This article has been reviewed according to Science X's editorial process and policies. Editors have highlighted the following attributes while ensuring the content's credibility: Many useful reactions in chemistry come with a trade-off: the reactive reagents that make them effective can also present practical and safety challenges. Carbene chemistry is one such example.
For decades, chemists have relied on diazo compounds to generate reactive carbenes, even though diazoalkanes can be toxic, unstable and potentially explosive. Researchers at the Max-Planck-Institut für Kohlenforschung have now developed a safer approach to accessing metal carbenes. The study, published in Nature, shows that bench-stable thianthrenium salts can serve as practical and versatile precursors for carbene-transfer reactions.
Sulfonium salts, although safer, have not been useful as general carbene precursors. Sulfonium ylides are inherently nucleophilic, and carbene transfer from them to generate electrophilic metal carbenes is compromised by the Lewis basicity of the corresponding sulfides. The approach demonstrated by Tobias Ritter's group changes the picture.
The unusual electronic and steric properties of thianthrene make carbene transfer to the metal more favorable, overcoming a long-standing limitation in sulfonium-based carbene chemistry. The researchers demonstrated this metal-mediated reactivity through cyclopropanation, combining diverse carbene fragments with a broad range of alkenes, including challenging internal, unactivated alkenes. Deepak Behera says, "Sulfonium ylides have been used in cyclopropane chemistry for almost 60 years, but their reactivity was limited to Michael acceptors." Alkyl thianthrenium salts are readily prepared, bench-stable compounds that can be isolated and stored, which avoids safety concerns associated with diazoalkanes.
Thermal analysis showed no detectable exotherm for the salts tested, which supports a favorable safety profile. The researchers also demonstrated decagram-scale cyclopropanation using solvent-free ball milling. "The combination of bench-stable reagents and solvent-free ball milling makes the carbene chemistry particularly attractive from a practical and scalability perspective," says Sagnik Chatterjee.
The researchers also demonstrated σ-bond insertion and sigmatropic rearrangements, which extend the use of thianthrenium ylides beyond cyclopropanation. "Our aim was to establish a general approach to carbene-transfer chemistry that allows diverse carbene fragments to participate in different classes of reactions," says Ritter, director at the Max-Planck-Institut für Kohlenforschung. The study establishes thianthrenium salts as a general platform for carbene-transfer chemistry and opens the possibility of applying the same concept to an even wider range of carbene-mediated transformations in the future.
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