{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,21]],"date-time":"2026-01-21T15:01:51Z","timestamp":1769007711967,"version":"3.49.0"},"reference-count":39,"publisher":"Wiley","issue":"57","license":[{"start":{"date-parts":[[2022,8,18]],"date-time":"2022-08-18T00:00:00Z","timestamp":1660780800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["22171165, 21901145"],"award-info":[{"award-number":["22171165, 21901145"]}],"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":["Chemistry A European J"],"published-print":{"date-parts":[[2022,10,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Chirality transfer from chiral molecules to assemblies is of vital importance to the design of functional chiral materials. In this work, selective co\u2010assembly behaviors between chiral molecules and an achiral luminophore, potentially driven by the intermolecular salt\u2010bridge type hydrogen bonds are reported. Cyano\u2010substituted tetrakis(arylthio)benzene carboxylic acid (<jats:bold>TA<\/jats:bold>) served as the luminophore and hydrogen bond donors, which underwent co\u2010assembly with different chiral amines. It was found that structures of chiral amines affect the chirality transfer and the properties of co\u2010assemblies due to effects on hydrogen bonds and stacking pattern. Only in specific co\u2010assemblies, the chiroptical properties occurred at both ground state and excited states based on the emerged Cotton effects and circularly polarized luminescence (CPL) signals, revealing that the chirality was successfully transferred from molecular level to supramolecular level. In addition, accurate quantitative examination of chiral amines was realized by circular dichroism (CD) spectra. This work demonstrates the characteristic chirality response and transfer through co\u2010assembly, providing a potential method to develop smart chiroptical materials.<\/jats:p>","DOI":"10.1002\/chem.202201956","type":"journal-article","created":{"date-parts":[[2022,7,25]],"date-time":"2022-07-25T11:28:51Z","timestamp":1658748531000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":4,"title":["Co\u2010Assembly of Chiral Amines and a Four\u2010Armed Cyano\u2010Substituted Luminophore through Hydrogen Bonds for Potential Development of Smart Chiroptical Materials"],"prefix":"10.1002","volume":"28","author":[{"given":"Yiping","family":"Liu","sequence":"first","affiliation":[{"name":"School of Chemistry and Chemical Engineering Shandong University  Jinan 250100 P. R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aiyou","family":"Hao","sequence":"additional","affiliation":[{"name":"School of Chemistry and Chemical Engineering Shandong University  Jinan 250100 P. R. China"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4302-3846","authenticated-orcid":false,"given":"Pengyao","family":"Xing","sequence":"additional","affiliation":[{"name":"School of Chemistry and Chemical Engineering Shandong University  Jinan 250100 P. R. 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