1973
DOI: 10.1016/s0003-2670(01)80859-x
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Electronic absorption and fluorescence study of ionization and intramolecular hydrogen-bonding in the α, β-o-hydroxynaphthoic acids

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Cited by 19 publications
(11 citation statements)
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“…The green emission at 540 nm is characteristic of carboxylic groups in their protonated state while the blue emission at 425 nm is due to dissociated carboxylic groups. It is well-known that dissociation of the carboxylic group in aromatic carboxylic acids raises the energy of the first singlet state, causing a blue-shift . In the present experiments the pH of the dispersions was maintained at 4.0.…”
Section: Resultsmentioning
confidence: 89%
See 1 more Smart Citation
“…The green emission at 540 nm is characteristic of carboxylic groups in their protonated state while the blue emission at 425 nm is due to dissociated carboxylic groups. It is well-known that dissociation of the carboxylic group in aromatic carboxylic acids raises the energy of the first singlet state, causing a blue-shift . In the present experiments the pH of the dispersions was maintained at 4.0.…”
Section: Resultsmentioning
confidence: 89%
“…It is well-known that dissociation of the carboxylic group in aromatic carboxylic acids raises the energy of the first singlet state, causing a blueshift. 35 In the present experiments the pH of the dispersions was maintained at 4.0. The green emission band at 540 nm may therefore be identified with acid groups with pK 6.6 that remain protonated at this pH, while the band at 425 nm may be assigned to the dissociated acid groups with pK 4.3.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…The absorption spectrum of NCS-Chrom A, which accounts for 90% of the total UV-absorbing and bioactive material in NCS, has considerable fine structure with band maxima in spectral regions characteristic of various hydroxynaphthoic acids (Schulman & Kovi, 1973): specifically in the regions 230-270 nm and 320-340 nm, where the isolated hydroxynaphthoic acid derivative of NCS-Chrom and its methyl ester (Edo et al, 1980; . A. Napier and I. H. Goldberg, unpublished experiments) absorb.…”
Section: Discussionmentioning
confidence: 99%
“…SM5): 2HBA (k ex = 310 nm, k em = 440 nm), 1H2NA (k ex = 340 nm, k em = 415 nm) and 1,4DH2NA (k ex = 340 nm, k em = 445 nm). These fluorescence emission bands can be assigned to monomers of ligands existing in polar solvents at low concentrations [60][61][62][63]. The emission intensities depend on the protonation of the carboxylate group [64] i.e.…”
Section: Fluorescence Spectramentioning
confidence: 99%