Näytä suppeat kuvailutiedot

dc.contributor.authorValkonen, Arto
dc.contributor.authorLahtinen, Tanja
dc.contributor.authorRissanen, Kari
dc.date.accessioned2011-02-22T08:32:39Z
dc.date.available2011-02-22T08:32:39Z
dc.date.issued2010
dc.identifier.citationValkonen, A., Lahtinen, T. & Rissanen, K. (2010). (E)-7-(Pyren-1-yl)hept-6-enoic acid. Acta Crystallographica E, Vol. 66, Issue 7, p. o1837-o1838. doi:10.1107/S1600536810024499.
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/26577
dc.description.abstractThe title compound, C₂₃H₂₀O₂, is a precursor of a pyrene-based supramolecular element for non-covalent attachment to a carbon nanotube. The asymmetric unit contains three independent molecules. The carboxylic acid group in each of these molecules serves as an intermolecular hydrogen-bond donor and acceptor, generating the commonly observed double O-H...O hydrogen-bond motif in an eight-membered ring. Weaker C-H...O, π π [centroid-centroid distance = 3.968 (4) Å] and C-H...π interactions are also found in the crystal structure.
dc.language.isoeng
dc.publisherInternational Union of Crystallography
dc.relation.ispartofseriesActa Crystallographica Section E
dc.title(E)-7-(Pyren-1-yl)hept-6-enoic acid
dc.typeArticle
dc.identifier.urnURN:NBN:fi:jyu-201102221796
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineOrganic chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.identifier.doidoi:10.1107/S1600536810024499
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.relation.issn1600-5368
dc.type.versionpublishedVersion
dc.rights.accesslevelopenAccessfi


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Näytä suppeat kuvailutiedot