{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T12:11:14Z","timestamp":1785413474930,"version":"3.56.0"},"reference-count":17,"publisher":"International Union of Crystallography (IUCr)","issue":"11","license":[{"start":{"date-parts":[[2025,10,9]],"date-time":"2025-10-09T00:00:00Z","timestamp":1759968000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"},{"start":{"date-parts":[[2025,10,9]],"date-time":"2025-10-09T00:00:00Z","timestamp":1759968000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"}],"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":[[2025,10,3]]},"published-print":{"date-parts":[[2025,11,1]]},"abstract":"<jats:p>\n                    The title compound, C\n                    <jats:sub>29<\/jats:sub>\n                    H\n                    <jats:sub>31<\/jats:sub>\n                    NO\n                    <jats:sub>2<\/jats:sub>\n                    , is a multi-substituted piperidine derivative in which the piperidine ring adopts a chair conformation. Intermolecular C\u2014H...O hydrogen bonds as well as C\u2014H...\u03c0 interactions are observed in the crystal, leading to the formation of inversion dimers and chains, respectively. The intermolecular interactions were quantified and analysed using Hirshfeld surface analysis, revealing that H...H interactions contribute the most (70.5%) to the crystal packing.\n                  <\/jats:p>","DOI":"10.1107\/s2056989025008709","type":"journal-article","created":{"date-parts":[[2025,10,6]],"date-time":"2025-10-06T05:58:01Z","timestamp":1759730281000},"page":"1004-1007","update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":0,"title":["Crystal structure and Hirshfeld surface analysis of 1,3,3-trimethyl-2,6-diphenylpiperidin-4-yl 2-phenylprop-2-enoate"],"prefix":"10.1107","volume":"81","author":[{"given":"Aranganathan","family":"Ananthabharathi","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01x24z140","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sekar","family":"Janarthanan","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01x24z140","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mannathusamy","family":"Gopalakrishnan","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01x24z140","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Srinivasan","family":"Pazhamalai","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01x24z140","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sivashanmugam","family":"Selvanayagam","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"329","published-online":{"date-parts":[[2025,10,9]]},"reference":[{"key":"wm5771_bb1","doi-asserted-by":"crossref","first-page":"188","DOI":"10.1186\/s43094-021-00335-y","volume":"7","author":"Abdelshaheed","year":"2021","journal-title":"Future J. 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