P.; Bart, H.-J. (2010) Non-ionic surfactant modified ligand exchange chromatography using copper (II) complex of N, Ndimethyl-l-phenylalanine as the chiral additive for enantioselective amino acids separation. Anal. Chimica Acta, 663 (1): 109.
    • (2010) Anal. Chimica Acta , vol.663 , Issue.1 , pp. 109
    • Dimitrova, P.1    Bart, H.-J.2
  • 21
    • 0007310356 scopus 로고
    • Ligand-exchange chromatography of chiral compounds
    • In, Cagniant, D., ed.; Marcel Dekker: New York
    • Davankov, V.A. (1992) Ligand-exchange chromatography of chiral compounds. In: Complexation Chromatography, Cagniant, D., ed.; Marcel Dekker: New York.
    • (1992) Complexation Chromatography
    • Davankov, V.A.1
  • 22
    • 0023673948 scopus 로고
    • Improved resolution of enantiomers of naproxen by the simultaneous use of chiral stationary phase and a chiral additive in the mobile phase
    • Pettersson, C.; Gioelo, C. (1988) Improved resolution of enantiomers of naproxen by the simultaneous use of chiral stationary phase and a chiral additive in the mobile phase. J. Chromatogr., 435 (1): 225.
    • (1988) J. Chromatogr. , vol.435 , Issue.1 , pp. 225
    • Pettersson, C.1    Gioelo, C.2
  • 23
    • 0037159497 scopus 로고    scopus 로고
    • Comparative study on the enantiomer separation of 1,1′-binaphthyl-2,2′diyl hydrogenphosphate and 1,1′-bi-2-naphthol by liquid chromatography and capillary electrophoresis using single and combined chiral selelctor systems
    • Bielejewska, A.; Duszczyk, K.; Kwaterczak, A.; Sybilska, D. (2002) Comparative study on the enantiomer separation of 1,1′-binaphthyl-2,2′diyl hydrogenphosphate and 1,1′-bi-2-naphthol by liquid chromatography and capillary electrophoresis using single and combined chiral selelctor systems. J of Chromatogr. A, 977 (2): 225.
    • (2002) J of Chromatogr. A , vol.977 , Issue.2 , pp. 225
    • Bielejewska, A.1    Duszczyk, K.2    Kwaterczak, A.3    Sybilska, D.4
  • 24
    • 1842531375 scopus 로고    scopus 로고
    • Chiral discrimination of multiple profens as diastereomeric (R)-(+)-1-phenylethylamides by achiral dual-column gas chromatography
    • Paik, M.-J.; Lee, Y.; Goto, J.; Kim, K.-R. (2004) Chiral discrimination of multiple profens as diastereomeric (R)-(+)-1-phenylethylamides by achiral dual-column gas chromatography. J. Chromatogr. B, 803 (2): 257.
    • (2004) J. Chromatogr. B , vol.803 , Issue.2 , pp. 257
    • Paik, M.-J.1    Lee, Y.2    Goto, J.3    Kim, K.-R.4
  • 25
    • 0036802574 scopus 로고    scopus 로고
    • Selectivity tuning in chiral dual column gas chromatography D. W
    • Krupcik, J.; Spanik, I.; Benicka, E.; Zabka, M.; Aermstrong (2002) Selectivity tuning in chiral dual column gas chromatography D.W. J. Chrom. Sci., 40 (9): 483.
    • (2002) J. Chrom. Sci. , vol.40 , Issue.9 , pp. 483
    • Krupcik, J.1    Spanik, I.2    Benicka, E.3    Zabka, M.4    Aermstrong5
  • 26
    • 0031807742 scopus 로고    scopus 로고
    • Dual chiral recognition system involving cyclodextrine derivatives in capillary electrophoresis II. Enhancement of enantioselectivity
    • Jakubetz, H.; Juza, M.; Schurig, V. (1998) Dual chiral recognition system involving cyclodextrine derivatives in capillary electrophoresis II. Enhancement of enantioselectivity. Electrophoresis, 19 (5): 738.
    • (1998) Electrophoresis , vol.19 , Issue.5 , pp. 738
    • Jakubetz, H.1    Juza, M.2    Schurig, V.3
  • 27
    • 0001733232 scopus 로고    scopus 로고
    • Adsorption isotherms: Experimental determination and application to preparative chromatography
    • Nicoud, R.M.; Seidel-Morgenstern, A. (1996) Adsorption isotherms: Experimental determination and application to preparative chromatography. Isol. Purif., 2: 165.
    • (1996) Isol. Purif. , vol.2 , pp. 165
    • Nicoud, R.M.1    Seidel-Morgenstern, A.2
  • 28
    • 77950260600 scopus 로고    scopus 로고
    • Separation of racemic mixtures of amino acids using chiral eluents
    • Dimitrova, P.; Bart, H.-J. (2010) Separation of racemic mixtures of amino acids using chiral eluents. Chem. Biochem. Eng. Q, 24 (1): 75.
    • (2010) Chem. Biochem. Eng. Q , vol.24 , Issue.1 , pp. 75
    • Dimitrova, P.1    Bart, H.-J.2
  • 29
    • 0028278776 scopus 로고
    • Unusual peak disortion in ligand-exchange chromatography of enantiomers under overloaded conditions
    • Kurganov, A.; Davankov, A.; Unger, K.; Eisenbeiss, F.; Kinkel, J. (1994) Unusual peak disortion in ligand-exchange chromatography of enantiomers under overloaded conditions. J. Chromatogr., 666 (1-2): 99.
    • (1994) J. Chromatogr. , vol.666 , Issue.1-2 , pp. 99
    • Kurganov, A.1    Davankov, A.2    Unger, K.3    Eisenbeiss, F.4    Kinkel, J.5
  • 30
    • 0000417993 scopus 로고
    • Resolution of α-amino acids on reversed-phase silica gels coated with N-decyl-Lhystidine
    • Davankov, V.A.; Bochkov, A.S.; Belov, Yu.P. (1981) Resolution of α-amino acids on reversed-phase silica gels coated with N-decyl-Lhystidine. J. Chromatogr., 218: 547.
    • (1981) J. Chromatogr. , vol.218 , pp. 547
    • Davankov, V.A.1    Bochkov, A.S.2    Belov, Y.P.3
  • 31
    • 34547784410 scopus 로고    scopus 로고
    • Tunable peak deformations in chiral liquid chromatography
    • Anell, R.; Forssén, P.; Formstedt, T. (2007) Tunable peak deformations in chiral liquid chromatography. Anal. Chem., 79 (15): 5838.
    • (2007) Anal. Chem. , vol.79 , Issue.15 , pp. 5838
    • Anell, R.1    Forssén, P.2    Formstedt, T.3
  • 32
    • 33947171097 scopus 로고    scopus 로고
    • Preparative chromatographic separation of amino acid racemic mixtures I. Adsorption isotherms
    • Kostova, A.; Bart, H.-J. (2007) Preparative chromatographic separation of amino acid racemic mixtures I. Adsorption isotherms. Sep. and Pur. Technol., 54: 340.
    • (2007) Sep. and Pur. Technol. , vol.54 , pp. 340
    • Kostova, A.1    Bart, H.-J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.