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Author

Lin Zhong

Bio: Lin Zhong is an academic researcher from University of Science and Technology of China. The author has contributed to research in topics: Triphosgene & Diphosgene. The author has an hindex of 3, co-authored 3 publications receiving 101 citations.
Topics: Triphosgene, Diphosgene, Fluorophore, Phosgene

Papers
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Journal ArticleDOI
TL;DR: A ratiometric fluorescent chemosensor, Phos-1, was constructed with 4,5-diaminonaphthalimide as a fluorophore for selective and visual detection of phosgene.

80 citations

Journal ArticleDOI
TL;DR: A new 1,8-naphthalimide-based fluorescent chemosensor, Phos-2, which exhibits high sensitivity, high selectivity to phosgene and its substitutes over nitric oxide (NO), various acyl chlorides, and nerve agent mimics in solutions is developed.
Abstract: Phosgene and its substitutes, diphosgene and triphosgene, are highly toxic and widely used chemicals, so it is necessary to investigate their reactivity and develop facile, sensitive, and specific methods for detecting them. In this work, we have developed a new 1,8-naphthalimide-based fluorescent chemosensor, Phos-2, which exhibits high sensitivity (detection limits: 0.2-0.7 nm), high selectivity to phosgene and its substitutes over nitric oxide (NO), various acyl chlorides, and nerve agent mimics in solutions. Based on investigation of the reaction kinetics of Phos-2 with phosgene and its substitutes, a two-step sensing mechanism was clarified. The second-order rate constants (k2 ) of Phos-2 reveal that the relative rate constants of phosgene, diphosgene, and triphosgene are 40:4:1. Moreover, a Phos-2 test paper has been fabricated as a low-cost, sensitive (≈5 ppm from observation by the naked eye or 0.1 ppm from a measurement), and efficient method for visual detection of a low concentration of phosgene in the gas phase.

51 citations

Journal ArticleDOI
TL;DR: In this paper, four diethylaminoquinoline derivatives with different 2-vinyl substituents have been constructed for the detection of CN−/HCN via a Michael addition.
Abstract: Cyanide ion (CN−) is highly toxic, and its wide use in industry poses an immediate threat to public safety. Consequently, it is desired to develop reliable and facile methods to detect this dangerous chemical. In this work, four diethylaminoquinoline derivatives (3a–3d) with different 2-vinyl substituents have been constructed for the detection of CN−/HCN via a Michael addition. The electrophilicity of the β-carbon of 2-vinyl group depends on the electron-withdrawing ability of the substituents, which tune the photophysical properties of sensors and sensing products by varying intramolecular charge transfer (ICT). Among these sensors, 3a displays the best sensing behavior towards CN−, that is, rapid colorimetric and ratiometric fluorescent response (∼10 s), high sensitivity (LOD = 15 nM) and high selectivity in solutions. The sensing mechanism of a two-step reaction has been clearly demonstrated by 1H NMR, HRMS and tracking and titration experiments. Moreover, the test strip with 3a has been fabricated with a polyethyl oxide and successfully applied to detect HCN gas (60 ppm) visually and selectively.

17 citations


Cited by
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Journal ArticleDOI
TL;DR: This review describes in a comprehensive manner recent progress that has been made on the development of chromophore-based chemosensors for detecting nerve agents (mimic) and phosgene.
Abstract: The extreme toxicity and ready accessibility of nerve agents and phosgene has caused an increase in the demand to develop effective systems for the detection of these substances. Among the traditional platforms utilized for this purpose, chemosensors including surface acoustic wave (SAW) sensors, enzymes, carbon nanotubes, nanoparticles, and chromophore based sensors have attracted increasing attention. In this review, we describe in a comprehensive manner recent progress that has been made on the development of chromophore-based chemosensors for detecting nerve agents (mimic) and phosgene. This review comprises two sections focusing on studies of the development of chemosensors for nerve agents (mimic) and phosgene. In each of the sections, the discussion follows a format which concentrates on different reaction sites/mechanisms involved in the sensing processes. Finally, chemosensors uncovered in these efforts are compared with those based on other sensing methods and challenges facing the design of mor...

172 citations

Journal ArticleDOI
TL;DR: In this paper, the most significant developments in fluorescent probes for the detection of the carbonyl species formaldehyde, carbon monoxide and phosgene in recent years, with a special emphasis on their mechanisms and applications.

133 citations

Journal ArticleDOI
TL;DR: A highly selective fluorescent sensor o-Pab for phosgene with a BODIPY unit as a fluorophore and o-phenylenediamine as a reactive site is constructed and excellent discrimination of o- Pab has been demonstrated to be due to the difference in highly reactive and bifunctional phosGene relative to its substitutes.
Abstract: As a highly toxic and widely used chemical, phosgene has become a serious threat to humankind and public security because of its potential use by terrorists and unexpected release during industrial accidents. For this reason, it is an urgent need to develop facile, fast, and selective detection methods of phosgene. In this Article, we have constructed a highly selective fluorescent sensor o-Pab for phosgene with a BODIPY unit as a fluorophore and o-phenylenediamine as a reactive site. The sensor o-Pab exhibits rapid response (∼15 s) in both colorimetric and turn-on fluorescence modes, high selectivity for phosgene over nerve agent mimics and various acyl chlorides and a low detection limit (2.7 nM) in solutions. In contrast to most undistinguishable sensors reported, o-Pab can react with phosgene but not with its substitutes, triphosgene and biphosgene. The excellent discrimination of o-Pab has been demonstrated to be due to the difference in highly reactive and bifunctional phosgene relative to its subst...

107 citations

Journal ArticleDOI
TL;DR: A colorimetric and ratiometric fluorescence probe 1 for phosgene has been developed based on an ESIPT process as mentioned in this paper, which can be easily observed by the naked eye.
Abstract: Phosgene is a highly toxic substance that has become a serious potential threat to public health safety. A colorimetric and ratiometric fluorescence probe 1 for phosgene has been developed based on an ESIPT process. Both the visible colorimetric change from colorless to yellow and the fluorescent color change from blue to green (under 365 nm hand-held UV lamp) can be easily observed by the naked eye. Probe 1 has a high sensitivity and selectivity for phosgene in solutions and the gas phase. The mechanism for sensing by 1 was investigated by using high-resolution mass spectrometry and 1H NMR and 13C NMR spectroscopies.

92 citations

Journal ArticleDOI
TL;DR: A fluorescent chemosensor has been developed for discriminative detection of phosgene and a nerve agent mimic diethyl chlorophosphate (DCP), which was comprised of an anthracene-carboxyimide fluorophore and o-phenylenediamine reaction site.
Abstract: A fluorescent chemosensor has been developed for discriminative detection of phosgene and a nerve agent mimic diethyl chlorophosphate (DCP), which was comprised of an anthracene-carboxyimide fluorophore and o-phenylenediamine (OPD) reaction site. Upon phosphorylation of OPD, the chemosensor displays an obvious fluorescence turn-on response toward DPC at 588 nm with instant response and a low detection limit (88 nM). By contrast, the chemosensor exhibits a colorimetric and fluorescence enhancement response at 500 nm toward phosgene with fast response (<2 min), high selectivity, and a low detection limit (72 nM). Furthermore, chemosensor-loaded test membrane was fabricated for real-time, portable and efficient discriminative detection of trace amounts of gaseous phosgene and DCP vapor with different optical responses.

82 citations