2005
DOI: 10.1016/j.aca.2005.04.053
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Study of the luminescence behavior of seven quinolones on a paper substrate

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Cited by 9 publications
(5 citation statements)
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“…Levofloxacin is a commercial fluorinated quinolone derivative that exhibits green phosphorescence because of the presence of a nitrogen heterocyclic structure. [ 11 ] The CDs were synthesized by the hydrothermal treatment of levofloxacin, which is expected to preserve the phosphorescence property of levofloxacin. In brief, levofloxacin (0.1 g) and deionized water (40 mL) were heated at 200 °C for 6 h in an autoclave and then cooled to room temperature.…”
Section: Figurementioning
confidence: 99%
“…Levofloxacin is a commercial fluorinated quinolone derivative that exhibits green phosphorescence because of the presence of a nitrogen heterocyclic structure. [ 11 ] The CDs were synthesized by the hydrothermal treatment of levofloxacin, which is expected to preserve the phosphorescence property of levofloxacin. In brief, levofloxacin (0.1 g) and deionized water (40 mL) were heated at 200 °C for 6 h in an autoclave and then cooled to room temperature.…”
Section: Figurementioning
confidence: 99%
“…[11] Thereby, discrepancies described in the literature for the ET of FQs can be understood considering that changes of medium polarity or proticity as well as the temperature considerably modify their ET values. [11,[14][15][16][17][18][19][20][21] Moreover, concentration changes of the amphoteric compounds also produces ET changes do to their self-associations in aqueous medium.…”
Section: Discussionmentioning
confidence: 99%
“…[11][12][13] Nev-ertheless, there are relevant discrepancies in the literature about the energies of 3 FQs using this technique as well as by theoretical methods or analysing energy transfer reactions in laser flash photolysis studies. [11,[14][15][16][17][18][19][20][21] With this background, low-temperature phosphorescence measurements were performed with FQs (CPX, NFX, PFX, ENX, OFX) and other structurally simplest quinolone derivatives such as NLA, pipemidic and piromicic acids (PPA, PRA respectively, see structures in Chart 1) to explore emission changes due to their expected self-associations. Moreover, it was also tried to shed some light on the relevant discrepancies about the energies of 3 FQs, [11,[14][15][16][17][18][19][20][21] which are crucial for the understanding of the photomutagenic properties associated with these drugs.…”
Section: Introductionmentioning
confidence: 99%
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“…Several groups have engaged in modulating and promoting the afterglow performance of FQs. For example, Aucélio’s and Dong’s groups reported the promotion RTP of FQs through coordination with Th (IV) and Cd (II), respectively. , Qu’s group modulated the RTP properties of levofloxacin by processing it into carbon dots through hydrothermal treatment . However, these strategies suffered from dependence on heavy/toxic metal ions or complicated synthesis processes, which were not suitable for developing chemical assays.…”
Section: Introductionmentioning
confidence: 99%