{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,19]],"date-time":"2026-03-19T12:57:24Z","timestamp":1773925044779,"version":"3.50.1"},"reference-count":45,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2026,2,4]],"date-time":"2026-02-04T00:00:00Z","timestamp":1770163200000},"content-version":"vor","delay-in-days":3,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,2,1]],"date-time":"2026-02-01T00:00:00Z","timestamp":1769904000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["Grant 22561021"],"award-info":[{"award-number":["Grant 22561021"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["chemistry-europe.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["ChemPlusChem"],"published-print":{"date-parts":[[2026,2]]},"abstract":"<jats:p>\n                    Various benzene and heterocyclic structures could be connected to both 3,3\u2032\u2010positions of H\n                    <jats:sub>8<\/jats:sub>\n                    \u2010BINOL by Suzuki coupling reactions. The dihedral Angle of H\n                    <jats:sub>8<\/jats:sub>\n                    \u2010BINOL was reduced by the electron\u2010withdrawing groups on the benzene ring, and the dihedral angle was smaller with stronger electron\u2010absorbing ability. Dicyanovinylenes end\u2010capped H\n                    <jats:sub>8<\/jats:sub>\n                    \u2010BINOL derivatives\n                    <jats:bold>R1<\/jats:bold>\n                    have good aggregation\u2010induced emission (AIE) properties and bright yellow fluorescence. The single crystal diffraction pattern manifested that\n                    <jats:bold>R1<\/jats:bold>\n                    molecules exhibited curved ends and could self\u2010assemble into boat\u2010like structures with much smaller dihedral angle of 73.23\u00b0. It was attributed to the formation of molecular torsion due to the electron\u2010withdrawing properties of \u2013CN. The morphology characterization of\n                    <jats:bold>R1<\/jats:bold>\n                    could self\u2010assemble into nanospheres in ethanol solution. The results of fluorescence properties of\n                    <jats:bold>R1<\/jats:bold>\n                    were shown as follows: 1. In DMSO\/H\n                    <jats:sub>2<\/jats:sub>\n                    O system with different proportions,\n                    <jats:bold>R1<\/jats:bold>\n                    had AIE effect, which was attributed to the electron\u2010withdrawing effect of propyl dicyanide. The fluorescence is strongest when the water content is 70%. 2.\n                    <jats:bold>R1<\/jats:bold>\n                    had obvious fluorescence quenching for esomeprazole magnesium and exhibited a low detection limit (LOD\u2009=\u20091.23\u2009\u00d7\u200910\n                    <jats:sup>\u22129<\/jats:sup>\n                    \u2009M), which indicated that the novel fluorescent probe had a good guiding effect on the recognition of chiral drug.\n                  <\/jats:p>","DOI":"10.1002\/cplu.202500715","type":"journal-article","created":{"date-parts":[[2026,2,4]],"date-time":"2026-02-04T16:38:42Z","timestamp":1770223122000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Efficient Detection of Esomeprazole Magnesium Using Self\u2010Assembled Supramolecular of Chiral Dicyanovinylene End\u2010Capped H\n                    <sub>8<\/sub>\n                    \u2010BINOL With AIE Properties"],"prefix":"10.1002","volume":"91","author":[{"given":"Fangxiu","family":"Li","sequence":"first","affiliation":[{"name":"Jiangxi Province Key Laboratory of Organic Functional Molecules Institute of Organic Chemistry Jiangxi Science and Technology Normal University  Nanchang China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zhuhua","family":"Wang","sequence":"additional","affiliation":[{"name":"Jiangxi Province Key Laboratory of Organic Functional Molecules Institute of Organic Chemistry Jiangxi Science and Technology Normal University  Nanchang China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yinghong","family":"Zhou","sequence":"additional","affiliation":[{"name":"Jiangxi Province Key Laboratory of Organic Functional Molecules Institute of Organic Chemistry Jiangxi Science and Technology Normal University  Nanchang 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Nanchang China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7987-6878","authenticated-orcid":false,"given":"Yu","family":"Hu","sequence":"additional","affiliation":[{"name":"College of Chemistry and Chemical Engineering Nanchang University  Nanchang 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