Johannes G. H. Hermens

ORCID: 0000-0003-4762-1595
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About
Contact & Profiles
Research Areas
  • Catalysis for Biomass Conversion
  • Chemistry and Chemical Engineering
  • Innovative Microfluidic and Catalytic Techniques Innovation
  • Chemical Synthesis and Reactions
  • Carbon dioxide utilization in catalysis
  • Oxidative Organic Chemistry Reactions
  • Radical Photochemical Reactions
  • Organic Chemistry Cycloaddition Reactions
  • Catalytic Cross-Coupling Reactions
  • Catalytic C–H Functionalization Methods
  • Photochromic and Fluorescence Chemistry
  • Synthesis of Indole Derivatives
  • Product Development and Customization
  • Mesoporous Materials and Catalysis
  • X-ray Diffraction in Crystallography
  • Synthetic Organic Chemistry Methods
  • Porphyrin and Phthalocyanine Chemistry
  • Catalytic Processes in Materials Science
  • Crystallization and Solubility Studies

University of Groningen
2020-2024

We describe the optimization and scale-up of two consecutive reaction steps in synthesis bio-derived alkoxybutenolide monomers that have been reported as potential replacements for acrylate-based coatings ( Sci. Adv. 2020, 6, eabe0026). These are synthesized by (i) oxidation furfural with photogenerated singlet oxygen followed (ii) thermal condensation desired 5-hydroxyfuranone intermediate product an alcohol, a step which until now has involved lengthy batch reaction. The successfully...

10.1021/acs.oprd.3c00462 article EN cc-by Organic Process Research & Development 2024-05-09

Biomass-derived butenolides are presented as green alternatives for acrylates in coatings with tunable properties.

10.1126/sciadv.abe0026 article EN cc-by-nc Science Advances 2020-12-16

Petrochemical based polymers, paints and coatings are cornerstones of modern industry but our future sustainable society demands greener processes renewable feedstock materials. A challenge is to access platform monomers from biomass resources while integrating the principles green chemistry in their chemical synthesis. We present a synthesis route starting biomass-derived furfural towards commonly used maleic anhydride acrylic acid, implementing environmentally benign photooxygenation,...

10.1002/anie.202112618 article EN Angewandte Chemie International Edition 2021-11-16

A complete biobased process towards polymers and coatings using starting materials derived from renewable resources implementing sustainable synthetic steps.

10.1039/d2gc03657f article EN cc-by-nc Green Chemistry 2022-01-01

Butenolides are a class of 5-membered lactones that hold great potential as bio-based monomers to replace oil-derived acrylates, which they cyclic analogues. Despite this structural resemblance, the reactivity unsaturated ester moiety electron-poor butenolides leans toward maleic anhydride, another essential monomer does not homopolymerize but copolymerizes in highly alternating fashion with polarized electron-rich comonomers. By studying 5-methoxy and 5-acyloxy through combination kinetics...

10.1021/jacs.3c04314 article EN cc-by Journal of the American Chemical Society 2023-07-27

An easily-built, user-friendly modular photoreactor enables optimization and upscaling of flow photooxidation.

10.1039/d2re00310d article EN cc-by-nc Reaction Chemistry & Engineering 2022-01-01

Abstract Petrochemical based polymers, paints and coatings are cornerstones of modern industry but our future sustainable society demands greener processes renewable feedstock materials. A challenge is to access platform monomers from biomass resources while integrating the principles green chemistry in their chemical synthesis. We present a synthesis route starting biomass‐derived furfural towards commonly used maleic anhydride acrylic acid, implementing environmentally benign...

10.1002/ange.202112618 article EN Angewandte Chemie 2021-11-16

We describe the optimization and scale-up of two consecutive reaction steps in synthesis bio-derived alkoxybutenolide monomers that have been reported as potential replacements for acrylate-based coatings (Sci. Adv., 2020, 6, eabe0026). These are synthesized by (i) oxidation furfural with photo-generated singlet oxygen followed (ii) thermal condensation desired 5-hydroxyfuranone intermediate product an alcohol, a step which until now has involved lengthy batch reaction. The successfully...

10.26434/chemrxiv-2023-fcf2w preprint EN cc-by-nc-nd 2023-11-08

We describe the optimization and scale-up of two consecutive reaction steps in synthesis bio-derived alkoxybutenolide monomers that have been reported as potential replacements for acrylate-based coatings (Sci. Adv., 2020, 6, eabe0026). These are synthesized by (i) oxidation furfural with photo-generated singlet oxygen followed (ii) thermal condensation desired 5-hydroxyfuranone intermediate product an alcohol, a step which until now has involved lengthy batch reaction. The successfully...

10.26434/chemrxiv-2023-fcf2w-v2 preprint EN cc-by-nc-nd 2023-11-14

Due to the highly selective nature of singlet oxygen as an oxidant, it has received considerable interest in various areas (organic) chemistry. Two green light activated hydrazone-based boron difluoride triplet photosensitizers possessing high quantum yields for 1O2 formation are reported. These photostable complexes promising applications synthesis and catalysis.

10.1039/d2cc05336e article EN cc-by-nc Chemical Communications 2022-12-20
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