Selectivity in Tip-Induced Skeletal Editing via Heteroatom Substitution
Open Access
- 24 September 2026
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 148 (39) , 41755-41759
Abstract
Skeletal editing enables precise structural modifications of molecules at late stages of a synthetic sequence. We recently demonstrated skeletal editing on a single-molecule scale. Voltage pulses applied by the tip of a scanning probe microscope to an oxygen-containing seven-membered heterocycle led to both oxygen deletion and ring-contraction rearrangement reactions. An open question is whether selective skeletal editing of a heterocyclic core can be achieved by the choice of heteroatom. Here we show that tip-induced reactions of an analogous sulfur-containing seven-membered ring mainly result in sulfur deletion. Our results demonstrate that the combination of tip-induced chemistry and heteroatom selection in the molecular design is a powerful strategy for single-molecule skeletal editing, potentially enabling diverse structural transformations of heterocyclic frameworks.Keywords
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Funding Information
- European Regional Development Fund
- Xunta de Galicia (ED431G 2023/03)
- Spanish Agencia Estatal de Investigaci?n (PID2022-140845OB-C62)
- European Research Council Synergy grant MolDAM (951519)
- Swedish Research Council (2024-05250)
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