Search results for "metallophthalocyanines"
showing 3 items of 3 documents
Hybrid TiO2 @ phthalocyanine catalysts in photooxidation of 4-nitrophenol: Effect of the matrix and sensitizer type
2020
Abstract Microcrystalline and nanocrystalline anatase (TiO2) based hybrid photocatalysts including selected phthalocyanine sensitizers were explored in photooxidation of 4-nitrophenol (4-NP) in water. Composites obtained with the homemade pure nano-anatase displayed a very poor catalytic performance compared to the other ones prepared from the commercial Tioxide-Huntsman (micro) and Evonik P25 (nano) products. In particular, the microcrystalline anatase impregnated with sandwich phthalocyanines of Gd or Yb showed excellent results both in photooxidation of 4-NP and hydroquinone, and proved the only ones which completely removed these two compounds from the system during the same reaction cy…
Examples of UV–Vis profiles use as tool for evidence of the metallophthalocyanines transformation
2017
Abstract The UV–Vis spectra for a set of MPcs (Mmetal, Pc = phthalocyanine ligand), i.e.: In(III)PcI (1), Hf(IV)PcI2Pht (Pht = phthalonitrile) (2), Sn(II)Pc (3), Sn(IV)PcI2 (4), and Ge(IV)PcI2 (5) have been examined in two solvents, O-donative acetylacetone, and non-coordinative benzene. The UV–Vis spectra in Hacac solution of 1,2 and 4,5 shows that the axially ligated iodine atoms are replaced by (acac)− anions of the solvent, whereas in 3 the oxygen donors of the solvent causing the auto-oxidation of Sn(II) to Sn(IV) ions and as a result the Sn(II)Pc is transformed into the Sn(IV)Pc(acac)2. The chloride complexes of the 1–5 compounds are formed at Hacac solution after acidification by hyd…
Cobalt, copper and zinc octacarboxyphthalocyanine activity in anaerobic oxidation of -SH group containing compounds
2007
Wykonano serię pomiarów elektrochemicznych w celu określenia aktywności katalitycznej oktakarboksyftalocyjaniny kobaltu, cynku i miedzi w anaerobowym utlenianiu związków organicznych zawierających grupę-SH. Badano następujące substraty: 2-tioetanol (TE), L-cysteinę i 1,4-ditio-2,3-butanodiol (DTT). Jako elektrodę wskaźnikową stosowano elektrodę grafitową GE. Przeprowadzono badania dla roztworów substratów, w których potencjalny katalizator był rozpuszczony, jak i dla roztworów, w których katalizator był zaadsorbowany na powierzchni elektrody GE. Jedynie oktakarboksyftalocyjanina kobaltu, CoPcOC, zaadsorbowana na powierzchni elektrody grafitowej okazała się dobrym katalizatorem heterogennym.…