The complexes of [M(PPh3)2L]X (M = Pd, Co; L = substituted quinoline, bipyridine and phenanthroline, and X = Cl, Br or Clod) have been found to be an electrocatalyst for the reduction of CO1 in acetonitrile (AN) and AN-water (8% for volume) solutions containing 0.1 M tetraethylammonium perchlorate (
Electrocatalytic reduction of carbon dioxide by substituted pyridine and pyrazole complexes of palladium
โ Scribed by A.G.M.Mostafa Hossain; T. Nagaoka; K. Ogura
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 780 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
A series of [PdCI,L,] complexes (L = substituted pyridine and pyrazole) has been tried as an electrocatalyst for the reduction of CO, in acetonitrile (AN) containing 0.1 M tetraethylammonium perchlorate (TEAP) at glassy carbon or Pt electrodes. The complexes working as the catalyst were [PdCI,L,] (L = Pyrazole (Pyra), 4-Methylpyridine (4-Mpy) and 3-methylpyrazole (3-Mpyra)
) at an applied potential of -l.lOV vs Ag/lOmM Ag+ and the reduction products were formic acid and H, with no CO. The current efficiency for the formation of formic acid were 10, 20 and 10.2% for Pd complexes of Pyra, 4-Mpy and 3-Mpyra, respectively. The current efficiency for the hydrogen evolution were 31-54'S, and the source of the formate proton and hydrogen was from the added water (4% by volume).
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