Chemists create eco-friendly method to make chlorine-based materials for drugs and chemicals
“Our method uses sustainable, low-cost catalysts and operates at room temperature with gentle blue light”
Courtesy of Rice University
Led by Julian West, assistant professor of chemistry and a Cancer Prevention and Research Institute of Texas (CPRIT) Scholar, the research team developed a photocatalytic process that uses iron and sulfur catalysts activated by mild blue light to add chlorine atoms to organic molecules. This innovation eliminates the need for harsh chemicals or high temperatures typically required in chlorination, which can generate difficult-to-purify byproducts.
“Our method uses sustainable, low-cost catalysts and operates at room temperature with gentle blue light,” West said. “It provides a targeted, efficient way to chlorinate molecules without conventional approaches’ environmental and purification challenges.”
One advantage of the team’s method is its precise targeting of chlorine placement on molecules, a process called anti-Markovnikov hydrochlorination. This precision creates highly pure products by selectively attaching chlorine atoms to less-reactive parts of the starting molecules. With this approach, chemists can avoid extra purification steps that are often time-consuming and costly.
The researchers also unveiled a novel addition to this process: using heavy water to incorporate deuterium, a stable hydrogen isotope. This step could make certain drugs last longer in the body by increasing their stability, potentially enhancing their effectiveness.
“It’s exciting that this method could open new doors for modifying pharmaceuticals and natural products in ways that weren’t possible with older techniques,” West said.
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Kang-Jie Bian, David Nemoto, Ying Chen, Yen-Chu Lu, Shih-Chieh Kao, Xiao-Wei Chen, Angel A. Martí, Julian G. West; "Anti-Markovnikov hydro- and deuterochlorination of unsaturated hydrocarbons using iron photocatalysis"; Nature Synthesis, 2025-1-2
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