Electrostatic catalysis of a click reaction in a microfluidic cell
Semih Sevim, Roger Sanchis‐Gual, Carlos Franco, Albert C. Aragonès, Nadim Darwish, Dong‐Hoon Kim, Rosaria Anna Picca, Bradley J. Nelson, Eliseo Ruíz, Salvador Pané, Ismael Díez‐Pérez, Josep Puigmartí‐Luis
Abstract
Electric fields have been highlighted as a smart reagent in nature's enzymatic machinery, as they can directly trigger or accelerate chemical processes with stereo- and regio-specificity. In enzymatic catalysis, controlled mass transport of chemical species is also key in facilitating the availability of reactants in the active reaction site. However, recent progress in developing a clean catalysis that profits from oriented electric fields is limited to theoretical and experimental studies at the single molecule level, where both the control over mass transport and scalability cannot be tested. Here, we quantify the electrostatic catalysis of a prototypical Huisgen cycloaddition in a large-area electrode surface and directly compare its performance to the conventional Cu(I) catalysis. Our custom-built microfluidic cell enhances reagent transport towards the electrified reactive interface. This continuous-flow microfluidic electrostatic reactor is an example of an electric-field driven platform where clean large-scale electrostatic catalytic processes can be efficiently implemented and regulated.