dc.contributor.author |
Eccles, Kevin S. |
|
dc.contributor.author |
Elcoate, Curtis J. |
|
dc.contributor.author |
Stokes, Stephen P. |
|
dc.contributor.author |
Maguire, Anita R. |
|
dc.contributor.author |
Lawrence, Simon E. |
|
dc.date.accessioned |
2014-03-03T10:25:46Z |
|
dc.date.available |
2014-03-03T10:25:46Z |
|
dc.date.issued |
2010-10 |
|
dc.identifier.citation |
ECCLES, K. S., ELCOATE, C. J., STOKES, S. P., MAGUIRE, A. R. & LAWRENCE, S. E. 2010. Sulfoxides: Potent Co-Crystal Formers. Crystal Growth & Design, 10, 4243-4245. |
en |
dc.identifier.volume |
10 |
en |
dc.identifier.issued |
10 |
en |
dc.identifier.startpage |
4243 |
en |
dc.identifier.endpage |
4245 |
en |
dc.identifier.issn |
1528-7483 |
|
dc.identifier.uri |
http://hdl.handle.net/10468/1420 |
|
dc.identifier.doi |
10.1021/cg1010192 |
|
dc.description.abstract |
The design of co-crystals requires knowledge of robust supramol. synthons. The sulfoxide is a potent H bond acceptor and was used as a co-crystal former with a range of NH functional groups, via N-H···O=S H bonds. The NH functional group retains favorable H bond motifs from its own structure in all cases where this is possible, with the sulfoxide interacting in a discrete, capping fashion in four cases and in a bifurcated, bridging fashion in the three other cases presented here. Crystallog. data are given for 7 co-formers, dibenzyl sulfoxide and cyclohexanecarbothioamide. |
en |
dc.description.sponsorship |
Science Foundation Ireland under (SRC/B1158 (CE)); Science Foundation Ireland (05/PICA/B802/EC07) |
en |
dc.format.mimetype |
application/pdf |
en |
dc.language.iso |
en |
en |
dc.publisher |
American Chemical Society |
en |
dc.relation.uri |
http://pubs.acs.org/doi/abs/10.1021/cg1010192 |
|
dc.rights |
© 2010, American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in Crystal Growth & Design, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see http://pubs.acs.org/doi/abs/10.1021/cg1010192 |
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dc.subject |
Crystallography and liquid crystals |
en |
dc.title |
Sulfoxides: potent co-crystal formers |
en |
dc.type |
Article (peer-reviewed) |
en |
dc.internal.authorcontactother |
Simon Lawrence, Chemistry, University College Cork, Cork, Ireland. +353-21-490-3000 Email: simon.lawrence@ucc.ie |
en |
dc.internal.availability |
Full text available |
en |
dc.date.updated |
2013-01-08T11:44:34Z |
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dc.description.version |
Accepted Version |
en |
dc.internal.rssid |
57685675 |
|
dc.contributor.funder |
Science Foundation Ireland |
en |
dc.description.status |
Peer reviewed |
en |
dc.identifier.journaltitle |
Crystal Growth & Design |
en |
dc.internal.copyrightchecked |
No Breeda, from your spreadsheet: "Accepted Version - Include set statement - 12 month embargo If mandated by funding agency, employer. Must receive written permission" !!CORA!! AV and set statement. |
en |
dc.internal.licenseacceptance |
Yes |
en |
dc.internal.IRISemailaddress |
simon.lawrence@ucc.ie |
en |