2022
DOI: 10.1016/j.jphotochem.2022.114046
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A thiophene based pyrrolo [1, 2-a] quinoxaline fluorescent probe as a “turn-off” sensor for the selective nanomolar detection of sodium ion

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Cited by 9 publications
(5 citation statements)
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“…In order to reveal the quenching mechanism, quenching experiments of the N-CDs@Eu-UiO-66-(COOH) 2 caused by HOCl were conducted at 293 K. Figure C shows that I 0 / I at 440 nm is linear with the concentrations of HOCl, suggesting that both static and dynamic quenching is possible. According to the SV equation, the quenching rate constant ( K q ) was 3.69 × 10 4 L·mol –1 ·s –1 , which was lower than the maximum collision quenching constant of 2.0 × 10 10 L·mol –1 ·s –1 in the dynamic quenching process, indicating that the quenching mechanism belongs to dynamic quenching. To verify the quenching mechanism, transient fluorescence spectra at 440 nm in the absence and presence of HOCl were measured.…”
Section: Resultsmentioning
confidence: 83%
“…In order to reveal the quenching mechanism, quenching experiments of the N-CDs@Eu-UiO-66-(COOH) 2 caused by HOCl were conducted at 293 K. Figure C shows that I 0 / I at 440 nm is linear with the concentrations of HOCl, suggesting that both static and dynamic quenching is possible. According to the SV equation, the quenching rate constant ( K q ) was 3.69 × 10 4 L·mol –1 ·s –1 , which was lower than the maximum collision quenching constant of 2.0 × 10 10 L·mol –1 ·s –1 in the dynamic quenching process, indicating that the quenching mechanism belongs to dynamic quenching. To verify the quenching mechanism, transient fluorescence spectra at 440 nm in the absence and presence of HOCl were measured.…”
Section: Resultsmentioning
confidence: 83%
“…Divya et al developed a novel thiophene based pyrrolo [1,2- a ] quinoxaline fluorescent sensor (TAAPP), which was suitable for the nanomolar detection of sodium ions. 37 The fluorescence quenching mechanism of TAAPP is shown in Fig. 2a.…”
Section: Fluorescent Detection Of Metal Ionsmentioning
confidence: 99%
“…As an important class of nitrogen heterocyclic compounds, pyrrolo[1,2‐ α ]quinoxalines and their derivatives, contain two six‐membered rings and one five‐membered ring in their structures, and have excellent biological activities for compounds containing a pyrrolo[1,2‐ α ]quinoxaline fragment, such as anticancer, [1a] antitumor, antimalarial, [1b] inhibition of protein tyrosine phosphatase 1B, [1c] activation of Sirt2‐7, [1d] inhibition of the D‐ring activity of RAD51, [1e] etc. In addition, the three rings form a highly conjugated plane with large rigidity and exhibit extremely strong fluorescence, [2] and their modification by using different groups can modulate fluorescence of different colors, which can be used in organic electroluminescence, [3] chemical sensing detection, [4] fluorescent probe design, [5] etc, shown in Figure 1, therefore, the rapid construction of pyrrolo[1,2‐ α ]quinoxalines fragment is particularly important.…”
Section: Introductionmentioning
confidence: 99%