Issue 4, 2015

Studies on polymorph conversion in a new cyclodextrin inclusion compound

Abstract

A novel β-cyclodextrin (βCD) inclusion compound was prepared using 4-phenylpyridine-N-oxide (PPNO) as the organic guest. The inclusion compound, βCD·PPNO, was characterised both in solution and in the solid state using numerous techniques. 1H NMR in aqueous solution allowed the determination of a 1 : 1 stoichiometry and an association constant of 164 ± 21 M−1. Powder and single-crystal X-ray diffraction studies showed the formation of two distinct crystal phases, appearing at different timings. Over time, one of the crystal phases converts spontaneously into the other. This work is the first to monitor the conversion of different polymorphs of cyclodextrin inclusion compounds in real time.

Graphical abstract: Studies on polymorph conversion in a new cyclodextrin inclusion compound

Supplementary files

Article information

Article type
Paper
Submitted
09 Oct 2014
Accepted
21 Nov 2014
First published
25 Nov 2014

CrystEngComm, 2015,17, 937-946

Studies on polymorph conversion in a new cyclodextrin inclusion compound

J. A. Fernandes, A. I. Ramos, P. Ribeiro-Claro, F. A. Almeida Paz and S. S. Braga, CrystEngComm, 2015, 17, 937 DOI: 10.1039/C4CE02041C

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