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Catalyst chirality switched with a flash of light

Molecular motor and chiral ligand combined to create photoresponsive catalyst

by Laura Howes
December 4, 2018

The chiral catalyst in two forms.
Ultraviolet light can switch the catalyst between two different forms.

Cells have a lot of control over enzymes. They can modify an enzyme to be more or less active, or to change the reaction that it catalyzes. But chemistry in the lab is different. “Normally when we design a ligand or catalyst we design it to do one specific transformation,” explains Ben Feringa of the University of Groningen, who won the 2016 Nobel Prize in Chemistry. “What we wanted to do is make an adaptive catalyst.”

To do that, Feringa’s group has combined a molecular motor with an existing asymmetric catalyst. The result is a catalyst that can switch its chirality, and as a result the stereochemistry of its products, with a flash of light (J. Am. Chem. Soc.2018, DOI: 10.1021/jacs.8b10816).

The switchable catalyst features what is known as axial chirality. This type of chirality is often used in asymmetric catalysis and results from the nonplanar arrangement of groups around an axis. Feringa’s molecule contains a biphenol group with axial chirality and a rigid core that rotates when hit with ultraviolet light. Because of the tight conformational coupling of these two elements, switching the helicity around the axis also changes the chirality of the biphenol. The biphenol coordinates with a zinc ion to form the active catalyst.

As a proof of principle, the chemists tested the catalyst in an organometallic 1,2-addition reaction to produce different stereoisomers depending on which form of the catalyst was used.

The catalyst is “a real achievement in the dynamic coupling of several types of convoluted chiralities,” says Nicolas Giuseppone, an organic chemist at the University of Strasbourg.

“It nicely demonstrates that switchable chiral catalysts can be obtained by the designed integration of functional units with well-defined stereochemical properties,” adds Alberto Credi of the University of Bologna. “Such a modular approach could in principle be applied to a wealth of biaryl structures,” he adds, suggesting this could lead to various chiral switches that could control different processes.

Feringa agrees. The dream, he says, is adaptive systems that could be switched from one reaction to another using an external signal. But, he admits, “I don’t know where the most useful applications will be.”


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