Activation and Transformation of Methane on Boron-Doped Cobalt Oxide Cluster Cations CoBO 2 .
Ming WangFeng-Xiang ZhangZhi-Ying ChenJia-Bi MaPublished in: Inorganic chemistry (2024)
The cleavage of inert C-H bonds in methane at room temperature and the subsequent conversion into value-added products are quite challenging. Herein, the reactivity of boron-doped cobalt oxide cluster cations CoBO 2 + toward methane under thermal collision conditions was studied by mass spectrometry experiments and quantum-chemical calculations. In this reaction, one H atom and the CH 3 unit of methane were transformed separately to generate the product metaboric acid (HBO 2 ) and one CoCH 3 + ion, respectively. Theoretical calculations strongly suggest that a catalytic cycle can be completed by the recovery of CoBO 2 + through the reaction of CoCH 3 + with sodium perborate (NaBO 3 ), and this reaction generates sodium methoxide (CH 3 ONa) as the other value-added product. This study shows that boron-doped cobalt oxide species are highly reactive to facilitate thermal methane transformation and may open a way to develop more effective approaches for methane (CH 4 ) activation and conversion under mild conditions.
Keyphrases
- room temperature
- anaerobic digestion
- ionic liquid
- molecular dynamics
- carbon dioxide
- metal organic framework
- quantum dots
- mass spectrometry
- density functional theory
- highly efficient
- molecular dynamics simulations
- high resolution
- electron transfer
- monte carlo
- visible light
- gold nanoparticles
- ms ms
- dna binding
- capillary electrophoresis
- transcription factor
- simultaneous determination