ABSTRACT
The immobilization of Re(I) complexes onto metal oxide surfaces presents an elegant strategy to enhance their stability and reusability toward photocatalytic CO2 reduction. In this study, the photocatalytic performance of fac-[ClRe(CO)3(dcbH2)], where dcbH2 = 4,4'-dicarboxylic acid-2,2'-bipyridine, anchored onto the surface of 1%m/m CuO/Nb2O5 was investigated. Following adsorption, the turnover number for CO production (TONCO) in DMF/TEOA increased significantly, from ten in solution to 370 under visible light irradiation, surpassing the TONCO observed for the complex onto pristine Nb2O5 or CuO surfaces. The CuO/Nb2O5 heterostructure allows for efficient electron injection by the Re(I) center, promoting efficient charge separation. At same time CuO clusters introduce a new absorption band above 550 nm that contributes for the photoreduction of the reaction intermediates, leading to a more efficient CO evolution and minimization of side reactions.
ABSTRACT
This study demonstrates in vivo analgesic and anti-inflammatory properties of hydroalcoholic extracts of leaves, bark and flowers from the Handroanthus impetiginosus (Bignoniaceae) plant, recognized as 'Ipê roxo' in Brazil. The extracts were evaluated in male Swiss albino mice via oral administration. Moreover, results of the in vivo paw oedema test induced by carrageenan revealed that extracts of leaves and bark displayed relevant anti-inflammatory activity potential at the dosage of 100 mg/kg, 300 mg/kg, and 500 mg/kg. Likewise, the results obtained for leaves and flowers extracts suggested potent analgesic action in the conventional hot plate test. UPLC/MS analysis of the hydroalcoholic extracts samples identified metabolites belonging to several classes, mainly naphthoquinones and iridoids derivatives as well as flavonoids. Thus, the obtained results indicate that the extracts of H. impetiginosus plant parts could be considered as a complementary herbal medicine for the treatment of pain and inflammation disorders.
ABSTRACT
Black NiO powders were prepared by a hydrothermal method. Moreover, the visible light-driven Ag3PO4/NiO photocatalyst composites were successfully synthesized by in situ precipitation method. These samples were structurally characterized by X-ray diffraction and Rietveld refinement. The strong interaction between the phases and the defects in the samples was affected by the formation of the composites, as identified by Fourier transform infrared spectroscopy and Raman spectroscopy. UV-vis diffuse reflectance spectroscopy exhibited enhanced light absorption for all Ag3PO4/NiO composites, suggesting the effective interaction between the phases. Moreover, field-emission scanning electron microscopy images revealed the presence of NiO microflowers composed of nanoflakes in contact with Ag3PO4 microparticles. The composite with 5% NiO presented enhanced photocatalytic efficiency in comparison with pure Ag3PO4, degrading 96% of rhodamine B (RhB) dye in just 15 min under visible light; however, the recycling experiments confirmed that the composite with 75% NiO showed superior stability. The recombination of the electron-hole pairs was considered for the measurement of the photoluminescence of the samples. These measurements were performed to evaluate the possible causes for the difference in the photocatalytic responses of the composites. From these experimental results, possible photocatalytic mechanisms for RhB degradation over Ag3PO4/NiO composites under visible-light irradiation were proposed.
