{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,7]],"date-time":"2026-09-07T22:31:30Z","timestamp":1788820290586,"version":"build-2803163510"},"reference-count":55,"publisher":"International Union of Crystallography (IUCr)","issue":"8","license":[{"start":{"date-parts":[[2023,7,10]],"date-time":"2023-07-10T00:00:00Z","timestamp":1688947200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/journals.iucr.org\/services\/copyrightpolicy.html"},{"start":{"date-parts":[[2023,7,10]],"date-time":"2023-07-10T00:00:00Z","timestamp":1688947200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/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 Struct Chem","Acta Crystallogr C","Acta Crystallogr C Cryst Struct Commun","Acta Cryst C","Acta Cryst C Struct Chem","Acta Cryst Sect C","Acta Cryst Sect C Struct Chem","Acta Crystallogr Sect C","Acta Crystallogr Sect C Struct Chem","Acta Crystallogr Sect C Cryst Struct Commun"],"accepted":{"date-parts":[[2023,7,3]]},"published-print":{"date-parts":[[2023,8,1]]},"abstract":"<jats:p>\n                    The title Schiff base compound, (\n                    <jats:italic>E<\/jats:italic>\n                    )-2-{[(4-methoxynaphthalen-1-yl)methylidene]amino}-4-methylphenol, C\n                    <jats:sub>19<\/jats:sub>\n                    H\n                    <jats:sub>17<\/jats:sub>\n                    NO\n                    <jats:sub>2<\/jats:sub>\n                    (\n                    <jats:bold>I<\/jats:bold>\n                    ), was synthesized\n                    <jats:italic>via<\/jats:italic>\n                    the reaction of 2-amino-4-methylphenol with 4-methoxynaphthalene-1-carbaldehyde. The structure of\n                    <jats:bold>I<\/jats:bold>\n                    was characterized by NMR, IR and UV\u2013Vis spectroscopies in different solvents. The interatomic contacts in the crystal structure were explored using Hirshfeld surface analysis, which, together with the two-dimensional fingerprint plots, confirm the predominance of dispersion forces in the crystal structure. The molecule of\n                    <jats:bold>I<\/jats:bold>\n                    has a twisted conformation, with the mean plane of the naphthalene ring system being inclined to the plane of the phenol ring by 33.41\u2005(4)\u00b0. In the crystal, molecules are linked by C\u2014H...O hydrogen bonds to form inversion dimers. There are parallel-displaced \u03c0\u2013\u03c0 interactions present, together with C\u2014H...\u03c0 interactions, resulting in the formation of a three-dimensional structure. The anticorrosion potential of\n                    <jats:bold>I<\/jats:bold>\n                    was also investigated using density functional theory (DFT) in the gas phase and in various solvents. The compound was shown to exhibit significant anticorrosion properties for iron and copper. The molecular structure of\n                    <jats:bold>I<\/jats:bold>\n                    was determined by DFT calculations at the M062X\/6-311+g(d) level of theory and compared with the crystallographically determined structure. Local and global reactivity descriptors were computed to predict the reactivity of\n                    <jats:bold>I<\/jats:bold>\n                    . Excellent agreement was observed between the calculated results and the experimental data.\n                  <\/jats:p>","DOI":"10.1107\/s2053229623005867","type":"journal-article","created":{"date-parts":[[2023,7,10]],"date-time":"2023-07-10T11:37:08Z","timestamp":1688989028000},"page":"324-333","update-policy":"https:\/\/doi.org\/10.1107\/cm_01","source":"Crossref","is-referenced-by-count":6,"title":["The synthesis and crystal structure of (\n                    <i>E<\/i>\n                    )-2-{[(4-methoxynaphthalen-1-yl)methylidene]amino}-4-methylphenol: Hirshfeld surface analysis, DFT calculations and anticorrosion studies"],"prefix":"10.1107","volume":"79","author":[{"given":"Ahmed Abderrahim","family":"Yahiaoui","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nadir","family":"Ghichi","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/017wv6808","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-6664-179X","authenticated-orcid":true,"given":"Douniazed","family":"Hannachi","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/02rzqza52","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Bilel","family":"Mezhoud","sequence":"additional","affiliation":[{"id":[{"id":"https:\/\/ror.org\/017wv6808","id-type":"ROR","asserted-by":"publisher"}]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amel","family":"Djedouani","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Khairedine","family":"Kraim","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4763-2764","authenticated-orcid":true,"given":"Aur\u00e9lien","family":"Crochet","sequence":"additional","affiliation":[],"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":[[2023,7,10]]},"reference":[{"key":"zo3036_bb1","first-page":"e202203231","volume":"8","author":"Afshari","year":"2023","journal-title":"Chem. 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