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Zapping Diels-Alder reactions

Electric field spurs reagents to join up in a non-redox transformation

by Bethany Halford
March 2, 2016 | APPEARED IN VOLUME 94, ISSUE 10

An electric field can trigger a Diels-Alder reaction.
An electric field can trigger a Diels-Alder reaction.

In a discovery that might come as a shock—or, at the very least, an electric shock—chemists have found that a properly oriented external electric field can nudge two reagents to hook up with one another in a Diels-Alder reaction. The fundamental discovery expands chemists’ knowledge of how electricity can drive synthesis and catalysis (Nature 2016, DOI: 10.1038/nature16989).

Chemists have long used electricity to trigger redox reactions. And theorists have suggested that electric fields could spur on non-redox transformations, but until now, no one had shown this was possible with a bimolecular system. “What is particularly striking is that we chose a really simple nonpolar carbon-carbon-bond-forming reaction—a Diels-Alder reaction—for which there are no formal zwitterionic intermediates involved,” says Michelle L. Coote, a professor at Australian National University who coauthored the study. “So we think these electric field effects could be very general.”

Coote and her collaborators, University of Wollongong’s Simone Ciampi and University of Barcelona’s Nadim Darwish and Ismael Diez-Perez, were inspired by the work of Hebrew University of Jerusalem theorist Sason Shaik, who suggested that an oriented electric field might accelerate Diels-Alder reactions. To prove this experimentally, Coote and her colleagues tethered a dienophile to a gold surface and a diene to the tip of a scanning-tunneling microscope.

They brought the molecules close to one another and applied an electric field. Upping the power of the electric field led to an increase in the reaction rate. What’s more, the field’s polarity mattered: The reaction rate only got a boost when the electric field favored electron flow from the dienophile to the diene.

Shaik tells C&EN he was delighted to see his theory, which had been described as “daydreaming,” proven experimentally. Although the current method can’t synthesize products on a practical scale, he thinks the discovery has the potential to change how chemists make molecules. “I definitely see a future where instead of mixing chemicals in a flask and heating, you will zap molecules with an electric field,” he says.



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Douglas Armstrong, Professor of Chemistry (March 10, 2016 4:01 PM)
A couple of my research students and I have had some successes with Diels-Alder reactions, but, admittedly we have struggled with incomplete (and sometimes failing) DA reactions in the last couple years. Although I have a couple ideas how this might be resolved (including possibly trying to prevent retro-Diels-Alder, and/or proper use of the "IED" principle), I wonder if this zapping discovery can possibly be developed enough, so as to be able to actually synthesize compounds, even though Dr. Shaik pointed out that it has not (yet) been developed to that point. I would consider collaborating with him (and/or anyone else) toward possibilities of developing this to that point. I gave a poster presentation on our Diels-Alder work at the 2015 Heterocyclic Gordon Research Conference, and will be putting that onto "Digital Commons" very soon, for other chemists to see what we have done. I would like to hear from him and/or any other chemist who might consider collaborating, either before or after seeing our poster on Digiital Commons.

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