This smart catalyst cracks a challenge that stumped chemists for decades
A clever digital search uncovered the key ingredient that turns stubborn molecules into powerful building blocks.
- Date:
- November 26, 2025
- Source:
- Hokkaido University
- Summary:
- Using a smart computational search, scientists discovered a catalyst ingredient that finally makes tough alkyl ketones behave the way chemists want. The reaction now runs cleanly and reliably, opening the door to faster and easier molecule-building.
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Ketones appear throughout organic molecules, which is why chemists are eager to create new reactions that take advantage of them when forming chemical bonds. One reaction that has remained especially difficult is the one-electron reduction of ketones needed to generate ketyl radicals. These radicals are highly useful intermediates in natural product synthesis and pharmaceutical research, but most available techniques are designed for aryl ketones rather than simpler alkyl ketones. Although alkyl ketones are far more common, they are also naturally harder to reduce than their aryl counterparts. With this challenge in mind, a team of organic and computational chemists at WPI-ICReDD at Hokkaido University has developed a catalytic strategy that finally enables the formation of alkyl ketyl radicals. The study appears in the Journal of the American Chemical Society and is available open access.
In earlier work, WPI-ICReDD scientists showed that a palladium catalyst paired with phosphine ligands could drive light-activated (reaction activated by shining light) transformations of aryl ketones, but the same system did not work for alkyl ketones. Their data indicated that alkyl ketyl radicals did form briefly. However, these radicals immediately returned an electron to the palladium center, a phenomenon known as back electron transfer (BET), before any useful reaction could proceed. As a result, the starting material remained unchanged.
Similar to traditional palladium-based catalysis, the behavior of photoexcited palladium catalysts is highly dependent on the phosphine ligand attached to the metal. The team suspected that choosing the correct ligand might unlock reactivity with alkyl ketones. The difficulty was scale: thousands of phosphine ligands exist, and experimentally screening them for an unfamiliar reaction would be slow, labor-intensive, and generate unnecessary chemical waste.
To overcome these limitations, the researchers turned to computational chemistry to narrow down the field of candidate ligands. They used the Virtual Ligand-Assisted Screening (VLAS) approach developed by Associate Professor Wataru Matsuoka and Professor Satoshi Maeda at WPI-ICReDD. Applying VLAS to 38 phosphine ligands, the method produced a heat map that predicted how well each ligand might promote the desired reactivity by analyzing electronic and steric properties.
Guided by these predictions, the team selected three ligands for laboratory testing and ultimately identified L4 as the most effective option -- tris(4-methoxyphenyl)phosphine (P(p-OMe-C6H4)3). This ligand successfully suppressed BET, allowing alkyl ketones to generate ketyl radicals and participate in high-yield transformations.
The resulting method provides chemists with an accessible way to work with alkyl ketyl radicals and demonstrates how VLAS can rapidly guide the development and optimization of new chemical reactions.
Story Source:
Materials provided by Hokkaido University. Note: Content may be edited for style and length.
Journal Reference:
- Kosaku Tanaka, Ren Yamada, Suvankar Debbarma, Wataru Kanna, Hiroki Hayashi, Wataru Matsuoka, Satoshi Maeda, Tsuyoshi Mita. Virtual Ligand-Assisted Screening for the Generation of Ketyl Radicals from Alkyl Ketones via Photoexcited Palladium Catalysis. Journal of the American Chemical Society, 2025; 147 (43): 39640 DOI: 10.1021/jacs.5c13115
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