2012
DOI: 10.1080/00032719.2012.673099
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Dummy Template-Imprinted Polymers for Bisphenol A Prepared Using a Schiff Base-Type Template Molecule with Post-Imprinting Oxidation

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Cited by 21 publications
(8 citation statements)
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“…It is a typical method and often uses readily reversible condensation reactions involving boronate esters, 31 ketals/acetals, 32 and Schiff's base. 33 However, covalent imprinting is regarded as a less flexible method since the reversible condensation reactions are limited. Moreover, it is very difficult to reach thermodynamic equilibrium since the strong covalent interactions will result in slow binding and dissociation.…”
Section: Fundamentals Of Mipsmentioning
confidence: 99%
“…It is a typical method and often uses readily reversible condensation reactions involving boronate esters, 31 ketals/acetals, 32 and Schiff's base. 33 However, covalent imprinting is regarded as a less flexible method since the reversible condensation reactions are limited. Moreover, it is very difficult to reach thermodynamic equilibrium since the strong covalent interactions will result in slow binding and dissociation.…”
Section: Fundamentals Of Mipsmentioning
confidence: 99%
“…An ideal template should satisfy three essential conditions: the template should not have functional groups which restrict its polymerization; it should show high chemical stability during the polymerization process and should contain functional groups which can create complexes with functional monomers. Several types of templates such as ions [ 101 , 102 ], organic molecules (pesticides, pharmaceuticals, amino acids, sugars, endocrine disrupting chemicals, etc.) [ 103 , 104 , 105 ], bio-macromolecules, cells and viruses [ 90 , 106 ] have been reported in MIPs, but the imprinting of proteins and a few bio-macromolecules is still a great challenge for researchers [ 107 ].…”
Section: Molecular Imprintingmentioning
confidence: 99%
“…Another oxidative PIM procedure was designed where a dummy template molecule for BPA, 4,4'-diaminodiphenylmethane was used coupled with two styrenes via Shiff base formation [107] (Fig. 36).…”
Section: Transformation Of Binding Sites Within the Molecularly Imprimentioning
confidence: 99%