2001
DOI: 10.1016/s0143-7208(00)00108-x
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Chloride sensitive probes for biological applications

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Cited by 16 publications
(12 citation statements)
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“…The change in the electronic properties and the geometry at the boron atom induces the fluorescence spectral changes of the probes. It is well-known that the quinine/quinoline compounds exhibit high quantum yields in acidic media, from the corresponding quaternized salt [46,47]. Similarly here, the boronic acid probes are more fluorescent in acidic solutions.…”
Section: Photophysical Characterization Of the Quinolinium Probesmentioning
confidence: 54%
See 1 more Smart Citation
“…The change in the electronic properties and the geometry at the boron atom induces the fluorescence spectral changes of the probes. It is well-known that the quinine/quinoline compounds exhibit high quantum yields in acidic media, from the corresponding quaternized salt [46,47]. Similarly here, the boronic acid probes are more fluorescent in acidic solutions.…”
Section: Photophysical Characterization Of the Quinolinium Probesmentioning
confidence: 54%
“…Table I shows the quantum yield values for the probes in water, obtained from a spectral comparison with N -(3-Sulfopropyl)-6-methoxyquinolinium [(SPQ) ( f = 0.53 in water [46])], where we can see that the BMOQBA probes have significantly larger quantum yields as compared to the BMQBA probes. Another reference compound, N -methyl-6-methylquinolinium bromide (MMQ) previously published by the authors [47] exhibits very similar spectral properties, except for a noticeable quantum yield and mean lifetime difference, approximately 10-fold higher than its methyl quinolinium counterpart, namely BMQBA. This indicates an interaction between the phenyl ring and quinolinium moiety for the BMQBA and BMQ probes, Table I, which is not present, or present to a much lesser extent, for the BMOQBA probes.…”
Section: Discussionmentioning
confidence: 99%
“…The change in the electronic properties and the geometry at the boron atom induces the fluorescence spectral changes of the probes. It is well-known that the quinine/quinoline compounds exhibit high quantum yields in acidic media, from the corresponding quatemized salt [46,47]. Similarly here, the boronic acid probes are more fluorescent in acidic solutions.…”
Section: Photophysical Characterization Of the Quinolinium Probesmentioning
confidence: 56%
“…Table 15.2 shows the quantum yield values for the probes in water, obtained from a spectral comparison with iV-(3-sulfopropyl)-6-methoxyquinolinium [ (SPQ) (Of = 0.53 in water [46])], where we can see that the BMOQBA probes have significantly higher quantum yields as compared to the BMQBA probes. Another reference compound, A^-methyl-6-methylquinolinium bromide (MMQ) previously published by the authors [47] exhibits very similar spectral properties to that of BMQ and BMQBA probes, except for a noticeable quantum yield and mean lifetime difference, approximately 10-fold higher than its methyl quinolinium counterpart, namely BMQBA. This indicates an interaction between the phenyl ring and methylquinolinium moiety of the BMQBA and BMQ probes.…”
Section: Glucose Sensing Probes Based On the Quiniloinium Moietymentioning
confidence: 97%
“…Secondly, it is well known that quinolinium derivatives exhibit higher fluorescence intensities over the parent quinolines. This is because, in the parent quinolines, the low-lying triplet n-7i* state deactivates the excited fluorophores, considerably [55][56][57]. Upon quartemization, i.e.…”
Section: Signaling Mechanism In Quinolinium Probesmentioning
confidence: 99%