Issue 17, 2014

Direction of the polymorphic form of entacapone using an electrochemical tuneable surface template

Abstract

The ability to direct the surface crystallisation of different polymorphs of entacapone by tuning the electrochemical potential of Au(100) templates is demonstrated. Under quiescent conditions, without polarization (at open circuit potential), entacapone crystallises in its stable form A on the template surface and concomitantly in its metastable form D in the bulk solution. When Au(100) is negatively polarized (−150 mV), form D is still formed in the bulk solution but the metastable form α is found to crystallise at the edges of the template. Both crystals of form A and α were observed to grow epitaxially over the Au template surface. The electrochemical templating effect is consistent with the polarisation changing the structure of the initially adsorbed layers of supersaturated solution at the template surface which directs the nuclei formation and the subsequent crystal growth processes. This study demonstrates, for the first time, the direction of polymorphic form using a low field polarized nucleation template.

Graphical abstract: Direction of the polymorphic form of entacapone using an electrochemical tuneable surface template

Article information

Article type
Communication
Submitted
05 Dec 2013
Accepted
10 Mar 2014
First published
10 Mar 2014

CrystEngComm, 2014,16, 3487-3493

Author version available

Direction of the polymorphic form of entacapone using an electrochemical tuneable surface template

A. Kwokal and K. J. Roberts, CrystEngComm, 2014, 16, 3487 DOI: 10.1039/C3CE42473A

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.

Social activity

Spotlight

Advertisements