| Oct 12, 2023 |
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(Nanowerk News) New pharmaceuticals, cleaner fuels, biodegradable plastics: in order to meet society’s needs, chemists have to develop new synthesis methods to obtain new products that do not exist in their natural state. A research group at the University of Geneva (UNIGE), in collaboration with Cardiff University, has discovered how to use an external electric field to control and accelerate a chemical reaction, like a ‘switch’.
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Key Takeaways
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New research reveals an innovative method to control and accelerate chemical reactions using an external electric field.
The technique revolves around an electrochemical microfluidic reactor, where the progress of the chemical reaction directly correlates with the intensity of the applied electric field.
The electric field is produced between two electrodes, enhanced with carbon nanotubes, that induce electronic polarization in molecules, triggering the chemical transformation.
This revolutionary method holds potential for greener, simplified organic synthesis by reducing the need for complex, resource-intensive steps.
While there’s more to uncover regarding its full potential, this breakthrough can immensely impact organic chemistry, paving the way for environmentally-friendly production of drugs, fuels, and plastics.
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| The device takes the form of a small box in which the reaction medium circulates between two electrodes producing the electric field. (Image: Stefan Matile)
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The Research
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This work, published in Science Advances (“Electric-field-assisted anion-π catalysis on carbon nanotubes in electrochemical microfluidic devices”), could have a considerable impact on the development of new molecules, enabling not only more environmentally friendly synthesis, but also very simple external control of a chemical reaction.
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In chemistry, creating complex organic chemical compounds from simpler reagents is denoted ‘organic synthesis’. Through successive reactions, chemists assemble small molecules to ultimately form the desired products. Organic synthesis is crucial to the manufacture of drugs, polymers, agrochemicals, pigments and fragrances. These successive steps are extremely precise and delicate to control. To limit the required resources, the yield of each reaction step should be optimal. Achieving better control and simpler operation of these reactions remains a major research challenge.
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“Any molecular transformation results from electrons – negatively charged elementary particles – moving from one place in a molecule to another,” explains Stefan Matile, full professor in the Department of Organic Chemistry at the UNIGE’s Faculty of Science and part of the National Centre of Competence in Research (NCCR) Molecular Systems Engineering, who led the study. Electrons can be influenced by an external electric field. It is therefore theoretically possible to electrically control chemical reactions. Although simple in principle and promising in terms of impact, this approach has come up against several limitations, and its few implementations have performed poorly.
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A long-awaited breakthrough
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With their teams, Stefan Matile and his Cardiff University counterpart, professor Thomas Wirth, have succeeded in activating an organic chemical reaction with a simple electric field. To do this, they designed an electrochemical microfluidic reactor. Their results clearly show the dependence between the state of progress of the chemical reaction and the intensity of the applied electric field. This device enables a chemical reaction to be activated simply by flipping a switch.
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“This type of reactor takes the form of a small box in which the reaction mixture can circulate between two electrodes producing the electric field. The electrodes are 5 cm x 5 cm square plates placed as close together as possible. They are separated by a quarter-millimetre-thick sheet. This sheet contains the flow channel for circulating the molecules between the electrodes,” explains Ángeles Gutiérrez López, PhD student in Stefan Matile’s group and first author of the paper.
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The electrodes are coated with carbon nanotubes. As they flow through the reactor, the reactants interact weakly with the carbon nanotubes, exposing them to the electric field. This induces electronic polarization in the molecule, activating the chemical transformation.
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Towards greener activation of chemical reactions?
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To create the desired chemical bonds with a high yield, chemists usually implement complex, multi-step strategies involving numerous intermediates. These strategies require important resources and energy. The new electrical device proposed by Stefan Matile and Thomas Wirth could simplify these strategies and thus reduce the carbon impact of chemical syntheses.
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The device has the advantage of being easy to control. “Our ‘reactor’ is in some ways like the particle accelerator at CERN in Geneva, but instead of accelerating subatomic particles, it accelerates electrons during molecular transformations,” explains Stefan Matile. Fundamental advances are still needed to unlock the device’s full potential. However, this method could be applied to organic chemistry in the not-too-distant future, making the production of drugs, new fuels or new plastics greener and more controllable.
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