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Sustainable transformation of biomass platform molecules to valuable C1 building blocks by selective heterogeneous catalytic oxidation

Subject Area Solid State and Surface Chemistry, Material Synthesis
Organic Molecular Chemistry - Synthesis and Characterisation
Physical Chemistry of Solids and Surfaces, Material Characterisation
Term from 2020 to 2024
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 431189789
 
Final Report Year 2025

Final Report Abstract

We have developed a series of non-noble metal heterogeneous catalysts with isolated CuII active sites such as Cu/5A and Cuphen/C3N4, with bimetal centers such as CuZr/5A, MnO2/Goethite as well as CuAlOx containing Cu2O-Cu interface sites, by ion-exchange, ballmilling, co-precipitation and polycondensation methods. These catalysts have been successfully applied in the selective oxidative valorization of biomass platform molecules derived from glycerol, such as glycerolaldehyde (GLCA), 1,3-dihydroxyacetone (DHA), glycolic acid (GA) and glycolaldehyde (GLA). The following significant progress going beyond the state of the art has been realized: 1) Selective oxidation of DHA to GA and FA at room temperature with very high yields (93 and 83 %, respectively); 2) Use of these platform molecules as carbonyl sources in the selective oxidative N-formylation of amines to formamides with good to excellent yields using H2O2 but also O2 as oxidant; 3) The challenging reductive N-formylation of amines with CO2 and H2 to valuable formamides over a heterogeneous CuAlOx non-noble metal catalyst. Comprehensive characterizations using a multitude of methods such as ICP-AES, XRD, XPS, BET, HAADF-STEM, EELS, NH3-TPD, EPR and XAFS revealed the formation of active sites such as isolated CuII species in Cu/5A and CuZr/5A, single CuN4 sites in Cuphen/C3N4, synergetic interaction between Fe and Mn in MnO2/Goethite and Cu2O-Cu interface sites in CuAlOx, respectively. Reaction mechanism studies by in situ EPR, operando ATR-FTIR experiments and DFT calculations showed that the generation of carbonylcontaining C1 intermediates (FA, C1 radical species) via selective oxidative cleavage of C-C bonds in the biomass-based molecules is vital for formamide formation in the oxidative N- formylation of amines. It has been shown that this reaction is governed by the selective formation of different reactive oxygen species such as ●OH, ●OOH and O2-●. In summary, this project can make a theoretical basis for the understanding of the selective activation and transformation of biomass derivative molecules to synthesize nitrogen-containing fine chemicals, and provide new ideas for valorization of other bio-based platform molecules.

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