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dc.contributor.authorCui, Wei-Rong
dc.contributor.authorLi, Ya-Jie
dc.contributor.authorJiang, Qiao-Qiao
dc.contributor.authorWu, Qiong
dc.contributor.authorLiang, Ru-Ping
dc.contributor.authorLuo, Qiu-Xia
dc.contributor.authorZhang, Li
dc.contributor.authorLiu, Juewen
dc.contributor.authorQiu, Jian-Ding
dc.date.accessioned2022-01-28 20:59:16 (GMT)
dc.date.available2022-01-28 20:59:16 (GMT)
dc.date.issued2021-10
dc.identifier.urihttps://doi.org/10.1016/j.xcrp.2021.100630
dc.identifier.urihttp://hdl.handle.net/10012/18010
dc.description.abstractIt is hard to find new electrochemiluminescence (ECL) luminophores using existing research strategies, especially from ECL non-active monomers. Here, fully conjugated covalent organic frameworks with trithiophene (BTT-COFs) are found to have ultra-high ECL efficiencies (up to 62.2%), even in water and without exogenous co-reactants. Quantum chemistry calculations confirm that the periodic BTT-COFs arrays promote intramolecular electron transfer generating ECL from non-ECL monomers. Modulation of ECL performance is possible by substituting the monomers for those with different electron-withdrawing properties. In addition, the cyano group weaved in the skeleton provides the dense sites for post-functionalization. As a typical use case, a highly selective ECL probe for uranyl ions is reported. The tunable ECL luminophore family possesses a broader development space than the traditional emitters, demonstrates the prospects of ECL-COFs, and affords an idea for detecting various contaminants through the rational design of target ligands.en
dc.description.sponsorshipNational Natural Science Foundation of Chinaen
dc.language.isoenen
dc.publisherElsevieren
dc.relation.ispartofseriesCell Reports Physical Science;
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectcovalent organic frameworksen
dc.subjectelectrochemiluminescenceen
dc.subjecturanyl ionsen
dc.subjectaqueous mediumen
dc.subjectintramolecular charge transferen
dc.titleTunable covalent organic framework electrochemiluminescence from non-electroluminescent monomersen
dc.typeArticleen
dcterms.bibliographicCitationCui, W.-R., Li, Y.-J., Jiang, Q.-Q., Wu, Q., Liang, R.-P., Luo, Q.-X., Zhang, L., Liu, J., & Qiu, J.-D. (2021). Tunable covalent organic framework electrochemiluminescence from non-electroluminescent monomers. Cell Reports Physical Science, 100630. https://doi.org/10.1016/j.xcrp.2021.100630en
uws.contributor.affiliation1Faculty of Scienceen
uws.contributor.affiliation2Chemistryen
uws.contributor.affiliation2Waterloo Institute for Nanotechnology (WIN)en
uws.typeOfResourceTexten
uws.peerReviewStatusRevieweden
uws.scholarLevelFacultyen


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