{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T09:54:15Z","timestamp":1785405255735,"version":"3.56.0"},"reference-count":17,"publisher":"International Union of Crystallography (IUCr)","issue":"5","license":[{"start":{"date-parts":[[2025,4,24]],"date-time":"2025-04-24T00:00:00Z","timestamp":1745452800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"},{"start":{"date-parts":[[2025,4,24]],"date-time":"2025-04-24T00:00:00Z","timestamp":1745452800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"}],"funder":[{"name":"This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors"}],"content-domain":{"domain":["iucr.org","wiley.com","iucrj.org"],"crossmark-restriction":true},"short-container-title":["Acta Crystallogr E Cryst Commun","Acta Cryst E","Acta Cryst Sect E","Acta Crystallogr E","Acta Crystallogr Sect E","Acta Cryst E Cryst Commun","Acta Cryst Sect E Cryst Commun"],"accepted":{"date-parts":[[2025,4,13]]},"published-print":{"date-parts":[[2025,5,1]]},"abstract":"<jats:p>\n                    In the title compound C\n                    <jats:sub>19<\/jats:sub>\n                    H\n                    <jats:sub>24<\/jats:sub>\n                    N\n                    <jats:sub>2<\/jats:sub>\n                    OS, intermolecular N\u2014H...O hydrogen bonds generate\n                    <jats:italic>R<\/jats:italic>\n                    <jats:sub>2<\/jats:sub>\n                    <jats:sup>2<\/jats:sup>\n                    (8) ring motifs, forming dimers with an interaction energy of \u221270.5\u2005kJ\u2005mol\n                    <jats:sup>\u22121<\/jats:sup>\n                    . A short S...C interaction produces another dimer with an interaction energy of \u221230.6\u2005kJ\u2005mol\n                    <jats:sup>\u22121<\/jats:sup>\n                    . The intermolecular interactions were quantified using Hirshfeld surface analysis. The two-dimensional fingerprint plots indicate that the major contributions to the crystal packing are from H...H (67.9%), C...H (13.7%), O...H (7.3%) and S...H (4.3%) interactions.\n                  <\/jats:p>","DOI":"10.1107\/s2056989025003329","type":"journal-article","created":{"date-parts":[[2025,4,15]],"date-time":"2025-04-15T02:23:56Z","timestamp":1744683836000},"page":"417-419","update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":3,"title":["Crystal structure, Hirshfeld surface analysis and DFT studies of 2-[4-(2-methylpropyl)phenyl]-\n                    <i>N<\/i>\n                    \u2032-[(1\n                    <i>Z<\/i>\n                    )-1-(thiophen-2-yl)ethylidene]propanehydrazide"],"prefix":"10.1107","volume":"81","author":[{"given":"Sarayu","family":"Jayadevan","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K. 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