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IRIS è il sistema di gestione della ricerca dell’Università degli Studi di Milano-Bicocca.Il repository BOA è il modulo del sistema dedicato alla raccolta e alla disseminazione della produzione scientifica di Ateneo. Le pubblicazioni sono ricercabili per parola chiave attraverso il box nella barra orizzontale in alto oppure, mediante il pulsante Sfoglia, per "Afferenza", "Autore", "Titolo", "Tipologia" o "Settore scientifico-disciplinare".
IRIS contiene inoltre alcuni moduli dedicati alla registrazione dei progetti e dei contratti, e alla reportistica avanzata per le attività di valutazione della ricerca
EnglishThe synthesis and characterization of a hexanuclear cobalt complex 1 involving a non-heme ligand system, L1, supported on a Sn6O6 stannoxane core are reported. Complex 1 acts as a unique catalyst for dioxygen reduction, whose selectivity can be changed from a preferential 4e(-)/4H(+) dioxygen-reduction (to water) to a 2e(-)/2H(+) process (to hydrogen peroxide) only by increasing the temperature from -50 (o)C to 25 (o)C. A variety of spectroscopic methods ((119)Sn-NMR, Magnetic circular dichroism (MCD), electron paramagnetic resonance (EPR), SQUID, UV-Vis absorption, resonance Raman (rRaman), and X-ray absorption spectroscopy (XAS) ) coupled with advanced theoretical calculations has been applied for the unambiguous assignment of the geometric and electronic structure of 1. The mechanism of the O2-reduction reaction has been clarified based on kinetic studies on the overall catalytic reaction as well as each step in the catalytic cycle and by low-temperature detection of intermediates. The O2-binding to 1 results in the efficient formation of a stable end-on μ-1,2-peroxodicobalt(III) intermediate 2 at -50 (o)C, followed by a proton-coupled electron-transfer (PCET) reduction to complete the O(2)-to-2H2O cata-lytic conversion in an overall 4e(-)/4H(+) step. In contrast, at higher temperatures (> 20 oC) the constraints provided by the stannoxane core, makes 2 unstable against a preferential proton-transfer (PT) step, leading to the generation of H2O2 by a 2e(-)/2H(+) process. The present study provides deep mechanistic insight into the dioxygen reduction process that should serve as useful and broadly applicable principles for future design of more efficient catalysts in fuel cells
Monte Pérez, I., Kundu, S., Chandra, A., Craigo, K., Chernev, P., Kuhlmann, U., et al. (2017). Temperature Dependence of the Catalytic Two- versus Four-Electron Reduction of Dioxygen by a Hexanuclear Cobalt Complex. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 139(42), 15033-15042.
| Citazione: | Monte Pérez, I., Kundu, S., Chandra, A., Craigo, K., Chernev, P., Kuhlmann, U., et al. (2017). Temperature Dependence of the Catalytic Two- versus Four-Electron Reduction of Dioxygen by a Hexanuclear Cobalt Complex. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 139(42), 15033-15042. |
| Tipo: | Articolo in rivista - Articolo scientifico |
| Carattere della pubblicazione: | Scientifica |
| Presenza di un coautore afferente ad Istituzioni straniere: | Si |
| Titolo: | Temperature Dependence of the Catalytic Two- versus Four-Electron Reduction of Dioxygen by a Hexanuclear Cobalt Complex |
| Autori: | Monte Pérez, I; Kundu, S; Chandra, A; Craigo, K; Chernev, P; Kuhlmann, U; Dau, H; Hildebrandt, P; Greco, C; Van Stappen, C; Lehnert, N; Ray, K |
| Autori: | |
| Data di pubblicazione: | 2017 |
| Lingua: | English |
| Rivista: | JOURNAL OF THE AMERICAN CHEMICAL SOCIETY |
| Digital Object Identifier (DOI): | http://dx.doi.org/10.1021/jacs.7b07127 |
| Appare nelle tipologie: | 01 - Articolo su rivista |
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