Sulfoxides: potent co-crystal formers

Eccles, Kevin S.; Elcoate, Curtis J.; Stokes, Stephen P.; Maguire, Anita R.; Lawrence, Simon E.

doi:10.1021/cg1010192

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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	en
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
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