2022
DOI: 10.1016/j.dyepig.2022.110673
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A naphthalimide-based fluorescent probe for quantitative sensing of UV light

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Cited by 8 publications
(4 citation statements)
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“…After 10 s of UV irradiation at a low intensity of 0.5 mw/cm 2 , a clear color change from yellow to cyan blue was observed. A response was observed with a UV irradiance intensity as low as 0.1 μW/cm 2 (Figure S24), which is comparable to commercialized UV light radiation devices, lower than that reported for ultraviolet light detection materials. ,, The color-saturated samples of Zn-MOFs-1–5 were completely decolored after being kept in the dark for 9, 28, 41, 25, and 47 h at room temperature, respectively (Figure S25). This reversible color conversion could be repeated three times without a significant color loss.…”
Section: Results and Discussionmentioning
confidence: 69%
See 1 more Smart Citation
“…After 10 s of UV irradiation at a low intensity of 0.5 mw/cm 2 , a clear color change from yellow to cyan blue was observed. A response was observed with a UV irradiance intensity as low as 0.1 μW/cm 2 (Figure S24), which is comparable to commercialized UV light radiation devices, lower than that reported for ultraviolet light detection materials. ,, The color-saturated samples of Zn-MOFs-1–5 were completely decolored after being kept in the dark for 9, 28, 41, 25, and 47 h at room temperature, respectively (Figure S25). This reversible color conversion could be repeated three times without a significant color loss.…”
Section: Results and Discussionmentioning
confidence: 69%
“…Upon UV light irradiation, the UV–vis spectra showed new strong bands centered at 627–751 nm (Figures S43–S47), while the ESR spectra showed stronger and symmetric single-peak radical signals, confirming the existence of photogenerated radicals (Figures S48–S52). ,, For Zn-MOFs-1, 3, and 4, the shortest distances between the O of carboxylate groups and the N of the pyridinium unit were 3.48, 3.83, and 3.56 Å, respectively, satisfying the photoinduced electron paths. The shorter distances are more favorable for electron transfer.…”
Section: Results and Discussionmentioning
confidence: 82%
“…Efficient fluorophores such as coumarin and naphthylimide have also been utilized. 23 Therefore, Li's team synthesized novel caging dyes NPE-HCCC2/AM 15 c and CCC-1 4 b based on coumarin. These dyes exhibit a fairly high quantum yield ( Q = 6000 M −1 cm −1 ) and emit bright blue and green fluorescence upon 365 nm photoactivation.…”
Section: Pafs and Their Applicationsmentioning
confidence: 99%
“…Chen et al developed the novel photocage 8 containing glycine-linked naphthalimide and o-nitrobenzyl groups (Figure 5). [19] Upon irradiation, 8 releases a fluorescent naphthalimide derivative through different routes shown in Figure 5. The released fluorescence intensity is linearly correlated with the intensity of UV irradiation.…”
Section: Of 20mentioning
confidence: 99%