2015
DOI: 10.1016/j.snb.2015.07.031
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Sensitive water-soluble fluorescent chemosensor for chloride based on a bisquinolinium pyridine-dicarboxamide compound

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Cited by 34 publications
(23 citation statements)
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References 60 publications
(54 reference statements)
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“…Due to the strong chemical stability and inert chemical reaction of the chloride ion, there are only a few methods for the detection of the chloride ion based on chemiluminescence and fluorescence spectroscopy (Kim et al, 2017). For example, Han developed a fluorescent probe for the chloride ion using Ag-benzimidazole complexes (Kim et al, 2020), and Bazany-Rodríguez et al (2015) reported a watersoluble fluorescent probe for chloride based on a bisquinolinium pyridine-dicarboxamide compound. However, organic fluorescent probes have the disadvantages of poor stability and low fluorescence intensity, so it is necessary to develop chloride fluorescent probes based on nanomaterials.…”
Section: Introductionmentioning
confidence: 99%
“…Due to the strong chemical stability and inert chemical reaction of the chloride ion, there are only a few methods for the detection of the chloride ion based on chemiluminescence and fluorescence spectroscopy (Kim et al, 2017). For example, Han developed a fluorescent probe for the chloride ion using Ag-benzimidazole complexes (Kim et al, 2020), and Bazany-Rodríguez et al (2015) reported a watersoluble fluorescent probe for chloride based on a bisquinolinium pyridine-dicarboxamide compound. However, organic fluorescent probes have the disadvantages of poor stability and low fluorescence intensity, so it is necessary to develop chloride fluorescent probes based on nanomaterials.…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, the absence of a pre-organization of the contact points decreases its iodide-selectivity and affinity. [92] Organic cationic fluorophores with a charge strongly delocalized such as N-quinoliniums, often have ion pairing association with voluminous anions such as iodide, as a result of the hydrophobic effect, with drastic changes in their fluorescent emission properties, which produces a high iodidesensitivity but low selectivity due to lack of a specific binding site.…”
Section: Discussionmentioning
confidence: 99%
“…Quinoline-based quaternary salts have attracted the attention of researchers in different areas of organic chemistry for their relevant applications such as DNA-intercalators (Mazzoli et al, 2011), fluorescent pH-sensors (Badugu et al, 2005a), fluorescent labels for antibiotics (Zeng et al, 2010), proteins (Hong et al, 2004), heparin (Sauceda et al, 2007), sacharides (Badugu et al, 2005b), fluorescent probes for fluoride and cyanide ions (Badugu et al, 2004) and nucleotides (Dorazco-Gonzá lez et al, 2014). These cationic organic compounds are probably the most used fluorescent sensors for chloride ions in aqueous media (Bazany-Rodríguez et al, 2015) and intracell samples (Baù et al, 2012). On the other hand, benzamide compounds are used as intermediaries for the synthesis of species with biological activity such as 1,4-benzodiazepinones, thiazoles and oxazoles (Majumdar & Ganai, 2011;Majumdar & Ghosh, 2013;Majumdar et al, 2012) and bicyclic Nheterocycles and nitrogen-rich medium-size heterocycles (Mondal et al, 2012;Zeni & Larock, 2006;Ohta et al, 2008;Majumdar et al, 2008;Raju et al, 2009;Evdokimov et al, 2011).…”
Section: Chemical Contextmentioning
confidence: 99%