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Highly selective oxidation of 3,7-dichloro-8-dichloro methyl quinoline toward quinclorac by CoPc-Mn-Br catalytic system.
- Source :
-
Fuel . Sep2024:Part B, Vol. 371, pN.PAG-N.PAG. 1p. - Publication Year :
- 2024
-
Abstract
- • CoPc-Mn(OAc) 2 -HBr catalytic system for selective oxidation shows high quinclorac selectivity and yield. • CoPc leads to more active species of Co3+, and thus facilitating the catalytic performance. • Experiments and theoretical calculations have proven the generation of 3,7-dichloro quinoline-CO radical species. • A Co2+/Co3+ mediated free radical mechanism is proposed. Nowadays, the use of quinoline derived synthons as precursors of quinclorac products is an important research topic in green chemistry. O 2 is a cheap, stable, and eco-friendly oxidant, holding promise for organic oxidation reactions. Herein, we have pioneered the discovery of CoPc-Mn(OAc) 2 -HBr (CoPc-Mn-Br) catalyst system for the selective oxidation of 3,7-dichloro-8-dichloro methyl quinoline (3,7-D-8-DMQ) into quinclorac with high 3,7-D-8-DMQ conversion at 59.3 %. The CoPc-Mn-Br exhibits excellent selectivity of quinclorac (up to 60.3 %), affording high quinclorac yield of 35.7 %, which is 3.1-fold higher than the yield of Co(OAc) 2 -Mn(OAc) 2 -HBr (Co-Mn-Br). Electron paramagnetic resonance (EPR) investigations and density functional theory (DFT) calculations indicate that CoPc promotes the adsorption and activation of O 2 in this oxidation process, which generates more Co3+, leading to producing the reactive intermediate species 3,7-dichloro-8-carbonyl quinoline free radicals via the radical process. The insight achieved from this fundamental study may be further applied to other organic syntheses via selective oxidation. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00162361
- Volume :
- 371
- Database :
- Academic Search Index
- Journal :
- Fuel
- Publication Type :
- Academic Journal
- Accession number :
- 177845644
- Full Text :
- https://doi.org/10.1016/j.fuel.2024.132120