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Micellar catalysis of the Suzuki Miyaura reaction using biogenic Pd nanoparticles from<i>Desulfovibrio alaskensis</i>

Yuta Era, Jonathan A. Dennis, Stephen Wallace, Louise Horsfall

2021Green Chemistry18 citationsDOIOpen Access PDF

Abstract

G20 catalyse the ligand-free Suzuki Miyaura reaction of abiotic substrates. The reaction is highly efficient (>99% yield, 0.5 mol% Pd), occurs under mild conditions (37 °C, aqueous media) and can be accelerated within biocompatible micelles at the cell membrane to yield products containing challenging biaryl bonds. This work highlights how native metabolic processes in anaerobic bacteria can be combined with green chemical technologies to produce highly efficient catalytic reactions for use in sustainable organic synthesis.

Topics & Concepts

ChemistryCatalysisPalladiumYield (engineering)Metal ions in aqueous solutionMicelleLigand (biochemistry)DesulfovibrioNanoparticleCombinatorial chemistryMetalAqueous solutionOrganic chemistrySulfateNanotechnologyMaterials scienceBiochemistryReceptorMetallurgyAdvanced Nanomaterials in CatalysisNanocluster Synthesis and ApplicationsNanoparticles: synthesis and applications
Micellar catalysis of the Suzuki Miyaura reaction using biogenic Pd nanoparticles from<i>Desulfovibrio alaskensis</i> | Litcius