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dc.contributor.authorPlutenko, Maxym O.
dc.contributor.authorLampeka, Rostislav D.
dc.contributor.authorHaukka, Matti
dc.contributor.authorNordlander, Ebbe
dc.date.accessioned2016-02-05T09:53:52Z
dc.date.available2016-02-05T09:53:52Z
dc.date.issued2012
dc.identifier.citationPlutenko, M. O., Lampeka, R. D., Haukka, M., & Nordlander, E. (2012). 2-(3,5-Dimethyl-1H-pyrazol-1-yl)-2-hydroxyimino-N0-[1-(pyridin-2-yl)ethylethylidene]. <i>Acta Crystallographica Section E</i>, <i>E68</i>(12), o3381. <a href="https://doi.org/10.1107/S1600536812045412" target="_blank">https://doi.org/10.1107/S1600536812045412</a>
dc.identifier.otherCONVID_22114022
dc.identifier.otherTUTKAID_54093
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/48639
dc.description.abstractIn the title compound, C14H16N6O2, the dihedral angles formed by the mean plane of the acetohydrazide group [maximum deviation 0.0629 (12) A˚ ] with the pyrazole and pyridine rings are 81.62 (6) and 38.38 (4) respectively. In the crystal, molecules are connected by N—HO and O—HN hydrogen bonds into supramolecular chains extending parallel to the c-axis direction.
dc.language.isoeng
dc.publisherWiley-Blackwell
dc.relation.ispartofseriesActa Crystallographica Section E
dc.relation.urihttp://journals.iucr.org/e/journalhomepage.html
dc.subject.othersingle-crystal X-ray study
dc.subject.otherdihedral angles
dc.subject.otheracetohydrazide group
dc.subject.otherpyridine rings
dc.subject.othersupramolecular chains
dc.title2-(3,5-Dimethyl-1H-pyrazol-1-yl)-2-hydroxyimino-N0-[1-(pyridin-2-yl)ethylethylidene]
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201602041441
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineKemiafi
dc.contributor.oppiaineChemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2016-02-04T10:15:15Z
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.format.pagerangeo3381
dc.relation.issn1600-5368
dc.relation.numberinseries12
dc.relation.volumeE68
dc.type.versionpublishedVersion
dc.rights.copyright© 2012 the Authors. This is an open access article published by International Union of Crystallography & Wiley.
dc.rights.accesslevelopenAccessfi
dc.relation.doi10.1107/S1600536812045412


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