{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T11:36:18Z","timestamp":1785411378993,"version":"3.56.0"},"reference-count":16,"publisher":"International Union of Crystallography (IUCr)","issue":"5","license":[{"start":{"date-parts":[[2026,5,29]],"date-time":"2026-05-29T00:00:00Z","timestamp":1780012800000},"content-version":"vor","delay-in-days":1,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"},{"start":{"date-parts":[[2026,5,29]],"date-time":"2026-05-29T00:00:00Z","timestamp":1780012800000},"content-version":"tdm","delay-in-days":1,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"}],"funder":[{"name":"MESRSand DGRSDT"}],"content-domain":{"domain":["iucr.org","wiley.com","iucrj.org"],"crossmark-restriction":true},"short-container-title":["IUCrData","IUCr Data","International Union Crystallogr Data","Int Union Cryst Data"],"accepted":{"date-parts":[[2026,5,25]]},"published-print":{"date-parts":[[2026,5,28]]},"abstract":"<jats:p>\n                    The title compound, C\n                    <jats:sub>14<\/jats:sub>\n                    H\n                    <jats:sub>12<\/jats:sub>\n                    ClNO\n                    <jats:sub>3<\/jats:sub>\n                    (\n                    <jats:bold>I<\/jats:bold>\n                    ), was obtained from the reaction of 2-amino-4-chloro phenol with vanillin (4-hydroxy-3-methoxybenzaldehyde). It crystallizes with two conformationally different molecules in the asymmetric unit. In one of the molecules, the 4-chloro-2(methyleneamino)phenol moiety is partially positionally disordered with the refined occupancies being 0.850\u2005(2):0.150\u2005(2). In both molecules there are intramolecular O\u2014H...O and O\u2014H...N hydrogen bonds, all enclosing\n                    <jats:italic>S<\/jats:italic>\n                    (5) ring motifs. The configuration about the azomethine bond is\n                    <jats:italic>E<\/jats:italic>\n                    in both molecules. The extended structure features O\u2014H...O, C\u2014H...Cl, C\u2014H...O hydrogen bonds, as well as C\u2014H...\u03c0 and parallel displaced \u03c0\u2013\u03c0 interactions, which lead to the formation of a three-dimensional network.\n                  <\/jats:p>","DOI":"10.1107\/s2414314626005523","type":"journal-article","created":{"date-parts":[[2026,5,27]],"date-time":"2026-05-27T07:49:14Z","timestamp":1779868154000},"update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":0,"title":["(\n                    <i>E<\/i>\n                    )-4-Chloro-2-[(4-hydroxy-3-methoxybenzylidene)amino]phenol"],"prefix":"10.1107","volume":"11","author":[{"given":"Amel","family":"Marir","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yamina","family":"Boudinar","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ouafa","family":"Boukhemis","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amel","family":"Djedouani","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Erwann","family":"Jeanneau","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/029brtt94","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9960-3869","authenticated-orcid":true,"given":"Helen","family":"Stoeckli-Evans","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"329","published-online":{"date-parts":[[2026,5,29]]},"reference":[{"key":"hb4564_bb1","doi-asserted-by":"crossref","first-page":"339","DOI":"10.1107\/S0021889808042726","volume":"42","author":"Dolomanov","year":"2009","journal-title":"J. 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