Spontaneously Self‐Assembled Naphthalimide Nanosheets: Aggregation‐Induced Emission and Unveiling a‐PET for Sensitive Detection of Organic Volatile Contaminants in Water

A simple design strategy of long alkyl chain substitution was formulated to block the detrimental π–π interaction that potentially transforms the aggregation‐caused quenching (ACQ) chromophores into aggregation‐induced emission (AIE) active smart nanomaterials. The long octadecyl pendant chain subst...

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Veröffentlicht in:Angewandte Chemie International Edition 2018-07, Vol.57 (28), p.8488-8492
Hauptverfasser: Meher, Niranjan, Iyer, Parameswar Krishnan
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Sprache:eng
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Zusammenfassung:A simple design strategy of long alkyl chain substitution was formulated to block the detrimental π–π interaction that potentially transforms the aggregation‐caused quenching (ACQ) chromophores into aggregation‐induced emission (AIE) active smart nanomaterials. The long octadecyl pendant chain substituted naphthalimide (NI) derivatives self‐assembled into fluorescent nanosheets (NS)‐like structures that spontaneously have surfaces coated with NI cores in water. The fluorescent NS were subsequently used to recognize the organic volatile contaminants (OVCs) at ppb levels via an acceptor‐excited photoinduced electron transfer (a‐PET) mechanism, unveiled as the first representative example. A new design strategy is thereby provided to detect toxic xylene derivatives in water using smart nanomaterials. A strategically simple non‐conjugated pendant chain was introduced in a classical ACQphoric core to generate fluorescent nanosheets with AIEgenic properties. The spontaneously self‐assembled nano‐assembly was employed for the sensitive detection of toxic organic volatile contaminants (OVCs) unveiling the acceptor‐excited photoinduced electron transfer (a‐PET)‐based sensing mechanism in water.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201802842