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- W2765659618 abstract "A novel fluorescence chemosensor M1 was designed and synthesized through Knoevenagel condensation reaction between 2-(4-naphthalen-1-yl-phenyl)-2H-[1,2,3]triazole-4-carbaldehyde and malononitrile. UV–vis absorption and fluorescence emission spectroscopy found that M1 possessed intramolecular charge transfer (ICT) and aggregation-induced emission enhancement (AIEE) properties. Because M1 contained dicyano-vinyl groups which can easily occurred the nucleophilic Michael addition of cyanide anion. So M1 exhibited remarkable selectivity and sensitivity toward CN− with a low detection limitation of 3.91 × 10−8 M. The mechanism with cyanide anion was systematically studied by 1H NMR titration experiments and HR-MS." @default.
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- W2765659618 date "2018-03-01" @default.
- W2765659618 modified "2023-10-12" @default.
- W2765659618 title "A novel highly selective probe with both aggregation-induced emission enhancement and intramolecular charge transfer characteristics for CN− detection" @default.
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- W2765659618 doi "https://doi.org/10.1016/j.snb.2017.10.167" @default.
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