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Indicators, absorption maxima neutralized indicator solutions

Trans-resveratrol (trans-3,5,4 -trihydroxystilbene) is a non-flavonoid polyphenol found in grapes, mulberries, and other food prod-ucts. It is responsible for the antioxidant activity of red wine. Intake of moderate amount of red wine has been found to reduce the risk of cardiovascular diseases. In addition to antioxidant activity, resveratrol could inhibit platelet aggregation, and showed anticancer activity. The phenoxyl radicals of resveratrol produced during oxidation by hydroxyl radicals, one-electron oxidants, and peroxyl radicals showed absorption maximum at 410 nm (Fig. I). Reports indicate that trans-resveratrol is a better radical scavenger than vitamins E and C and its activity is similar to that of the flavonoids epicatechin and quercetin. From the comparison of the spectral and kinetic properties of the transients derived from trans-resveratrol and its analogues, it could be concluded that in the neutral and acidic solutions, the para-hydroxy... [Pg.581]

Both the visible and X-ray photoelectron spectra of the electro-deposited film indicated that the metal-ring structure of (EtO)ePcZn was maintained in the film. Before these spectral measurements, the film was kept at -0.5 V for 5 min in 0.1 M n-Bu4NC104/dichloromethane solution, for neutralization. Although the peak in the visible spectrum of the film obtained by reflection method was rather broad, the wavelength of the absorption maximum was almost identical to that of an (EtOaPcZn film... [Pg.517]

Fig. 2. The isosbestic points at 446 and 556 nm in the absorption spectra are matched by an isoemissive point at 685 nm indicating only two species present in solution, both of which are emissive. The shift in emission maximum from 606 nm in neutral solutions to 728 nm upon addition of acid may have interesting sensor applications. The results for 4 stand in contrast with results from dppz-containing Ru(II) tris diimine complexes, where dppz = dipyrido-ipyridophenazine, in which reversible protonation of quinoxaline N atoms leads to quenching of emission. Luminescence in frozen solvent glasses for 4 at 77 K is much stronger ( = 0.044 for the qdt complex), but still broad and without resolved structure. Fig. 2. The isosbestic points at 446 and 556 nm in the absorption spectra are matched by an isoemissive point at 685 nm indicating only two species present in solution, both of which are emissive. The shift in emission maximum from 606 nm in neutral solutions to 728 nm upon addition of acid may have interesting sensor applications. The results for 4 stand in contrast with results from dppz-containing Ru(II) tris diimine complexes, where dppz = dipyrido-ipyridophenazine, in which reversible protonation of quinoxaline N atoms leads to quenching of emission. Luminescence in frozen solvent glasses for 4 at 77 K is much stronger (<f> = 0.044 for the qdt complex), but still broad and without resolved structure.

See other pages where Indicators, absorption maxima neutralized indicator solutions is mentioned: [Pg.217]    [Pg.333]    [Pg.353]    [Pg.561]    [Pg.67]    [Pg.220]    [Pg.59]    [Pg.7]    [Pg.89]    [Pg.499]    [Pg.228]    [Pg.283]   
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Absorption indicators

Absorption maximum

Absorption solution

Indicator Solutions

Indicators, absorption maxima

Neutral solutes

Neutral, solutions neutralization

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