| Literature DB >> 20827690 |
Andrea Božović1, Stefan Feil, Gregory K Koyanagi, Albert A Viggiano, Xinhao Zhang, Maria Schlangen, Helmut Schwarz, Diethard K Bohme.
Abstract
The room-temperature chemical kinetics has been measured for the catalytic activity of Group 10 atomic cations in the oxidation of methane to methanol by ozone. Ni(+) is observed to be the most efficient catalyst. The complete catalytic cycle with Ni(+) is interpreted with a computed potential energy landscape and, in principle, has an infinite turnover number for the oxidation of methane, without poisoning side reactions. The somewhat lower catalytic activity of Pd(+) is reported for the first time and also explored with DFT calculations. Pt(+) is seen to be ineffective as a catalyst because of the observed failure of PtO(+) to convert methane to methanol.Entities:
Year: 2010 PMID: 20827690 DOI: 10.1002/chem.201000627
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236