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(1S)-1-phenylethanaminium 4-{[(1S,2S)-1-hydroxy-2,3-dihydro-1H,1'H-[2,2'-biinden]-2-yl]methyl}benzoate

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dc.creator Frampton, CS
dc.creator Zhang, T
dc.creator Scalabrino, GA
dc.creator Frankish, N
dc.creator Sheridan, H
dc.date 2014-04-28T10:17:57Z
dc.date 2014-04-28T10:17:57Z
dc.date 2012
dc.date.accessioned 2022-05-25T14:34:02Z
dc.date.available 2022-05-25T14:34:02Z
dc.identifier Acta Crystallographica Section C: Crystal Structure Communications, 68(8), 2012
dc.identifier 0108-2701
dc.identifier http://scripts.iucr.org/cgi-bin/paper?S0108270112031265
dc.identifier http://bura.brunel.ac.uk/handle/2438/8347
dc.identifier http://dx.doi.org/10.1107/S0108270112031265
dc.identifier.uri http://localhost:8080/xmlui/handle/CUHPOERS/171227
dc.description Copyright 2012 © International Union of Crystallography.
dc.description The 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.
dc.language en
dc.publisher International Union of Crystallography
dc.title (1S)-1-phenylethanaminium 4-{[(1S,2S)-1-hydroxy-2,3-dihydro-1H,1'H-[2,2'-biinden]-2-yl]methyl}benzoate
dc.type Article


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