Phosphine-borane catalysts for CO2 activation and reduction: a computational study

0558547 - ÚOCHB 2023 RIV GB eng J - Článek v odborném periodiku
Kessete, J. M. - Demissie, T. B. - Chilume, M. - Mohammed, A. M. - Andrushchenko, Valery
Phosphine-borane catalysts for CO2 activation and reduction: a computational study.
Molecular Physics. Roč. 120, č. 12 (2022), č. článku e2087566. ISSN 0026-8976. E-ISSN 1362-3028
Výzkumná infrastruktura: e-INFRA CZ - 90140
Institucionální podpora: RVO:61388963
Klíčová slova: phosphine-borane * carbon dioxide reduction * frustrated Lewis pairs * metal-free * DFT calculations
Obor OECD: Physical chemistry
Impakt faktor: 1.7, rok: 2022
Způsob publikování: Omezený přístup
https://doi.org/10.1080/00268976.2022.2087566

CO2 conversion to value-added chemicals requires efficient catalytic CO2 reduction. Activation of CO2 using 14 phosphine-borane frustrated Lewis pair catalysts was done computationally using B3LYP-D3/6-31++G(d,p)/PCM/THF and M06-2X/6-311++G(d,p)/PCM/THF methods. We designed 14 catalysts, 12 of which exhibit better catalytic activity towards CO2 activation. Moreover, the catalytic mechanisms of compounds 12 and 4 were predicted, and they showed an efficient catalytic system for CO2 reduction to CO, HCHO and HCOOH. Catalysts 2, 3 and 4, with the same methylene linker, have activation energies of 20.5, 18.3 and 10.4 kcal/mol, respectively. This indicates that the catalytic activity of the compound is highly influenced by the ligand bound to borane and phosphine. Compound 4 with the CO2 activation energy of 10.4 kcal/mol is the most efficient catalyst for CO2 activation ever reported among phosphine-borane catalysts. The energy barriers for H-2 activation with catalyst 12 (ΔG(double dagger) = 26.6 kcal/mol) and 4 (ΔG(double dagger) = 34.0 kcal/mol) are higher than the HCOOH releasing activation energy. The designed compounds will help to synthesise efficient metal-free phosphine-borane catalysts. Our results also indicate that phosphine-borane catalysts are promising candidates for CO2 reduction and direct hydrogenation.
Trvalý link: http://hdl.handle.net/11104/0332185