Khalilov, Ali N.Atioğlu, ZelihaAkkurt, MehmetDuruskari, Gulnara Sh.Toze, A. A. FlavienHuseynova, Afet T.2020-06-272020-06-272019KHALİLOV, A. N., ATİOĞLU, Z., AKKURT, M., DURUSKARI, G. S., TOZE, F. A., & HUSEYNOVA, A. T. (2019). Crystal structure and Hirshfeld surface analysis of E 3 4 fluorobenzylidene amino 5 phenylthiazolidin 2 iminium bromide. Acta Crystallographica Section E: Crystallographic Communications, 75(5), 662–666.2056-9890https://hdl.handle.net/20.500.12695/567https://doi.org/10.1107/S2056989019004973TARAMAPUBMEDTARAMASCOPUSTARAMAWOSIn the cation of the title salt, C16H15FN3S+·Br?, the phenyl ring is disordered over two sets of sites with a refined occupancy ratio of 0.503?(4):0.497?(4). The mean plane of the thia­zolidine ring makes dihedral angles of 13.51?(14), 48.6?(3) and 76.5?(3)° with the fluoro­phenyl ring and the major- and minor-disorder components of the phenyl ring, respectively. The central thia­zolidine ring adopts an envelope conformation. In the crystal, centrosymmetrically related cations and anions are linked into dimeric units via N—H...Br hydrogen bonds, which are further connected by weak C—H...Br hydrogen bonds into chains parallel to [110]. Hirshfeld surface analysis and two-dimensional fingerprint plots indicate that the most important contributions to the crystal packing are from H...H (44.3%), Br...H/H...Br (16.8%), C...H/H...C (13.9%), F...H/H...F (10.3%) and S...H/H...S (3.8%) inter­actions.In the cation of the title salt, C16H15FN3S+·Br?, the phenyl ring is disordered over two sets of sites with a refined occupancy ratio of 0.503?(4):0.497?(4). The mean plane of the thia­zolidine ring makes dihedral angles of 13.51?(14), 48.6?(3) and 76.5?(3)° with the fluoro­phenyl ring and the major- and minor-disorder components of the phenyl ring, respectively. The central thia­zolidine ring adopts an envelope conformation. In the crystal, centrosymmetrically related cations and anions are linked into dimeric units via N—H...Br hydrogen bonds, which are further connected by weak C—H...Br hydrogen bonds into chains parallel to [110]. Hirshfeld surface analysis and two-dimensional fingerprint plots indicate that the most important contributions to the crystal packing are from H...H (44.3%), Br...H/H...Br (16.8%), C...H/H...C (13.9%), F...H/H...F (10.3%) and S...H/H...S (3.8%) inter­actions.enAttribution-NonCommercial-ShareAlike 4.0 Internationalinfo:eu-repo/semantics/openAccessCrystal structureCharge assisted hydrogen bondingThia­zolidine ringDisorderHirshfeld surface analysisArticle75566266610.1107/S2056989019004973Q3N/A