Green Synthesis of Copper Nanoparticles utilising the Maillard Reaction

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

Abstract

A new approach for the fabrication copper nanoparticles by a wet chemical reduction method is reported. The natural resources arginine as amino compound and several monosaccharides (xylose, ribose, galactose and glucose) react characteristically performing an Amadori rearrangement followed by a Maillard type reaction. This reaction carried out in an aqueous solution ensures an environmentally friendly way of reducing copper(II) ions leading to the formation of the desired nanoparticles. By changing the concentration of the amino acid, simultaneously acting as a complexing agent, it is possible to tune the size of the resulting nano particles to a certain degree down to 3 nm. This nontoxic and facile preparation route with quantitative yield opens a wide field of applications ranging from electronics to medical approaches.

Details

Original languageEnglish
Article numbere202404314
Number of pages6
JournalChemistry - A European Journal
Volume31
Issue number18
Publication statusPublished - 25 Mar 2025
Peer-reviewedYes

External IDs

unpaywall 10.1002/chem.202404314
PubMed 39912751

Keywords

Keywords

  • Amadori rearrangement, arginine, chemical reduction, copper, nanoparticles