Unpolished specimens with a more developed surface have lower color stability. Specimens stored in water develop some changes in their visual appearance. The presently proposed methods are effective in evaluating the luminescence of dental materials. Luminescence needs to be tested in addition to color, as the two characteristics are uncorrelated. It is important to further improve the color and luminescence stability of dental materials.

Experimental time-resolved spectral and photon counting kinetic results confirm formation of an isoalloxazinic excited state via excited-state double proton transfer (ESDPT) catalyzed by a carboxylic acid molecule that forms a hydrogen-bond complex with the parent alloxazine molecule. This isoalloxazinic tautomer manifests itself as a distinct long-lived emissive species formed only in such alloxazine derivatives that were not substituted at the N1 nitrogen atom, being a product of the excited-state reaction occurring from the alloxazinic excited state. Theoretical calculations support the idea that the ESDPT occurs by the concerted mechanism. The calculated activation barrier in the excited state is much lower than the same barrier in the ground state and even disappears for the HOMO-1 to LUMO excitation, which explains the fact that the reaction takes place in the excited-state only. The reaction rate estimated from the emission kinetics is ca. 1.4 x 10(8) dm3 mol(-1) s(-1) in ethanolic solutions of lumichrome with added acetic acid.

No abstract

Quantum chemical density functional theory (DFT) calculations and spectral data were employed to investigate the possibility of the excited-state double proton transfer (ESDPT) in lumichrome crystals. The calculations in a lumichrome dimer predict a transfer of a proton in the first excited state, leading to a cation-anion pair. The presently reported X-ray structure of 1,3-dimethyllumichrome and its complex solid-state luminescence indicate that also in this molecule intermolecular hydrogen bonds might be involved in the photophysics. The long-wavelength emission in lumichrome crystals peaked at 530 nm is attributed to excited-state proton transfer, whereas a wider emission band in methylated lumichrome derivatives peaked at 560 nm is attributed to ions formed upon photoexcitation of the crystals.

No abstract

No abstract

No abstract

The effects of thermomechanical pulp (TMP) bleaching with hydrogen peroxide under acidic and alkaline conditions were studied using different spectroscopic analytical methods. The results of hydroxyl radical determination in bleaching solutions, analyses of carbonyl and carboxyl groups contents in the pulp, and the cellulose fiber surface analysis by X-ray photoelectron spectroscopy (XPS) elucidate the chemistry of the hydrogen peroxide treatment. Diffuse reflectance laser flash photolysis (DRLFP) method showed the differences in the photochemical behavior that reflect the changes of the chromophoric system after the preliminary peroxide bleaching stage under acidic conditions. Fourier transform infrared (FTIR) spectroscopy confirmed the non-delignifying character of the bleaching process. Suppression of carbonyl and formation of carboxyl groups in the case of the two-stage peroxide bleaching performed in the presence of catalysts and stabilizers was also confirmed. FT-Raman studies showed the removal of coniferaldehyde groups after treatment under acidic and alkaline conditions.