Abstract
Quantum chemistry calculations predict that besides the reported single metal anion Pt−, Ni− can also mediate the co-conversion of CO2 and CH4 to form [CH3−M(CO2)−H]– complex, followed by transformation to C−C coupling product [H3CCOO−M−H]− (A), hydrogenation products [H3C−M−OCOH]− (B) and [H3C−M−COOH]−. For Pd−, a fourth product channel leading to PdCO2−…CH4 becomes more competitive. For Ni−, the feed order must be CO2 first, as the weaker donor-acceptor interaction between Ni− and CH4 increases the C−H activation barrier, which is reduced by [Ni−CO2]−. For Ni−/Pt−, the highly exothermic products A and B are similarly stable with submerged barrier that favors B. The smaller barrier difference between A and B for Ni− suggests the C−C coupling product is more competitive in the presence of Ni− than Pt−. The charge redistribution from M− is the driving force for product B channel. This study adds our understanding of single atomic anions to activate CH4 and CO2 simultaneously.
Original language | English |
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Article number | e202200789 |
Journal | ChemPhysChem |
Volume | 24 |
Issue number | 7 |
DOIs | |
Publication status | Published - 3 Apr 2023 |
Keywords
- CH activation
- CO reduction
- C−C coupling
- quantum chemistry calculations
- single metal anion