Co-crystals of an agrochemical active A pyridine-amine synthon for a thioamide group

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Show simple item record Nauha, Elisa Nissinen, Maija 2012-01-13T11:34:02Z 2012-01-13T11:34:02Z 2011
dc.identifier.citation Nauha, E., & Nissinen, M. (2011). Co-crystals of an agrochemical active – A pyridine-amine synthon for a thioamide group. <em>Journal of Molecular Structure</em>, 1006 (1-3), 566-569. <a href="">doi:10.1016/j.molstruc.2011.10.004</a> fi
dc.identifier.issn 0022-2860
dc.identifier.other TUTKAID_47528
dc.description.abstract Five novel co-crystals of thiophanate-ethyl (TE), an agrochemical active, with di(2-pyridyl)ketone (1), 2-benzoylpyridine (2), 3-benzoylpyridine (3), 4-phenylpyridine (4) and biphenyl (5) were found and crystal structures of four of them (TE1–TE3, TE5) solved by single crystal X-ray diffraction. Three of the co-crystals (TE1–TE3) form by way of a reliable pyridine-amine hydrogen bond synthon and one (TE5) because of close packing effects. The fifth co-crystal was identified by X-ray powder diffraction. The work demonstrates the usage of a reliable supramolecular synthon for crystal engineering, while concurrently reminds that the close packing of even very similar molecules cannot be fully predicted. fi
dc.language.iso eng
dc.publisher Elsevier
dc.relation.ispartofseries Journal of Molecular Structure
dc.rights © 2011 Elsevier B.V. All rights reserved. This is an electronic final draft version of an article whose final and definitive form has been published in Journal of Molecular Structure by Elsevier.
dc.rights openAccess fi
dc.subject.other cocrystal en
dc.subject.other co-crystal en
dc.subject.other supramolecular synthon en
dc.subject.other X-ray diffraction en
dc.subject.other yhteiskide fi
dc.subject.other supramolekyyli fi
dc.subject.other röntgen diffraktio fi
dc.title Co-crystals of an agrochemical active A pyridine-amine synthon for a thioamide group
dc.type Article
dc.identifier.urn URN:NBN:fi:jyu-201201121021
dc.subject.kota 116
dc.contributor.laitos Kemian laitos fi
dc.contributor.laitos Department of Chemistry en
dc.contributor.oppiaine orgaaninen kemia fi
dc.identifier.volume 1006
dc.identifier.issue 1-3
jyx.tutka.pagetopage 566-569
dc.identifier.doi 10.1016/j.molstruc.2011.10.004 2012-01-12T04:30:14Z
dc.description.version Final Draft
dc.type.coar journal article
dc.description.reviewstatus peerReviewed
dc.format.pagerange 566-569
dc.relation.issn 0022-2860
dc.type.version acceptedVersion

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