{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T11:33:28Z","timestamp":1785411208015,"version":"3.56.0"},"reference-count":16,"publisher":"International Union of Crystallography (IUCr)","issue":"5","license":[{"start":{"date-parts":[[2025,4,8]],"date-time":"2025-04-08T00:00:00Z","timestamp":1744070400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/legalcode"},{"start":{"date-parts":[[2025,4,8]],"date-time":"2025-04-08T00:00:00Z","timestamp":1744070400000},"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":[[2025,4,2]]},"published-print":{"date-parts":[[2025,5,1]]},"abstract":"<jats:p>\n                    In the title compound, C\n                    <jats:sub>15<\/jats:sub>\n                    H\n                    <jats:sub>15<\/jats:sub>\n                    N\n                    <jats:sub>3<\/jats:sub>\n                    O\n                    <jats:sub>2<\/jats:sub>\n                    , (\n                    <jats:bold>I<\/jats:bold>\n                    ), the aniline and phenol rings form a dihedral angle of 62.1\u2005(1)\u00b0. Intermolecular N\u2014H...O and O\u2014H...O hydrogen bonds lead to the formation of sheets extending parallel to (010). Intermolecular interactions were quantified and analysed using Hirshfeld surface analysis, revealing that H...H interactions contribute most to the crystal packing (42.2%). The molecular structure was optimized by density functional theory (DFT) at the B3LYP\/6\u201331\u2005G(d,p) level and was compared with the experimentally determined molecular structure in the solid state.\n                  <\/jats:p>","DOI":"10.1107\/s205698902500297x","type":"journal-article","created":{"date-parts":[[2025,4,7]],"date-time":"2025-04-07T05:46:02Z","timestamp":1744004762000},"page":"389-392","update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":1,"title":["Crystal structure, Hirshfeld surface analysis and DFT studies of 4-amino-\n                    <i>N<\/i>\n                    \u2032-[(1\n                    <i>E<\/i>\n                    )-1-(3-hydroxyphenyl)ethylidene]benzohydrazide"],"prefix":"10.1107","volume":"81","author":[{"given":"Subramani Uma","family":"Maheswari","sequence":"first","affiliation":[{"id":[{"id":"https:\/\/ror.org\/01x24z140","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Srinivasan","family":"Senthilkumar","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":[[2025,4,8]]},"reference":[{"key":"wm5754_bb1","doi-asserted-by":"crossref","first-page":"3019","DOI":"10.1016\/j.ejmech.2010.03.031","volume":"45","author":"Belkheiri","year":"2010","journal-title":"Eur. J. Med. Chem."},{"key":"wm5754_bb2","unstructured":"Bruker (2017). APEX3 and SAINT. Bruker AXS Inc., Madison, Wisconsin, USA."},{"key":"wm5754_bb3","doi-asserted-by":"crossref","first-page":"256","DOI":"10.1107\/S0108768189012929","volume":"46","author":"Etter","year":"1990","journal-title":"Acta Cryst. B"},{"key":"wm5754_bb4","doi-asserted-by":"crossref","first-page":"849","DOI":"10.1107\/S0021889812029111","volume":"45","author":"Farrugia","year":"2012","journal-title":"J. Appl. Cryst."},{"key":"wm5754_bb5","unstructured":"Frisch, M. J., Trucks, G. W., Schlegel, H. B., Scuseria, G. E., Robb, M. A., Cheeseman, J. R., Scalmani, G., Barone, V., Mennucci, B., Petersson, G. A., Nakatsuji, H., Caricato, M., Li, X., Hratchian, H. P., Izmaylov, A. F., Bloino, J., Zheng, G., Sonnenberg, J. L., Hada, M., Ehara, M., Toyota, K., Fukuda, R., Hasegawa, J., Ishida, M., Nakajima, T., Honda, Y., Kitao, O., Nakai, H., Vreven, T., Montgomery, J. A. Jr, Peralta, J. E., Ogliaro, F., Bearpark, M., Heyd, J. J., Brothers, E., Kudin, K. N., Staroverov, V. N., Kobayashi, R., Normand, J., Raghavachari, K., Rendell, A., Burant, J. C., Iyengar, S. S., Tomasi, J., Cossi, M., Rega, N., Millam, J. M., Klene, M., Knox, J. E., Cross, J. B., Bakken, V., Adamo, C., Jaramillo, J., Gomperts, R., Stratmann, R. E., Yazyev, O., Austin, A. J., Cammi, R., Pomelli, C., Ochterski, J. W., Martin, R. L., Morokuma, K., Zakrzewski, V. G., Voth, G. A., Salvador, P., Dannenberg, J. J., Dapprich, S., Daniels, A. D., Farkas, O., Foresman, J. B., Ortiz, J. V., Cioslowski, J. & Fox, D. J. (2009). Gaussian09W. Gaussian Inc., Wallingford, USA."},{"key":"wm5754_bb6","doi-asserted-by":"crossref","first-page":"3616","DOI":"10.1002\/qua.22736","volume":"111","author":"Gulsevensidir","year":"2011","journal-title":"Int. J. 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