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Volumn 11, Issue 1-6, 1998, Pages 69-74

Insights into the origins of binding and the recognition properties of molecularly imprinted polymers prepared using an amide as the hydrogen-bonding functional group

Author keywords

Chiral recognition; Hydrogen bonding; Hydrophobic interactions; Molecular imprinting; Polymer

Indexed keywords

2 VINYLPYRIDINE; ACETONITRILE; ACRYLAMIDE; ENANTIOMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROGEN BOND; HYDROPHOBICITY; METHACRYLIC ACID; MOLECULAR INTERACTION; MOLECULAR SIZE; POLYMER; SOLVENT;

EID: 0032465568     PISSN: 09523499     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-1352(199812)11:1/6<69::AID-JMR392>3.0.CO;2-I     Document Type: Conference Paper
Times cited : (40)

References (21)
  • 1
    • 0029063139 scopus 로고
    • Mimics of the binding sites of opioid receptors obtained by molecular imprinting of enkephalin and morphine
    • Andersson, L. I., Müller, R., Vlatakis, G. and Mosbach, K. (1995). Mimics of the binding sites of opioid receptors obtained by molecular imprinting of enkephalin and morphine. Proc. Natl. Acad. Sci. USA 92, 4788-4792.
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , pp. 4788-4792
    • Andersson, L.I.1    Müller, R.2    Vlatakis, G.3    Mosbach, K.4
  • 2
    • 0028231548 scopus 로고
    • Designed catalysts. a synthetic network polymer that catalyzes the dehydrofluorination of 4-fluoro-4-(p-nitrophenyl)butan-2-one
    • Beach, J. V. and Shea, K. J. (1994). Designed catalysts. A synthetic network polymer that catalyzes the dehydrofluorination of 4-fluoro-4-(p-nitrophenyl)butan-2-one. J. Am. Chem. Soc. 116, 379-380.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 379-380
    • Beach, J.V.1    Shea, K.J.2
  • 3
    • 0026331366 scopus 로고
    • Direct enantioseparation of β-adrenergic blockers using a chiral stationary phase prepared by molecular imprinting
    • Fischer, L., Müller, R., Ekberg, B. and Mosbach, K. (1991). Direct enantioseparation of β-adrenergic blockers using a chiral stationary phase prepared by molecular imprinting. J. Am. Chem. Soc. 113, 9358-9360.
    • (1991) J. Am. Chem. Soc. , vol.113 , pp. 9358-9360
    • Fischer, L.1    Müller, R.2    Ekberg, B.3    Mosbach, K.4
  • 5
    • 0001741309 scopus 로고
    • Introducing biomimetic sensors based on molecularly imprinted polymers as recognition elements
    • Kriz, D., Ramström, O., Svensson, A. and Mosbach, K. (1995). Introducing biomimetic sensors based on molecularly imprinted polymers as recognition elements. Anal. Chem. 67, 2142-2144.
    • (1995) Anal. Chem. , vol.67 , pp. 2142-2144
    • Kriz, D.1    Ramström, O.2    Svensson, A.3    Mosbach, K.4
  • 8
    • 0030049794 scopus 로고    scopus 로고
    • The emerging technique of molecular imprinting and its future impact on biotechnology
    • Mosbach, K. and Ramström, O. (1996). The emerging technique of molecular imprinting and its future impact on biotechnology. Bio/Technology 14, 163-170.
    • (1996) Bio/Technology , vol.14 , pp. 163-170
    • Mosbach, K.1    Ramström, O.2
  • 9
    • 0024692316 scopus 로고
    • Molecular recognition in synthetic polymers. Enantiomeric resolution of amide derivatives of amino acids on molecularly imprinted polymers
    • O'Shannessy, D. J., Andersson, L. I. and Mosbach, K. (1989). Molecular recognition in synthetic polymers. Enantiomeric resolution of amide derivatives of amino acids on molecularly imprinted polymers. J. Mol. Recognit. 2, 1-5.
    • (1989) J. Mol. Recognit. , vol.2 , pp. 1-5
    • O'Shannessy, D.J.1    Andersson, L.I.2    Mosbach, K.3
  • 11
    • 0027717932 scopus 로고
    • Recognition sites incorporating both pyridinyl and carboxy functionalities prepared by molecular imprinting
    • Ramström, O., Andersson, L. I. and Mosbach, K. (1993). Recognition sites incorporating both pyridinyl and carboxy functionalities prepared by molecular imprinting. J. Org. Chem. 58, 7562-7564.
    • (1993) J. Org. Chem. , vol.58 , pp. 7562-7564
    • Ramström, O.1    Andersson, L.I.2    Mosbach, K.3
  • 12
    • 0030224415 scopus 로고    scopus 로고
    • Chiral recognition in adrenergic receptor binding mimics prepared by molecular imprinting
    • Ramström, O., Yu, C. and Mosbach, K. (1996). Chiral recognition in adrenergic receptor binding mimics prepared by molecular imprinting. J. Mol. Recognit. 9, 691-696.
    • (1996) J. Mol. Recognit. , vol.9 , pp. 691-696
    • Ramström, O.1    Yu, C.2    Mosbach, K.3
  • 13
    • 0024055613 scopus 로고
    • Highly enantioselective and substrate-selective polymers obtained by molecular imprinting utilizing noncovalent interactions. NMR and chromatographic studies on the nature of recognition
    • Sellergren, B., Lepistö, M. and Mosbach, K. (1988). Highly enantioselective and substrate-selective polymers obtained by molecular imprinting utilizing noncovalent interactions. NMR and chromatographic studies on the nature of recognition. J. Am. Chem. Soc. 110, 5853-5860.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 5853-5860
    • Sellergren, B.1    Lepistö, M.2    Mosbach, K.3
  • 14
    • 0027424990 scopus 로고
    • Chiral ion-exchange chromatography. Correlation between solute retention and a theoretical ion-exchange model using imprinted polymers
    • Sellergren, B. and Shea, K. J. (1993). Chiral ion-exchange chromatography. Correlation between solute retention and a theoretical ion-exchange model using imprinted polymers. J. Chromatogr. 654, 17-28.
    • (1993) J. Chromatogr. , vol.654 , pp. 17-28
    • Sellergren, B.1    Shea, K.J.2
  • 15
    • 0030922975 scopus 로고    scopus 로고
    • Evaluation of binding and origins of specificity of 9-ethyladenine imprinted polymers
    • Spivak, D., Gilmore, M. A. and Shea, K. J. (1997). Evaluation of binding and origins of specificity of 9-ethyladenine imprinted polymers. J. Am. Chem. Soc. 119, 4388-4393.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 4388-4393
    • Spivak, D.1    Gilmore, M.A.2    Shea, K.J.3
  • 16
    • 33845374118 scopus 로고
    • Hydrogen bonding between solutes in aqueous solution
    • Stahl, N. and Jencks, W. P. (1986). Hydrogen bonding between solutes in aqueous solution. J. Am. Chem. Soc. 108, 4196-4205.
    • (1986) J. Am. Chem. Soc. , vol.108 , pp. 4196-4205
    • Stahl, N.1    Jencks, W.P.2
  • 17
    • 0027447855 scopus 로고
    • Drug assay using antibody mimics made by molecular imprinting
    • Vlatakis, G., Andersson, L. I., Müller, R. and Mosbach, K. (1993). Drug assay using antibody mimics made by molecular imprinting. Nature 361, 645-647.
    • (1993) Nature , vol.361 , pp. 645-647
    • Vlatakis, G.1    Andersson, L.I.2    Müller, R.3    Mosbach, K.4
  • 18
    • 0000848029 scopus 로고
    • A new method for the introduction of recognition site functionality into polymers prepared by molecular imprinting: Synthesis and characterization of polymeric receptors for cholesterol
    • Whitcombe, M. J., Rodriguez, M. E., Villar, P. and Vulfson, E. N. (1995). A new method for the introduction of recognition site functionality into polymers prepared by molecular imprinting: synthesis and characterization of polymeric receptors for cholesterol. J. Am. Chem. Soc. 117, 7105-7111.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 7105-7111
    • Whitcombe, M.J.1    Rodriguez, M.E.2    Villar, P.3    Vulfson, E.N.4
  • 19
    • 0028873867 scopus 로고
    • Molecular imprinting in cross-linked materials with the aid of molecular templates - A way towards artificial antibodies
    • Wulff, G. (1995). Molecular imprinting in cross-linked materials with the aid of molecular templates - a way towards artificial antibodies. Angew. Chem. Int. Ed. Engl. 34, 1812-1832.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 1812-1832
    • Wulff, G.1
  • 20
    • 0001107490 scopus 로고    scopus 로고
    • Molecular imprinting utilizing an amide functional group for hydrogen bonding leading to highly efficient polymers
    • Yu, C. and Mosbach, K. (1997). Molecular imprinting utilizing an amide functional group for hydrogen bonding leading to highly efficient polymers. J. Org. Chem. 62, 4057-4064.
    • (1997) J. Org. Chem. , vol.62 , pp. 4057-4064
    • Yu, C.1    Mosbach, K.2
  • 21
    • 0030732388 scopus 로고    scopus 로고
    • Enantiomeric recognition by molecularly imprinted polymers using hydrophobic interactions
    • Yu, C., Ramström, O. and Mosbach, K. (1997). Enantiomeric recognition by molecularly imprinted polymers using hydrophobic interactions. Anal. Lett. 30, 2123-2140.
    • (1997) Anal. Lett. , vol.30 , pp. 2123-2140
    • Yu, C.1    Ramström, O.2    Mosbach, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.