| Autor: |
Shimoda T; Chemistry Division , Brookhaven National Laboratory , Upton , New York 11973-5000 , United States.; Graduate School of Science and Engineering , Saitama University , Saitama , 338-8570 , Japan., Morishima T; Graduate School of Science and Engineering , Saitama University , Saitama , 338-8570 , Japan., Kodama K; Graduate School of Science and Engineering , Saitama University , Saitama , 338-8570 , Japan., Hirose T; Graduate School of Science and Engineering , Saitama University , Saitama , 338-8570 , Japan., Polyansky DE; Chemistry Division , Brookhaven National Laboratory , Upton , New York 11973-5000 , United States., Manbeck GF; Chemistry Division , Brookhaven National Laboratory , Upton , New York 11973-5000 , United States., Muckerman JT; Chemistry Division , Brookhaven National Laboratory , Upton , New York 11973-5000 , United States., Fujita E; Chemistry Division , Brookhaven National Laboratory , Upton , New York 11973-5000 , United States. |
| Abstrakt: |
The cobalt complexes Co II L1(PF 6 ) 2 (1; L1 = 2,6-bis[2-(2,2'-bipyridin-6'-yl)ethyl]pyridine) and Co II L2(PF 6 ) 2 (2; L2 = 2,6-bis[2-(4-methoxy-2,2'-bipyridin-6'-yl)ethyl]pyridine) were synthesized and used for photocatalytic CO 2 reduction in acetonitrile. X-ray structures of complexes 1 and 2 reveal distorted trigonal-bipyramidal geometries with all nitrogen atoms of the ligand coordinated to the Co(II) center, in contrast to the common six-coordinate cobalt complexes with pentadentate polypyridine ligands, where a monodentate solvent completes the coordination sphere. Under electrochemical conditions, the catalytic current for CO 2 reduction was observed near the Co(I/0) redox couple for both complexes 1 and 2 at E 1/2 = -1.77 and -1.85 V versus Ag/AgNO 3 (or -1.86 and -1.94 V vs Fc +/0 ), respectively. Under photochemical conditions with 2 as the catalyst, [Ru(bpy) 3 ] 2+ as a photosensitizer, tri- p-tolylamine (TTA) as a reversible quencher, and triethylamine (TEA) as a sacrificial electron donor, CO and H 2 were produced under visible-light irradiation, despite the endergonic reduction of Co(I) to Co(0) by the photogenerated [Ru(bpy) 3 ] + . However, bulk electrolysis in a wet CH 3 CN solution resulted in the generation of formate as the major product, indicating the facile production of Co(0) and [Co-H] n+ ( n = 1 and 0) under electrochemical conditions. The one-electron-reduced complex 2 reacts with CO to produce [Co 0 L2(CO)] with ν CO = 1894 cm -1 together with [Co II L2] 2+ through a disproportionation reaction in acetonitrile, based on the spectroscopic and electrochemical data. Electrochemistry and time-resolved UV-vis spectroscopy indicate a slow CO binding rate with the [Co I L2] + species, consistent with density functional theory calculations with CoL1 complexes, which predict a large structural change from trigonal-bipyramidal to distorted tetragonal geometry. The reduction of CO 2 is much slower than the photochemical formation of [Ru(bpy) 3 ] + because of the large structural changes, spin flipping in the cobalt catalytic intermediates, and an uphill reaction for the reduction to Co(0) by the photoproduced [Ru(bpy) 3 ] + . |
