{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,1,14]],"date-time":"2025-01-14T05:12:36Z","timestamp":1736831556793,"version":"3.33.0"},"reference-count":12,"publisher":"International Union of Crystallography (IUCr)","issue":"2","license":[{"start":{"date-parts":[[2013,1,16]],"date-time":"2013-01-16T00:00:00Z","timestamp":1358294400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/journals.iucr.org\/services\/copyrightpolicy.html"},{"start":{"date-parts":[[2013,1,16]],"date-time":"2013-01-16T00:00:00Z","timestamp":1358294400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/journals.iucr.org\/services\/copyrightpolicy.html#TDM"}],"content-domain":{"domain":["iucr.org","wiley.com","iucrj.org"],"crossmark-restriction":true},"short-container-title":["Acta Crystallogr C Cryst Struct Commun","Acta Cryst C","Acta Cryst Sect C","Acta Crystallogr C","Acta Crystallogr Sect C","Acta Crystallogr Sect C Cryst Struct Commun"],"published-print":{"date-parts":[[2013,2,15]]},"abstract":"<jats:p>The asymmetric unit of the title salt [systematic name: bis(4-(2,3-dichlorophenyl)-1-{4-[(2-oxo-1,2,3,4-tetrahydroquinolin-7-yl)oxy]butyl}piperazin-1-ium) oxalate\u2013oxalic acid (1\/1)], 2C<jats:sub>23<\/jats:sub>H<jats:sub>28<\/jats:sub>Cl<jats:sub>2<\/jats:sub>N<jats:sub>3<\/jats:sub>O<jats:sub>2<\/jats:sub><jats:sup>+<\/jats:sup>\u00b7C<jats:sub>2<\/jats:sub>O<jats:sub>4<\/jats:sub><jats:sup>2\u2212<\/jats:sup>\u00b7C<jats:sub>2<\/jats:sub>H<jats:sub>2<\/jats:sub>O<jats:sub>4<\/jats:sub>, consists of one protonated aripiprazole unit (HArip<jats:sup>+<\/jats:sup>), half an oxalate dianion and half an oxalic acid molecule, the latter two lying on inversion centres. The conformation of the HArip<jats:sup>+<\/jats:sup>cation differs from that in other reported salts and resembles more the conformation of neutral Arip units in reported polymorphs and solvates. The intermolecular interaction linking HArip<jats:sup>+<\/jats:sup>cations is also similar to those in reported Arip compounds crystallizing in the space group<jats:italic>P<\/jats:italic>\\overline{1}, with head-to-head N\u2014H...O hydrogen bonds generating centrosymmetric dimers, which are further organized into planar ribbons parallel to (01\\overline{2}). The oxalate anions and oxalic acid molecules form hydrogen-bonded chains running along [010], which `pierce' the planar ribbons, interacting with them through a number of stronger N\u2014H...O and weaker C\u2014H...O hydrogen bonds, forming a three-dimensional network.<\/jats:p>","DOI":"10.1107\/s0108270113001133","type":"journal-article","created":{"date-parts":[[2013,1,15]],"date-time":"2013-01-15T18:06:13Z","timestamp":1358273173000},"page":"186-190","update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":4,"title":["Aripiprazole salts. III. 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