Issue 14, 1989

Molecular imprinting of a transition state analogue leads to a polymer exhibiting esterolytic activity

Abstract

Molecular imprinting of p-nitrophenyl methylphosphonate, a transition state analogue, in poly[4(5)-vinylimidazole] leads to a polymer which hydrolyses p-nitrophenyl acetate at an increased rate and which can then be inhibited by addition of the p-nitrophenol methylphosphonate.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 969-970

Molecular imprinting of a transition state analogue leads to a polymer exhibiting esterolytic activity

D. K. Robinson and K. Mosbach, J. Chem. Soc., Chem. Commun., 1989, 969 DOI: 10.1039/C39890000969

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements