2017
DOI: 10.1016/j.snb.2017.03.170
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Pyrenyl benzimidazole-isoquinolinones: Aggregation-induced emission enhancement property and application as TNT fluorescent sensor

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Cited by 24 publications
(13 citation statements)
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“…So far, paper-based optical chemical sensors for neutral molecules, anions and cations, relying on benzimidazole derivatives as recognition element, have been successfully presented by several research groups. For example, Boonsri et al demonstrated paper-based sensors for the trinitrotoluene (TNT) detection [74]. Sensing material prepared from pyrene-substituted benzimidazole-isoquinolinones can readily detect TNT in aqueous media by a naked-eye observation at concentrations as low as 50 μM.…”
Section: Other Benzimidazole-based Materials For Optical Sensingmentioning
confidence: 99%
“…So far, paper-based optical chemical sensors for neutral molecules, anions and cations, relying on benzimidazole derivatives as recognition element, have been successfully presented by several research groups. For example, Boonsri et al demonstrated paper-based sensors for the trinitrotoluene (TNT) detection [74]. Sensing material prepared from pyrene-substituted benzimidazole-isoquinolinones can readily detect TNT in aqueous media by a naked-eye observation at concentrations as low as 50 μM.…”
Section: Other Benzimidazole-based Materials For Optical Sensingmentioning
confidence: 99%
“…Nevertheless, the main limitation of colorimetry is low sensitivity and interference by the food sample matrix. Fluorescence detection achieves the quantification of the target by measuring the intensity of the light emitted after the fluorescent substance is irradiated by a laser with an appropriate wavelength . Nowadays, portable commercial detection equipment and mobile cameras can realize accurate fluorescence intensity analysis, making fluorescence detection more popular.…”
Section: Overview Of μPadsmentioning
confidence: 99%
“…Even after nearly four decades of its discovery, it is applied in pharmaceutical, sensors and polymer industry. [4][5][6] The reasons why this reaction enjoys overwhelming success as the key part of the modern chemistry toolbox include the ease with which organoboron reagents are crosscoupled with aryl or heteroaryl halides with high predictability, operational-simplicity, and tolerance for a large number of groups and substituents. [7] In addition, it also offers the advantages, which include: (i) easy availability of organoboron compounds which are thermally stable and inert to oxygen and many solvents including water; (ii) low toxicity of starting materials and by-products; (iii) relatively milder reaction conditions (iv) production of different aryl derivatives high yield and selectivity.…”
Section: Introductionmentioning
confidence: 99%
“…It has been studied more than Stille coupling, Heck coupling, Negishi coupling, Liebeskind‐Srogl coupling, Kharash coupling, Kumuda coupling and Himaya coupling. Even after nearly four decades of its discovery, it is applied in pharmaceutical, sensors and polymer industry [4–6] . The reasons why this reaction enjoys overwhelming success as the key part of the modern chemistry toolbox include the ease with which organoboron reagents are cross‐coupled with aryl or heteroaryl halides with high predictability, operational‐simplicity, and tolerance for a large number of groups and substituents [7] .…”
Section: Introductionmentioning
confidence: 99%