B–N axis as a facilitating agent for the synthesis of 3D structures: the paradigmatic case of BN-[4.4.4]propellane
Flat aromatic compounds containing a boron–nitrogen (BN) fragment have gained significant attention in the field of organic optoelectronics. Unsurprisingly, therefore, an increasing number of synthetic methodology groups have devoted efforts and creativity to developing new strategies for accessing...
| Autores: | , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2025 |
| País: | España |
| Institución: | Universitat Ramon Llull (URL) |
| Repositorio: | DAU Arxiu Digital de la Universitat Ramon Llull |
| OAI Identifier: | oai:dau.url.edu:20.500.14342/5736 |
| Acceso en línea: | http://hdl.handle.net/20.500.14342/5736 https://doi.org/10.1039/D5SC05132K |
| Access Level: | acceso abierto |
| Palabra clave: | Aromatic compounds Compostos aromàtics Boron nitride Nitrur de bor 547 |
| Sumario: | Flat aromatic compounds containing a boron–nitrogen (BN) fragment have gained significant attention in the field of organic optoelectronics. Unsurprisingly, therefore, an increasing number of synthetic methodology groups have devoted efforts and creativity to developing new strategies for accessing diverse structures incorporating a B[double bond, length as m-dash]N unit, which is isosteric with the olefinic C[double bond, length as m-dash]C bond. In contrast, the potential of BN isosterism to expand the structural diversity of three-dimensional architectures based on sp3-hybridized atoms remains largely underexplored. In this study, we introduce a strategy to construct an alkane-type quaternary–quaternary Bsp3–Nsp3 molecular axis via double addition of a carbon-based nucleophile/electrophile pair to a readily accessible olefin-type B[double bond, length as m-dash]N moiety. The approach is showcased through the synthesis of a BN-[4.4.4]-propellane, in which the rapidly assembled tetrahydro-BN-naphthalene intermediate undergoes a polar double allylation of its B[double bond, length as m-dash]N bond. Despite the unfavorable trans preference in this addition step, efficient [4.4.4]-propellane formation was achieved through a tandem metathesis-based trans-to-cis isomerization and ring-closing reaction. The resulting BN-propellane exhibits a C3-symmetric helical arrangement in the solid state and shows fluxional behavior in the 1H NMR spectrum at room temperature due to a helicity flip, for which variable-temperature NMR measurements yielded an activation barrier (ΔG‡) of approximately 14.6 kcal mol−1. |
|---|