image: Image Credit: Yufei Zhang et al. ,Vicinal disubstitution of alkyl C–X synthons via alkene radical cation generation.Science0,eaef0766DOI:10.1126/science.aef0766.
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Credit: Yufei Zhang et al. ,Vicinal disubstitution of alkyl C–X synthons via alkene radical cation generation.Science0,eaef0766DOI:10.1126/science.aef0766.
Binghamton University chemists have discovered a new mechanism that could potentially lead to quicker outcomes in pharmaceutical research.
Carbon-halogen bonds are among the most common “handles” in organic chemistry, meaning that they’re added to molecules to enable or control a chemical reaction.
“They follow a simple rule: one handle, one substitution,” explained Binghamton University Associate Professor of Chemistry Jennifer Hirschi.
The halogen atom is removed and replaced with a new molecule, known as a functionality — a reaction taught in undergraduate courses. But in a recent study published in the journal Science, chemists outline a method that breaks this rule, using a single handle to add different groups to two neighboring carbon atoms.
The work was co-led by Hirschi and Patricia Musacchio, assistant professor of chemistry at the University at Buffalo, with the mechanistic studies carried out by Tamal Das, a postdoctoral researcher in the Hirschi lab. The research was funded by the National Institutes of Health.
Carbon atoms are integral to the molecules that make up many pharmaceuticals. In drug discovery research, these molecules are typically built one reaction at a time. Creating two chemical changes in a single step may shorten the route to a target, Hirschi explained.
Musacchio’s lab at Buffalo synthesized the new molecules, using off-the-shelf blue LED lights and a commercially available alcohol solvent familiar to undergraduate chemistry students. Meanwhile, Binghamton researchers used computational modeling to determine how the reaction happens, relying on density functional theory and ab initio molecular dynamics.
The blue light triggers a transfer of a hydrogen atom; this, along with an internal electronic rearrangement, converts a single carbon-halogen bond directly into a reactive intermediate known as an alkene radical cation. Typically, alkene radical cations only occur with strongly oxidizing catalysts, Hirschi explained.
The modeling revealed the driving force. The reaction occurs in a fluorinated alcohol solvent whose molecules form a network of hydrogen bonds around the departing halogen atom. That network stabilizes the halogen so effectively that the energy gained outweighs the energy required to break the carbon-halogen bond, allowing the intermediate to form under milder conditions.
Understanding this pathway served as a guide for the chemistry itself. Because the reactive intermediate presents two reactive sites side by side, a single handle can install two different groups on adjacent carbons in one operation. Guided by the mechanism, the researchers applied the approach to a range of everyday starting materials, including bromides, chlorides, fluorides, and even unprotected alcohols, forming new bonds to nitrogen, oxygen, and sulfur, and assembling small ring structures.
In a related variation, the halogen is shuttled to the neighboring carbon, where it becomes a fresh handle for further reactions. The mechanism now provides a framework for both the current method and future work, giving chemists a way to turn ordinary building blocks into more complex, drug-relevant structures in fewer steps, Hirschi said.
“The hope is to not only make drugs faster, but also make more complex drugs that can target more challenging medicinal goals,” Musacchio said.
About Binghamton University
Binghamton University offers students a broad, interdisciplinary education with an international perspective and one of the most vibrant research programs in the nation. The campus, recognized as an R1 institution for very high research activity by the Carnegie Classification of Institutions of Higher Education, recorded $87.3 million in research expenditures in 2024-25, its best year ever.
Journal
Science
DOI
10.1126/science.aef0766
Method of Research
Experimental study
Subject of Research
Not applicable
Article Title
Vicinal disubstitution of alkyl C–X synthons via alkene radical cation generation
Article Publication Date
9-Jul-2026
Media Contact
David Hermanovitch
Binghamton University
Cell: 607-222-3846
Journal
Science
DOI
10.1126/science.aef0766
Journal
Science
DOI
10.1126/science.aef0766
Method of Research
Experimental study
Subject of Research
Not applicable
Article Title
Vicinal disubstitution of alkyl C–X synthons via alkene radical cation generation
Article Publication Date
9-Jul-2026
Tags
/Physical sciences/Chemistry/Organic chemistry
Tags: alkene radical cation generationBlue LED lightcarbon-halogen bond activationchemical substitution mechanismsdrug discovery advancementinnovative synthesis methodslight-induced chemical reactionsnew chemical reactionorganic chemistrypharmaceutical researchradical cation chemistryVicinal disubstitution
