RESUMO
OBJECTIVE: This paper studies the kinetics and mechanism of the sensitized photodegradation of 5-sulfaminouracil (SFU). This compound is a synthetic bacteriostatic belonging to the sulfa drugs, usually detected in surface water and effluent wastewater. METHODS: SFU interacts with electronically excited singlet and triplet states of riboflavin (Rf), (1)Rf* and (3)Rf*, respectively. The rate constants for these processes were determined in MeOH-H2O by stationary fluorescence spectroscopy (for kQ(1)) and by laser flash photolysis (for kQ(3)). RESULTS: SFU is photodegraded by visible light irradiation in the presence of the natural sensitizer (Rf). In competitive processes, (3)Rf* generates the reactive oxygen species superoxide radical anion (O2(â¢-)) and singlet molecular oxygen [O2((1)Δg)], which are involved in SFU photodegradation. In aqueous solutions, where SFU adopts different forms depending on the pH of the medium, the participation of O2((1)Δg) is predominant. Therefore, the O2((1)Δg)-mediated mechanism was evaluated at pHs 7 and 12, employing perinaphthenone as a synthetic photosensitizer. DISCUSSION: The results indicate that SFU is photodegraded through a relatively efficient process in a neutral environment, whereas it is quickly degraded in alkaline media. This is attributed to the ionization of the sulfamino- group, a substituent in the uracil molecule that exerts an activating power on the molecule. Thus, sensitized photodegradation may be an important tool to reduce the environmental impact of SFU.
Assuntos
Antibacterianos/química , Riboflavina/química , Sulfonamidas/química , Uracila/análogos & derivados , Uracila/química , Ânions , Interações Medicamentosas , Radicais Livres , Humanos , Luz , Oxigênio/química , Fotólise , Fármacos Fotossensibilizantes/química , Espécies Reativas de Oxigênio , Espectrometria de FluorescênciaRESUMO
Spectral and photophysical properties of the alkaloid berberine (B) were studied in solvents with different solvent parameters, using UV/Vis absorption, emission and excitation spectroscopy. The absorption and emission maxima were found to be between 421-431 nm and 514-555 nm, respectively, leading to Stokes' shifts between 4099 and 5735 cm(-1). The fluorescence quantum yields varied between 10(-2)-10(-4), depending on the solvent. Different solvent scales have been used to study the solvatochromism of B. Linear solvation energy relationships (LSER) proposed by Kamlet-Taft suggest that B is a molecule attractive as a probe for solvent polarity and hydrogen bonding properties.