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dc.contributor.authorOśmiałowski, Borys
dc.contributor.authorValkonen, Arto
dc.contributor.authorChęcińska, Lilianna
dc.date.accessioned2022-02-01T14:12:13Z
dc.date.available2022-02-01T14:12:13Z
dc.date.issued2013
dc.identifier.issn1600-5368
dc.identifier.urihttp://hdl.handle.net/11089/40545
dc.descriptionThe asymmetric unit of the title compound, C14H22N4O2·0.25C6H14·0.5H2O, contains two independent mol­ecules of 2,4-bis­(pivaloyl­amino)­pyrimidine (M) with similar conformations, one water mol­ecule and one-half n-hexane solvent mol­ecule situated on an inversion center. In one independent M mol­ecule, one of the two tert-butyl groups is rotationally disordered between two orientations in a 3:2 ratio. The n-hexane solvent mol­ecule is disordered between two conformations in the same ratio. The water mol­ecule bridges two independent M mol­ecules via O—H⋯O, N—H⋯O and O—H⋯N hydrogen bonds into a 2M·H2O unit, and these units are further linked by N—H⋯N hydrogen bonds into chains running in the [010] direction. Weak C—H⋯O inter­actions are observed between the adjacent chains.pl_PL
dc.description.sponsorshipThe financial support from the National Science Centre in Kraków (grant No. NCN204 356840) is gratefully acknowledged. Academy Professor Kari Rissanen is also gratefully acknowledged for financial support (Academy of Finland grant Nos. 122350, 140718, 265328 and 263256).pl_PL
dc.language.isoenpl_PL
dc.publisherInternational Union of Crystallographypl_PL
dc.relation.ispartofseriesActa Crystallographica Section E: Crystallographic Communications;69
dc.rightsUznanie autorstwa 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectsingle-crystal X-ray studypl_PL
dc.subjectT = 123 Kpl_PL
dc.subjectmean σ(C–C) = 0.006 Åpl_PL
dc.subjectdisorder in main residuepl_PL
dc.subjectR factor = 0.079pl_PL
dc.subjectwR factor = 0.164pl_PL
dc.subjectdata-to-parameter ratio = 14.2pl_PL
dc.titleN-[2-(2,2-Di­methyl­propanamido)­pyrimidin-4-yl]-2,2-di­methyl­propanamide n-hexane 0.25-solvate hemihydratepl_PL
dc.typeArticlepl_PL
dc.page.numbero1617-o1618pl_PL
dc.contributor.authorAffiliationFaculty of Technology and Chemical Engineering, University of Technology and Life Sciences, Seminaryjna 3, PL-85-326 Bydgoszcz, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Chemistrycv5431, University of Jyväskylä, P.O. Box 35, FI-40014 Jyväskylä, Finlandpl_PL
dc.contributor.authorAffiliationStructural Chemistry and Crystallography Group, University of Lodz, Pomorska 163/165, PL-90-236 Łódź, Polandpl_PL
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dc.referencesBurla, M. C., Caliandro, R., Camalli, M., Carrozzini, B., Cascarano, G. L., De Caro, L., Giacovazzo, C., Polidori, G. & Spagna, R. (2005). J. Appl. Cryst. 38, 381–388.pl_PL
dc.referencesCrane, J. D. (2003). Acta Cryst. E59, o1854–o1855.pl_PL
dc.referencesOśmiałowski, B., Kolehmainen, E., Gawinecki, R., Dobosz, R. & Kaupinen, R. (2010). J. Phys. Chem. A, 114, 12881–12887.pl_PL
dc.referencesOśmiałowski, B., Kolehmainen, E., Ikonen, S., Valkonen, A., Kwiatkowski, A., Grela, I. & Haapaniemi, E. (2012). J. Org. Chem. 77, 9609–9619.pl_PL
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dc.referencesSheldrick, G. M. (2004). SADABS. University of Göttingen, Germany.pl_PL
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dc.referencesWestrip, S. P. (2010). J. Appl. Cryst. 43, 920–925.pl_PL
dc.contributor.authorEmaillilach@uni.lodz.plpl_PL
dc.identifier.doi10.1107/S160053681302713X
dc.relation.volume11pl_PL
dc.disciplinenauki chemicznepl_PL


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