(2E,4E,6E)-3-Methyl-7-(pyren-1-yl)octa-2,4,6-trienoic acid

dc.contributor.authorBariamis, S. E.en
dc.contributor.authorMagoulas, G. E.en
dc.contributor.authorAthanassopoulos, C. M.en
dc.contributor.authorPapaioannou, D.en
dc.contributor.authorManos, M. J.en
dc.contributor.authorNastopoulos, V.en
dc.date.accessioned2015-11-24T16:43:04Z
dc.date.available2015-11-24T16:43:04Z
dc.identifier.issn1600-5368-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8643
dc.rightsDefault Licence-
dc.title(2E,4E,6E)-3-Methyl-7-(pyren-1-yl)octa-2,4,6-trienoic aciden
heal.abstractThe title compound, C25H20O2, was synthesized by a Wittig reaction between triphenyl[1-(pyren-1-yl)ethyl]phosphonium bromide and ethyl (2E,4E)-3-methyl-6-oxohexa-2,4-dienoate, in the presence of n-butyl lithium, followed by saponification. It was obtained pure in the all-trans configuration following crystallization from ethyl acetate. The asymmetric unit contains two independent molecules (A and B), which are arranged almost parallel to each other within the crystal structure. The triene chain is not coplanar with the pyrene ring system, forming dihedral angles of 52.8 (1) and 42.2 (1)degrees for molecules A and B, respectively. Intermolecular hydrogen bonds between the carboxyl groups of the molecules link them into centrosymmetric pairs, AA and BB, each with the R-2(2)(8) graph-set motif.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1107/S1600536809038409-
heal.identifier.secondary<Go to ISI>://000270450400327-
heal.identifier.secondaryhttp://journals.iucr.org/e/issues/2009/10/00/fj2242/fj2242.pdf-
heal.journalNameActa Crystallographica Section E-Structure Reports Onlineen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2009-
heal.publisherInternational Union of Crystallographyen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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