The fluorescence spectra in cyclohexane of a series of benzanilides(BAs) with different \%para\% substituents at the anilino moiety revealed that BAs emitted dual fluorescence, with one normal weak emission at ca . 33...
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The fluorescence spectra in cyclohexane of a series of benzanilides(BAs) with different \%para\% substituents at the anilino moiety revealed that BAs emitted dual fluorescence, with one normal weak emission at ca . 330 nm and an abnormally long wavelength emission ranging from 460 to 550 nm. The long wavelength emission was found strongly dependent of the electron donating capacity of the substituent at the anilino moiety and a stronger electron donating substituent led to a red shift in the emission. The energies of the long wavelength emission of the BAs were correlated to the oxidation potentials of the donors, E \-\{D/D +\}, and a nice linear correlation was found with a slope of +0 66, which clearly pointed to the charge transfer character of the emissive state for the long wavelength emission and the high decoupling extent of the charges in the CT state. This is the first report that shows the direct evidence for the CT nature. The results might be of significance in understanding the photophysics of peptide and protein and in designing novel fluorescent chemosensors.
Dual fluorescence at ca . 447 nm and 545 nm was observed from the aqueous 1 naphthylamine (NA) solutions at pH higher than 13 6. Similar dual fluorescence was also found with sodium 1 naphthylaminoacetate(NAA) , but n...
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Dual fluorescence at ca . 447 nm and 545 nm was observed from the aqueous 1 naphthylamine (NA) solutions at pH higher than 13 6. Similar dual fluorescence was also found with sodium 1 naphthylaminoacetate(NAA) , but not with N, N disubstituted 1 aminonaphthalenes such as sodium 1 naphthylaminodiacetate(NADA) and 1 dimethylaminonaphthalene(DMAN). No change in absorption spectra of NA and NAA was observed in this pH *** was proposed that the dual fluorescence observed with NA and NAA was due to the excited state dissociation of the primary and secondary amines at high pH. From the dual fluorescence intensity ratio pH titration curve, the p K * as of NA and NAA were estimated to be between 14 and 15 which are much lower than the ground state p K a. The novel approatch is such a simple, convenient and frequent analysis technique that it can be widely used in detecting the substitutional derivatives of aminonaphthalene.
A novel reserved\|phase ion\|pair liquid chromatographic method using hexadecyltrimethylammonium bromide（HTMAB） as an ion\|pair reagent for separating the complexes of metal and 8\|hydroxyquinoline\|5\|sulphonic aci...
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A novel reserved\|phase ion\|pair liquid chromatographic method using hexadecyltrimethylammonium bromide（HTMAB） as an ion\|pair reagent for separating the complexes of metal and 8\|hydroxyquinoline\|5\|sulphonic acid（HQS） coupled with on\|line fluorescence detection has been developed. The chromatographic behavior of metal\|HQS complexes in the proposed system was systematically *** the C\-\{18\} column modified by HTMAB and the suitable mobile phase coupled with fluorescence detection（\%λ\%\-\{ex\}=388 nm; \%λ\%\-\{em\}=518 nm） were employed, the detection limit of cadmium is 7.72 ng/mL with an injection volume of 20 μL, and the linear range of calibration curve for cadmium is 50\800 ng/mL. It was successfully applied to determination of bio\|available cadmium in polluted soils of China. Moreover, the possible species of Cd\|HQS on the column has been investigated by log\|log plot analysis.
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