Carbene-activated stannylenes to access selective C(sp3)–H bond scission at the steric limit
Jennifer Klaucke,
Navutheya Sinthathurai,
Christopher Golz,
Oliver P. E. Townrow () and
Malte Fischer ()
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Jennifer Klaucke: Georg-August-Universität Göttingen
Navutheya Sinthathurai: Georg-August-Universität Göttingen
Christopher Golz: Georg-August-Universität Göttingen
Oliver P. E. Townrow: Karlsruher Institut für Technologie
Malte Fischer: Georg-August-Universität Göttingen
Nature Communications, 2025, vol. 16, issue 1, 1-9
Abstract:
Abstract The ubiquity of N-heterocyclic carbenes (NHCs) in diverse areas of chemical research typically arises from their potent stabilising capabilities and role as innocent spectators to stabilise otherwise non-bottleable compounds and complexes. This has, until now, been particularly true for NHC-stabilised stannylenes, with no exceptions reported thus far. Herein, we demonstrate that the combination of heteroleptic terphenyl-/amido-based stannylenes and tetra-alkyl substituted NHCs renders the corresponding NHC-ligated stannylenes highly reactive, yet isolable. In solution, this induces sterically controlled inter- and intramolecular C(sp3)–H bond scissions, resulting in the selective formation of stannylene metallocycles that depend on both the NHC source and the meta-terphenyl ligand coordinated to tin.
Date: 2025
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-57907-2
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DOI: 10.1038/s41467-025-57907-2
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