Hydrogen Borrowing: towards Aliphatic Tertiary Amines from Lignin Model Compounds Using a Supported Copper Catalyst. Issue 19 (24th August 2022)
- Record Type:
- Journal Article
- Title:
- Hydrogen Borrowing: towards Aliphatic Tertiary Amines from Lignin Model Compounds Using a Supported Copper Catalyst. Issue 19 (24th August 2022)
- Main Title:
- Hydrogen Borrowing: towards Aliphatic Tertiary Amines from Lignin Model Compounds Using a Supported Copper Catalyst
- Authors:
- Ruijten, Dieter
Narmon, Thomas
De Weer, Hanne
van der Zweep, Robbe
Poleunis, Claude
Debecker, Damien P.
Maes, Bert U. W.
Sels, Bert F. - Abstract:
- Abstract: Upcoming biorefineries, such as lignin‐first provide renewable aromatics containing unique aliphatic alcohols. In this context, a Cu‐ZrO2 catalyzed hydrogen borrowing approach was established to yield tertiary amine from the lignin model monomer 3‐(3, 4‐dimethoxyphenyl)‐1‐propanol and the actual lignin‐derived monomers, (3‐(4‐hydroxyphenyl)‐1‐propanol and dihydroconiferyl alcohol), with dimethylamine. Various industrial metal catalysts were evaluated, resulting in nearly quantitative mass balances for most catalysts. Identified intermediates, side and reaction products were placed into a corresponding reaction network, supported by kinetic evolution experiments. Cu‐ZrO2 was selected as most suitable catalyst combining high alcohol conversion with respectable aliphatic tertiary amine selectivity. Low pressure H2 was key for high catalyst activity and tertiary amine selectivity, mainly by hindering undesired reactant dimethylamine disproportionation and alcohol amidation. Besides dimethylamine model, diverse secondary amine reactants were tested with moderate to high tertiary amine yields. As most active catalytic site, highly dispersed Cu species in strong contact with ZrO2 is suggested. ToF‐SIMS, N2 O chemisorption, TGA and XPS of spent Cu‐ZrO2 revealed that imperfect amine product desorption and declining surface Cu lowered the catalytic activity upon catalyst reuse, while thermal reduction readily restored the initial activity and selectivity demonstratingAbstract: Upcoming biorefineries, such as lignin‐first provide renewable aromatics containing unique aliphatic alcohols. In this context, a Cu‐ZrO2 catalyzed hydrogen borrowing approach was established to yield tertiary amine from the lignin model monomer 3‐(3, 4‐dimethoxyphenyl)‐1‐propanol and the actual lignin‐derived monomers, (3‐(4‐hydroxyphenyl)‐1‐propanol and dihydroconiferyl alcohol), with dimethylamine. Various industrial metal catalysts were evaluated, resulting in nearly quantitative mass balances for most catalysts. Identified intermediates, side and reaction products were placed into a corresponding reaction network, supported by kinetic evolution experiments. Cu‐ZrO2 was selected as most suitable catalyst combining high alcohol conversion with respectable aliphatic tertiary amine selectivity. Low pressure H2 was key for high catalyst activity and tertiary amine selectivity, mainly by hindering undesired reactant dimethylamine disproportionation and alcohol amidation. Besides dimethylamine model, diverse secondary amine reactants were tested with moderate to high tertiary amine yields. As most active catalytic site, highly dispersed Cu species in strong contact with ZrO2 is suggested. ToF‐SIMS, N2 O chemisorption, TGA and XPS of spent Cu‐ZrO2 revealed that imperfect amine product desorption and declining surface Cu lowered the catalytic activity upon catalyst reuse, while thermal reduction readily restored the initial activity and selectivity demonstrating catalyst reuse. Abstract : Tertiary amines from lignin model monomers : A heterogeneous Cu‐ZrO2 catalyzed hydrogen borrowing strategy was developed to synthesize tertiary amines from lignin (model) monomers. Reusability of the easily recoverable catalyst was investigated by recycle experiments and in depth analysis of the spent catalyst (ToF‐SIMS, N2 O chemisorption, XPS and TGA). Thermal reduction proved to be an efficient catalyst regeneration strategy. … (more)
- Is Part Of:
- ChemSusChem. Volume 15:Issue 19(2022)
- Journal:
- ChemSusChem
- Issue:
- Volume 15:Issue 19(2022)
- Issue Display:
- Volume 15, Issue 19 (2022)
- Year:
- 2022
- Volume:
- 15
- Issue:
- 19
- Issue Sort Value:
- 2022-0015-0019-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-08-24
- Subjects:
- Amination -- Heterogeneous catalysis -- Hydrogen transfer -- Lignin -- tertiary amines
Green chemistry -- Periodicals
Sustainable engineering -- Periodicals
Chemistry -- Periodicals
Chemical engineering -- Periodicals
660 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%291864-564X ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cssc.202200868 ↗
- Languages:
- English
- ISSNs:
- 1864-5631
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3133.482500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 24049.xml