2022
DOI: 10.1016/j.saa.2021.120795
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A dual-response fluorescent probe for discriminative sensing of hydrazine and bisulfite as well as intracellular imaging with different emission

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Cited by 15 publications
(6 citation statements)
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“…To detect toxic analytes, the 1,1,2-trimethyl-1 H -benzo­(e)­indole moiety was mainly used to create a higher wavelength-emitting fluorescent probe. When the benzo-hemicyanine dye was coupled with an electron-donating system, it yields active CN + and CC bonds in conjugation due to the electron-deficient character of the alkylated nitrogen atom. , The active CC double bond is expected to be disconnected (loss of conjugation) by the addition of HS – , resulting in a noticeable blue shift; however, a nonfluorescence emission was observed due to the nucleophilic addition of cyanide to the electron-deficient imine bond on the benzo-hemicyanine moiety. Based on this, we chose the 1,1,2-trimethyl-1 H -benzo­(e)­indole moiety with N -alkylation by the propyl group to avoid interactions of common ions and fused with 4-(methylthio)­benzaldehyde. The presence of the electron-rich sulfur atom in 4-(methylthio)­benzaldehyde and electron-deficient nature of benzo-hemicyanine facilitate donor-π-acceptor (push–pull) interactions between polar CC double bonds.…”
Section: Resultsmentioning
confidence: 99%
“…To detect toxic analytes, the 1,1,2-trimethyl-1 H -benzo­(e)­indole moiety was mainly used to create a higher wavelength-emitting fluorescent probe. When the benzo-hemicyanine dye was coupled with an electron-donating system, it yields active CN + and CC bonds in conjugation due to the electron-deficient character of the alkylated nitrogen atom. , The active CC double bond is expected to be disconnected (loss of conjugation) by the addition of HS – , resulting in a noticeable blue shift; however, a nonfluorescence emission was observed due to the nucleophilic addition of cyanide to the electron-deficient imine bond on the benzo-hemicyanine moiety. Based on this, we chose the 1,1,2-trimethyl-1 H -benzo­(e)­indole moiety with N -alkylation by the propyl group to avoid interactions of common ions and fused with 4-(methylthio)­benzaldehyde. The presence of the electron-rich sulfur atom in 4-(methylthio)­benzaldehyde and electron-deficient nature of benzo-hemicyanine facilitate donor-π-acceptor (push–pull) interactions between polar CC double bonds.…”
Section: Resultsmentioning
confidence: 99%
“…Moreover, these fluorochromes can flow between adjacent membranes, leading to increased fluorescence and false-positive results during evaluation. Dual or discriminative immunofluorescence allows determination of the location where the fluorescence signal is occurring, whether in the cytoplasm, endosome, or another organelle ( Yang et al, 2022 ). However, this approach uses statistical methods to quantify a region observed through the microscope.…”
Section: Discussionmentioning
confidence: 99%
“…7 In order to selectively detect analytes that are important to both ecology and physiology, so far, many research groups have reported ESIPT-based fluorophores. [8][9][10] In the recent past, some examples were reported in judicially designed molecules where two-way double proton transfer sites were incorporated to understand the competitiveness of PT processes. [11][12][13] Some research groups have started to investigate the molecular behaviours and photophysical properties of ESIPT chromophores with an extra competitive proton acceptor site both in the solution and solid phases.…”
Section: Introductionmentioning
confidence: 99%