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dc.contributor.author | Melero-Gutierrez, Manuel | es_ES |
dc.contributor.author | Díaz, Urbano | es_ES |
dc.contributor.author | Llabrés i Xamena, Francesc Xavier | es_ES |
dc.date.accessioned | 2024-07-16T18:02:35Z | |
dc.date.available | 2024-07-16T18:02:35Z | |
dc.date.issued | 2024-04 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/206223 | |
dc.description.abstract | [EN] This study reports on a metal-free Covalent Triazine Framework (CTF) incorporating bithiophene structural units (TP-CTF) with a semicrystalline structure as an efficient heterogeneous photocatalyst under visible light irradiation. The physico-chemical properties and composition of this material was confirmed via different characterization solid-state techniques, such as XRD, TGA, CO2 adsorption and FT-IR, NMR and UV-Vis spectroscopies. The compound was synthesized through a solvothermal process and was explored as a heterogeneous photocatalyst for the oxidative coupling of amines to imines under visible light irradiation. TP-CTF demonstrated outstanding photocatalytic activity, with high conversion rates and selectivity. Importantly, the material exhibited exceptional stability and recyclability, making it a strong candidate for sustainable and efficient imine synthesis. The low bandgap of TP-CTF enabled the efficient absorption of visible light, which is a notable advantage for visible-light-driven photocatalysis. | es_ES |
dc.description.sponsorship | Financial support from the Spanish Ministry of Science and Innovation (PID2020-112590GBC21 and CEX2021-001230-S grants funded by MCIN/AEI/10.13039/501100011033) is gratefully acknowledged. This study forms part of the Advanced Materials Program and was supported by MICIN with funding from European Union NextGeneration (PRTR-C17.I1) and by the Generalitat Valenciana (MFA/2022/003). M. M. acknowledges financial support from FPI PhD fellowship PRE2018-084071. | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | MDPI AG | es_ES |
dc.relation.ispartof | Molecules | es_ES |
dc.rights | Reconocimiento (by) | es_ES |
dc.subject | Covalent triazine frameworks | es_ES |
dc.subject | Organic photocatalysis | es_ES |
dc.subject | Benzylamine coupling | es_ES |
dc.title | Thiophene-Based Covalent Triazine Frameworks as Visible-Light-Driven Heterogeneous Photocatalysts for the Oxidative Coupling of Amines | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.3390/molecules29071637 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-112590GB-C21/ES/MATERIALES HIBRIDOS DE BAJA DIMENSIONALIDAD CON MORFOLOGIA, ESTRUCTURACION Y REACTIVIDAD CONTROLABLE PARA LLEVAR A CABO PROCESOS CATALITICOS Y NANOTECNOLOGICOS / | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/GVA//MFA%2F2022%2F003/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//CEX2021-001230-S/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//PRTR-C17.I1/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//PRE2018-084071/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.description.bibliographicCitation | Melero-Gutierrez, M.; Díaz, U.; Llabrés I Xamena, FX. (2024). Thiophene-Based Covalent Triazine Frameworks as Visible-Light-Driven Heterogeneous Photocatalysts for the Oxidative Coupling of Amines. Molecules. 29(7). https://doi.org/10.3390/molecules29071637 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.3390/molecules29071637 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 29 | es_ES |
dc.description.issue | 7 | es_ES |
dc.identifier.eissn | 1420-3049 | es_ES |
dc.identifier.pmid | 38611916 | es_ES |
dc.identifier.pmcid | PMC11013671 | es_ES |
dc.relation.pasarela | S\521989 | es_ES |
dc.contributor.funder | Generalitat Valenciana | es_ES |
dc.contributor.funder | Agencia Estatal de Investigación | es_ES |
dc.contributor.funder | Ministerio de Ciencia e Innovación | es_ES |