Reduction-Induced C─C Cleavage and Site-Specific Hydrogenation of a Highly Strained Bilayer Spironanographene

The chemical reduction of a bilayer spironanographene, spiro-NG (C137H120), with Na and K metals in the presence of [2.2.2]cryptand to yield [Na+(2.2.2-cryptand)](C137H121−) (1) and [K+(2.2.2-cryptand)](C137H121−) (2), respectively, is reported. X-ray crystallography reveals the formation of a new “...

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Detalles Bibliográficos
Autores: Lión Villar, Juan, Torchon, Herdya S., Zhu, Yikun, Wei, Zheing, Fernández García, Jesús Manuel, Fernández López, Israel, Petrukhina, Marina A., Martín León, Nazario
Tipo de recurso: artículo
Fecha de publicación:2025
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/123736
Acceso en línea:https://hdl.handle.net/20.500.14352/123736
Access Level:acceso abierto
Palabra clave:547
Química
2306 Química Orgánica
Descripción
Sumario:The chemical reduction of a bilayer spironanographene, spiro-NG (C137H120), with Na and K metals in the presence of [2.2.2]cryptand to yield [Na+(2.2.2-cryptand)](C137H121−) (1) and [K+(2.2.2-cryptand)](C137H121−) (2), respectively, is reported. X-ray crystallography reveals the formation of a new “naked” anion (spiro-NGH−), in which spirocyclic ring cleavage and subsequent hydrogenation have occurred. Density Functional Theory (DFT) calculations suggest that the generation of the radical anion of the parent nanographene (spiro-NG•−), upon electron acceptance from Na and K metals, induces the cleavage of the strained spirobifluorene core. The resulting spin density localizes on a particular carbon atom, previously attached to the spiranic sp3 carbon atom, facilitating a site-specific hydrogenation to afford (spiro-NGH−). The electrostatic potential map of this anion reveals electron density concentrated at the five-membered ring of the readily formed indenyl fragment, thus enhancing the aromaticity of the system. Furthermore, nuclear magnetic resonance (NMR) and UV–vis absorption spectroscopy experiments allowed to follow the in situ reduction and hydrogenation processes in detail.