Expanding the BN-embedded PAH family: 4a-aza12a-borachrysene
Previously unknown 4a-aza-12a-borachrysene has been synthesized in only four steps. The reactions of this BN-embedded PAH with bromine and organolithium compounds proceed with complete regioselectivity, resulting in the formation of nine derivatives. One of these, a phenylalkynyl-substituted derivat...
| Autores: | , , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2020 |
| País: | España |
| Institución: | Universidad de Alcalá (UAH) |
| Repositorio: | e_Buah Biblioteca Digital Universidad de Alcalá |
| Idioma: | inglés |
| OAI Identifier: | oai:ebuah.uah.es:10017/43790 |
| Acceso en línea: | http://hdl.handle.net/10017/43790 https://dx.doi.org/10.1039/c9cc09998k |
| Access Level: | acceso abierto |
| Palabra clave: | BN-arene 4a-aza-12a-borachrysene Fluorescence Bromination Organolithium compound Química Chemistry |
| Sumario: | Previously unknown 4a-aza-12a-borachrysene has been synthesized in only four steps. The reactions of this BN-embedded PAH with bromine and organolithium compounds proceed with complete regioselectivity, resulting in the formation of nine derivatives. One of these, a phenylalkynyl-substituted derivative, exhibits a remarkably high fluorescence quantum yield (phiF = 0.68) |
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