Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 133, Issue 42, Pages 16930-16937Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja206258x
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Funding
- Fonds der Chemischen Industrie
- Deutsche Forschungsgemeinschaft
- cluster of excellence Unifying Concepts in Catalysis
- Alexander von Humboldt-Stiftung
- Stiftung Stipendien Fonds des Verbandes der Chemischen Industrie
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The oxygen-rich cluster Al2O7+ is generated in the gas phase and investigated with respect to both its structure and its reactivity toward small, inert molecules using Fourier-transform ion cyclotron resonance (FT-ICR) mass spectrometry and DFT-based calculations. Al2O7+ reacts with CH4 under ambient conditions via hydrogen atom transfer (HAT), and with H2O a ligand exchange occurs which gives rise to the evaporation of two O-2 molecules. The resulting product ion Al2O4H2+ is also capable of abstracting a hydrogen atom from both H2O and CH4. As indicated in the H2O/2O(2) ligand exchange and supported by collision-induced dissociation (CID) experiments, two O-2 units constitute structural elements of Al2O7+. Further insight is provided by DFT calculations, performed at the unrestricted B3LYP/TZVP level, and reaction mechanisms are suggested on the basis of both the experimental and theoretical results.
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