(E)-7-(Pyren-1-yl)hept-6-enoic acid

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dc.contributor.author Valkonen, Arto
dc.contributor.author Lahtinen, Tanja
dc.contributor.author Rissanen, Kari
dc.date.accessioned 2011-02-22T08:32:39Z
dc.date.available 2011-02-22T08:32:39Z
dc.date.issued 2010
dc.identifier.citation Valkonen, 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.issn 1600-5368
dc.identifier.uri http://hdl.handle.net/123456789/26577
dc.description.abstract The 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.iso eng
dc.publisher International Union of Crystallography
dc.relation.ispartofseries Acta Crystallographica Section E
dc.title (E)-7-(Pyren-1-yl)hept-6-enoic acid
dc.type Article en
dc.identifier.urn URN:NBN:fi:jyu-201102221796
dc.subject.kota 116
dc.contributor.laitos Kemian laitos fi
dc.contributor.laitos Department of Chemistry en
dc.contributor.oppiaine Organic chemistry en
dc.contributor.oppiaine Orgaaninen kemia fi
dc.type.uri http://purl.org/eprint/type/JournalArticle
dc.identifier.doi doi:10.1107/S1600536810024499
dc.description.version Publisher's PDF
eprint.status http://purl.org/eprint/type/status/PeerReviewed

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