ArticleNature communications2026
On-surface synthesis platform for highly branched oligomers based on sequential C-C coupling and C-H activation of carbenes.
Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- Hydrogen-Bond Bifurcation as the Key Mechanism of Pyridine Surface Diffusion on MCM-41.ACS omega · 2026Article
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9 authors.
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Abstract
On-surface synthesis is an emerging field for fabricating low-dimensional nanostructures. While carbenes are versatile reactive intermediates in solution-phase organic synthesis, they have rarely been explored in on-surface synthesis. Here, we demonstrate the versatility of carbenes in synthesizing highly branched zero-dimensional oligomers with distinct structures on a metal surface by combining bond-resolved scanning tunneling microscopy imaging, manipulation, X-ray photoelectron spectroscopy, surface infrared spectroscopy, and ab initio theoretical modeling. We synthesize highly symmetric branched oligomers through the C-C coupling of two carbene molecules to form a core of oligomers, followed by C-H activation of the core with up to four additional carbene molecules to create branches. Branched oligomers of lower symmetry are formed through cyclodehydrogenation of the highly symmetric oligomers. Our on-surface synthetic strategy based on C-H activation of carbene building blocks provides a platform for the design and synthesis of highly branched zero-dimensional oligomers with distinct structures.
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