Abstract
The catalytic activities of l-histidyl group-introduced, cross-linked polymers imprinted by a transition-state analogue (phenyl 1-benzyloxycarbonylamino-3-methylpentylphosphonate) or a ground-state one ( N-( N-benzyloxycarbonyl- l-leucinoyl) anthranilic acid) for the esterolysis of a marked substrate of p-nitrophenyl N-benzyloxycarbonyl- l-leucinate were examined in the hydrolysis of amino acid esters; a transition-state analogue recorded polymer possessing a low cross-linker content (8.7%) exhibited the highest catalytic activity for the marked substrate hydrolysis with the positively largest activation entropy and the smallest activation free energy.
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