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dc.contributor.authorSalorinne, Kirsi
dc.contributor.authorTero, Tiia-Riikka
dc.contributor.authorLahtinen, Tanja
dc.date.accessioned2016-02-01T06:23:46Z
dc.date.available2016-02-01T06:23:46Z
dc.date.issued2014
dc.identifier.citationSalorinne, K., Tero, T.-R., & Lahtinen, T. (2014). 4,4-Difluoro-2,3;5,6-bis(tetramethylene)-4-bora-3a,4a-diaza-s-indacene (LD540). <em>Acta Crystallographica Section E : Structure Reports Online</em>, 70 (1), o74. <a href="http://dx.doi.org/10.1107/S1600536813033448">doi:10.1107/S1600536813033448</a>
dc.identifier.otherTUTKAID_58680
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/48548
dc.description.abstractThe title compound, C18H21BF2N2, is a lipophilic dye based on a BODIPY fluorophore backbone, which was developed for microscopic imaging of lipid droplets; the molecule has a planar BODIPY core [dihedral angle between the pyrrole rings = 2.3 (3)] and two tetramethylene substituents at the 2,3- and 5,6-positions in a half-chair conformation. One of the tetramethylene substituents is disordered over two two sets of sites with site occupancies of 0.5. In the crystal, pairs of C— HF interactions link the molecules into inversion dimers. Neighbouring dimers are linked by further C—HF interactions, forming an infinite array. C—H and – [centroid–centroid distance = 4.360 (3) A˚ ] interactions are observed between the BODIPY core and the tetramethylene substituents of neighbouring dimer pairs.
dc.language.isoeng
dc.publisherInternational Union of Crystallography
dc.relation.ispartofseriesActa Crystallographica Section E : Structure Reports Online
dc.subject.otherLD540
dc.subject.otherBODIPY
dc.subject.otherlipofiilinen väriaine
dc.subject.otheryksikideröntgendiffraktiotutkimus
dc.subject.otherBODIBY
dc.subject.otherlipophilic dye
dc.subject.othersingle-crystal X-ray study
dc.title4,4-Difluoro-2,3;5,6-bis(tetramethylene)-4-bora-3a,4a-diaza-s-indacene (LD540)
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201602011360
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineFysikaalinen kemia
dc.contributor.oppiaineOrgaaninen kemia
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2016-02-01T04:15:08Z
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.format.pagerangeo74
dc.relation.issn1600-5368
dc.relation.volume70
dc.type.versionpublishedVersion
dc.rights.copyright© the Authors, 2014. This is an open access article published by IUCr.
dc.rights.accesslevelopenAccessfi
dc.relation.doi10.1107/S1600536813033448


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