A post-synthetic modification strategy for the synthesis of pyrene-fused azaacene covalent organic frameworks
Post-synthetic modification strategy is presented to extend the π-system of covalent organic framework (COF) backbone giving access to boronic ester based pyrene-fused azaacene COFs. Optimized catalyst-free reaction conditions yield COFs post-synthetically modified with up to 33% conversion and corr...
| Autores: | , , , , , , , , , , |
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| Tipo de documento: | artigo |
| Estado: | Versión aceptada para publicación |
| Data de publicação: | 2022 |
| País: | España |
| Recursos: | Consejo Superior de Investigaciones Científicas (CSIC) |
| Repositório: | DIGITAL.CSIC. Repositorio Institucional del CSIC |
| OAI Identifier: | oai:digital.csic.es:10261/279613 |
| Acesso em linha: | http://hdl.handle.net/10261/279613 https://api.elsevier.com/content/abstract/scopus_id/85137302055 |
| Access Level: | Acceso aberto |
| Palavra-chave: | Post-synthetic modification Azaacene Covalent organic frameworks Optical properties |
| Resumo: | Post-synthetic modification strategy is presented to extend the π-system of covalent organic framework (COF) backbone giving access to boronic ester based pyrene-fused azaacene COFs. Optimized catalyst-free reaction conditions yield COFs post-synthetically modified with up to 33% conversion and corresponding intriguing optical properties. The presented chemistry is expected to find application in post-synthetic tailoring of the optical properties of COFs. |
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