Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3367
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dc.contributor.authorSingh, Harpreet-
dc.contributor.authorDevi, M.-
dc.contributor.authorIqbal, Mohamed Musthafa-
dc.contributor.authorNailwal, Y.-
dc.contributor.authorPal, S.K.-
dc.date.accessioned2020-12-26T04:54:10Z-
dc.date.available2020-12-26T04:54:10Z-
dc.date.issued2020-
dc.identifier.citationACS Applied Materials and Interfaces 12(11), pp. 13248-13255.en_US
dc.identifier.otherhttps://doi.org/10.1021/acsami.9b20743-
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acsami.9b20743-
dc.identifier.urihttp://hdl.handle.net/123456789/3367-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractThe exfoliation of covalent organic frameworks into covalent organic nanosheets (CONs) not only helps to reduce fluorescence turn-off phenomena but also provides well-exposed active sites for fast response and recovery for various applications. The present work is an example of rational designing of a structure constructed by condensing triaminoguanidinium chloride (TGCl), an intrinsic ionic linker, with a fluorophore, 2, 5-dimethoxyterephthalaldehyde (DA), to produce highly fluorescent self-exfoliable ionic CONs (DATGCl-iCONs). These fluorescent iCONs are able to sense fluoride ions selectively down to the ppb level via the fluorescence turn-off mechanism. A closer look at the quenching mechanism via NMR, zeta potential measurement, lifetime measurement, and density functional theory calculations reveals unique proton-triggered fluorescence switching behavior of newly synthesized DATGCl-iCONs.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectCovalent organic framework (COF)en_US
dc.subjectExfoliationen_US
dc.subjectAnion sensoren_US
dc.subjectNanosheetsen_US
dc.subject2D materialsen_US
dc.subjectGuanidineen_US
dc.titleProton-Triggered Fluorescence Switching in Self-Exfoliated Ionic Covalent Organic Nanosheets for Applications in Selective Detection of Anionsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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