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- ItemRuthenium(II)-bis(4'-(4-ethynylphenyl)-2,2':6', 2''-terpyridine) - A versatile synthon in supramolecular chemistry. Synthesis and characterization(Warsaw : Central European Science Journals, 2011) Siebert, R.; Schlütter, F.; Winter, A.; Presselt, M.; Görls, H.; Schubert, U.S.; Dietzek, B.; Popp, J.A homoleptic ethynyl-substituted ruthenium(II)-bisterpyridine complex representing a versatile synthon in supramolecular chemistry was synthesized and analyzed by NMR spectroscopy, mass spectrometry and X-ray diffractometry. Furthermore, its photophysical properties were detailed by UV/Vis absorption, emission and resonance Raman spectroscopy. In order to place the results obtained in the context of the vast family of ruthenium coordination compounds, two structurally related complexes were investigated accordingly. These reference compounds bear either no or an increased chromophore in the 4̀-position. The spectroscopic investigations reveal a systematic bathochromic shift of the absorption and emission maximum upon increasing chromophore size. This bathochromic shift of the steady state spectra occurs hand in hand with increasing resonance Raman intensities upon excitation of the metal-to-ligand charge-transfer transition. The latter feature is accompanied by an increased excitation delocalization over the chromophore in the 4̀-position of the terpyridine. Thus, the results presented allow for a detailed investigation of the electronic effects of the ethynyl substituent on the metal-to-ligand charge-transfer states in the synthon for click reactions leading to coordination polymers.
- ItemAlZn based Co and Ni catalysts for the partial oxidation of bioethanol - Influence of different synthesis procedures(Warsaw : Central European Science Journals, 2014) Ehrich, H.; Kraleva, E.The catalytic performance of Co and Ni catalysts on AlZn mixed oxide supports depends on the synthesis procedure used for their preparation. For this study CoAlZn and NiAlZn catalysts were prepared by conventional sol-gel synthesis of the mixed oxide and subsequent impregnation of the support with the transition metal (SG = sol gel method) as well as by a single-step method were a gel is formed based on salts of all components using citric acid as chelating agent (CM = citrate method). The structure and morphology of the catalysts were characterized by nitrogen sorption, XRD and TPR measurements. They showed high activity in the partial oxidation of ethanol at 600-750 °C, but their properties depend on the preparation method. The higher performance of the catalysts prepared by the citrate method, where the transition metal is incorporated into the crystal structure of the support during preparation, is based on a change in morphology and structure, resulting in more active sites exposed on the surface. Compared to the Co catalysts, Ni catalysts showed a higher performance. This might be due to the higher reducibility and the smaller Ni particles size, which allows a better interaction with the support in NiAlZn catalysts.
- ItemRemoval of hazardous pharmaceutical from water by photocatalytic treatment(Warsaw : Central European Science Journals, 2010) Choina, J.; Duwensee, H.; Flechsig, G.-U.; Kosslick, H.; Morawski, A.W.; Tuan, V.A.; Schulz, A.The photocatalytic abatement of hazardous pharmaceuticals has been investigated at very low concentration in the ppb range as found in wastewater and in environmental pollutants. Photocatalytic degradation of tetracycline as a model compound with titania catalysts has been studied using solarium UV-A and black light with differentially applied electric power, tetracycline and catalyst concentration. Abatement of up to 90% has been achieved after 1 hour. Adsorption of tetracycline and photochemical degradation contribute significantly to the abatement of tetracycline resulting in an immediate reduction during the initial period of treatment. Contribution of adsorption is high at very low concentration (500 ppb). Photocatalytic treatment with titania is even highly efficient in the abatement of very small concentrations of tetracycline in drinking water. © 2010 Versita Warsaw and Springer-Verlag Wien.