Please use this identifier to cite or link to this item: http://buratest.brunel.ac.uk/handle/2438/8347
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dc.contributor.authorFrampton, CS-
dc.contributor.authorZhang, T-
dc.contributor.authorScalabrino, GA-
dc.contributor.authorFrankish, N-
dc.contributor.authorSheridan, H-
dc.date.accessioned2014-04-28T10:17:57Z-
dc.date.available2014-04-28T10:17:57Z-
dc.date.issued2012-
dc.identifier.citationActa Crystallographica Section C: Crystal Structure Communications, 68(8), 2012en_US
dc.identifier.issn0108-2701-
dc.identifier.urihttp://scripts.iucr.org/cgi-bin/paper?S0108270112031265en
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/8347-
dc.descriptionCopyright 2012 © International Union of Crystallography.en_US
dc.description.abstractThe title molecular salt, C8H12N+·C26H21O3-, contains a dimeric indane pharmacophore that demonstrates potent anti-inflammatory activity. The indane group of the anion exhibits some disorder about the [alpha]-C atom, which appears common to many structures containing this group. A model to account for the slight disorder was attempted, but this was deemed unsuccessful because applying bond-length constraints to all the bonds about the [alpha]-C atom led to instability in the refinement. The absolute configuration was determined crystallographically as S,S,S by anomalous dispersion methods with reference to both the Flack parameter and Bayesian statistics on Bijvoet differences. The configuration was also determined by an a priori knowledge of the absolute configuration of the (1S)-1-phenylethanaminium counter-ion. The molecules pack in the crystal structure to form an infinite two-dimensional hydrogen-bond network in the (100) plane of the unit cell.en_US
dc.language.isoenen_US
dc.publisherInternational Union of Crystallographyen_US
dc.title(1S)-1-phenylethanaminium 4-{[(1S,2S)-1-hydroxy-2,3-dihydro-1H,1'H-[2,2'-biinden]-2-yl]methyl}benzoateen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1107/S0108270112031265-
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