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.uri | https://jyx.jyu.fi/handle/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 | journal article | |
dc.identifier.urn | URN:NBN:fi:jyu-201102221796 | |
dc.contributor.laitos | Kemian laitos | fi |
dc.contributor.laitos | Department of Chemistry | en |
dc.contributor.oppiaine | Orgaaninen kemia | fi |
dc.contributor.oppiaine | Organic chemistry | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_6501 | |
dc.description.reviewstatus | peerReviewed | |
dc.relation.issn | 1600-5368 | |
dc.type.version | publishedVersion | |
dc.rights.accesslevel | openAccess | fi |
dc.type.publication | article | |
dc.relation.doi | doi:10.1107/S1600536810024499 | |