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dc.contributor.authorNauha, Elisa
dc.contributor.authorKolehmainen, Erkki
dc.contributor.authorNissinen, Maija
dc.date.accessioned2011-11-16T05:35:21Z
dc.date.available2012-09-01T21:45:03Z
dc.date.issued2011
dc.identifier.citationNauha, E., Kolehmainen, E., & Nissinen, M. (2011). Packing incentives and a reliable N–H...N–pyridine synthon in co-crystallization of bipyridines with two agrochemical actives. <em>CrystEngComm</em>, 13 (21), 6531-6537. <a href="http://dx.doi.org/10.1039/C1CE05730H">doi:10.1039/C1CE05730H</a>fi
dc.identifier.otherTUTKAID_47525
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/36953
dc.description.abstractThe co-crystallization of agrochemical actives thiophanate-methyl and thiophanate-ethyl with 2,2′-bipyridine, 4,4′-bipyridine and 1,2-bis(4-pyridyl)ethane was investigated with conventional crystallization, the slurry method and liquid-assisted grinding. Co-crystals of both thiophanates with all bipyridines were found and the structures solved with single crystal X-ray diffraction. Whereas the 2,2′-bipyridine co-crystals seem to form because of a combination of weak interactions, and in the case of the thiophanate-methyl, partly because of close packing incentives, the 4,4′-bipyridine and 1,2-bis(4-pyridyl)ethane co-crystals form mainly because of a favourable N–H···N–pyridine hydrogen bonding synthon.
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.relation.ispartofseriesCrystEngComm
dc.subject.othercocrystalen
dc.subject.otherco-crystalen
dc.subject.othersupramolecular synthonen
dc.subject.otherX-ray diffractionen
dc.subject.otheryhteiskidefi
dc.subject.othersupramolekyylifi
dc.subject.otherröntgen diffraktiofi
dc.titlePacking incentives and a reliable N–H···N pyridine synthon in co-crystallization of bipyridines with two agrochemical actives
dc.typeArticle
dc.identifier.urnURN:NBN:fi:jyu-2011111511684
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.identifier.doi10.1039/C1CE05730H
dc.date.updated2011-11-15T04:30:10Z
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.format.pagerange6531-6537
dc.relation.issn1466-8033
dc.relation.numberinseries21
dc.relation.volume13
dc.type.versionacceptedVersion
dc.rights.copyright© The Royal Society of Chemistry 2011. This is an electronic final draft version of an article whose final and definitive form has been published in CrystEngComm by RSC.
dc.rights.accesslevelopenAccessfi


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