Influence of polymerization temperature on the molecular recognition of imprinted polymers

被引:50
|
作者
Lu, Y [1 ]
Li, CX [1 ]
Wang, XD [1 ]
Sun, PC [1 ]
Xing, XH [1 ]
机构
[1] Nankai Univ, Inst Polymer Chem, State Key Lab Funct Polymer Mat Adsorpt & Separat, Tianjin 300071, Peoples R China
关键词
polymerization temperature; molecular recognition; molecular imprinting polymers;
D O I
10.1016/j.jchromb.2003.10.013
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
This paper aimed at investigating the influence of polymerization temperature on the molecular recognition of molecularly imprinted polymers (MIPs) based on multiple non-covalent interactions. 3-L-Phenylaianylaminopyridine (3-L-PheNHPy) imprinted polymers were prepared using azobisnitriles as either thermal initiators or photoinitiators at various temperatures of 10, 40 and 60degreesC, respectively. These polymers were subsequently evaluated in the high-performance liquid chromatographic (HPLC) mode for enantioselectivity. An unexpected result shows that polymer prepared at 40degreesC has the highest enantioselectivity, but not the polymer prepared at lower temperature of 10degreesC. Further, the effect of elution temperature and sample load on the selectivity of polymers was investigated in detail. In order to get a better understanding of the "exception", the influence of polymerization temperature on the polymerization extent and polymer morphology was studied by FT-IR spectrum test, cross-polarization magic angle spinning (CP-MAS) C-13 NMR spectra experiment and pore analysis. Based on these results we attribute this "exception" to that there is a tradeoff between the extent of polymerization and stabilization of the template-functional monomer complexes. And an optimal polymerization temperature can be found for each combination of template and monomer. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 59
页数:7
相关论文
共 50 条
  • [21] Recent applications of molecular imprinted polymers for enantio-selective recognition
    Cheong, Won Jo
    Ali, Faiz
    Choi, Ji Ho
    Lee, Jin Ook
    Sung, Kim Yune
    TALANTA, 2013, 106 : 45 - 59
  • [22] Imprinted polymers: artificial molecular recognition materials with applications in synthesis and catalysis
    Alexander, C
    Davidson, L
    Hayes, W
    TETRAHEDRON, 2003, 59 (12) : 2025 - 2057
  • [23] Molecular recognition properties and adsorption isotherms of diniconaziole-imprinted polymers
    Liu, HY
    Yang, GL
    Liu, SB
    Wang, MM
    Chen, Y
    JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES, 2005, 28 (15) : 2315 - 2323
  • [24] Separation and sensing based on molecular recognition using molecularly imprinted polymers
    Takeuchi, T
    Haginaka, J
    JOURNAL OF CHROMATOGRAPHY B, 1999, 728 (01): : 1 - 20
  • [25] Syntheses of molecularly imprinted polymers and their molecular recognition study for doxazosin mesylate
    Wang, HY
    Jiang, JG
    Ma, LY
    Pang, YL
    REACTIVE & FUNCTIONAL POLYMERS, 2005, 64 (02): : 119 - 126
  • [26] Solvent dependent specific driving forces in the molecular recognition in imprinted polymers
    Sellergren, B
    Dauwe, C
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1997, 213 : 27 - IEC
  • [27] Clozapine Recognition via Molecularly Imprinted Polymers; Bulk Polymerization Versus Precipitation Method
    Mohajeri, Seyed Ahmad
    Karimi, Gholamreza
    Aghamohammadian, Javad
    Khansari, Mehdi Rajabnia
    JOURNAL OF APPLIED POLYMER SCIENCE, 2011, 121 (06) : 3590 - 3595
  • [28] Living Radical Polymerization and Molecular Imprinting: Improving Polymer Morphology in Imprinted Polymers
    Salian, Vishal D.
    Byrne, Mark E.
    MACROMOLECULAR MATERIALS AND ENGINEERING, 2013, 298 (04) : 379 - 390
  • [29] Analysis of recognition of fructose by imprinted polymers
    Rajkumar, Rajagopal
    Warsinke, Axel
    Moehwald, Helmuth
    Scheller, Frieder W.
    Katterle, Martin
    TALANTA, 2008, 76 (05) : 1119 - 1123
  • [30] Molecularly imprinted polymers for dopamine recognition
    Cheek, Tesla
    Mwangi, George
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2017, 253