2020
DOI: 10.1016/j.dyepig.2020.108279
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Iridium(Ⅲ) complex-based phosphorescent probe for rapid, specific, and sensitive detection of phosgene

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Cited by 27 publications
(12 citation statements)
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“…Further, Ma et al . developed a weak phosphorescence probe Ir−OXIME [121] . The oxime converted to nitrile functional groups in the presence of phosgene, leading to the strong phosphorescence property (figure 11C).…”
Section: Activity‐based Fluorescent Probe For Reactive Mono Carbonylsmentioning
confidence: 99%
See 1 more Smart Citation
“…Further, Ma et al . developed a weak phosphorescence probe Ir−OXIME [121] . The oxime converted to nitrile functional groups in the presence of phosgene, leading to the strong phosphorescence property (figure 11C).…”
Section: Activity‐based Fluorescent Probe For Reactive Mono Carbonylsmentioning
confidence: 99%
“…Further, Ma et al developed a weak phosphorescence probe IrÀ OXIME. [121] The oxime converted to nitrile functional groups in the presence of phosgene, leading to the strong phosphorescence property (figure 11C). The probe was excellent considering faster response (< 5 s), high selectivity and very low LOD (2.4 nM).…”
Section: Phosgene (Cocl 2 )mentioning
confidence: 99%
“…Based on this mechanism, carbonyl groups of several uorophores have been substituted with the oxime group, creating feeble "push-pull" based photocaged uorophores with weak uorescence. The resulting oxime-caged uorophores have been used for the detection of diverse chemicals, including hypochlorous acid/ hypochlorite, [50][51][52][53][54][55] phosgene, 56,57 ions, [58][59][60] NO 2 , 61 trichloroisocyanuric acid, 62 and organophosphorous nerve agents. 63 The basis for most of these detections is a deoximation reaction that occurs in the presence of oxidizing agents.…”
Section: Introductionmentioning
confidence: 99%
“…Due to their low cost, specificity, high sensitivity, and ease of use, many fluorescent probes for phosgene have been reported [5] with two nucleophilic groups as the active site for the reaction, o ‐diamine (including one amine plus one o ‐aromatic nitrogen), [6a–y] one amine plus one o ‐hydroxy group, [7a–c] o ‐dihydroxy [8] group and others, [9a–l] and summarized in Table S1 in the Supporting Information. Among the largest class of probes, with o ‐phenylenediamine as the active site, would produce a similar fluorescence response to nitric oxide (NO), [6e, f] which induces o ‐phenylenediamine to form benzotriazole [10] …”
Section: Introductionmentioning
confidence: 99%