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An adamantane-based COF: stability, adsorption capability, and behaviour as a catalyst and support for Pd and Au for the hydrogenation of nitrostyrene

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An adamantane-based COF: stability, adsorption capability, and behaviour as a catalyst and support for Pd and Au for the hydrogenation of nitrostyrene

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Trandafir, MM.; Pop, L.; Hadade, ND.; Florea, M.; Neatu, F.; Teodorescu, CM.; Duraki, B.... (2016). An adamantane-based COF: stability, adsorption capability, and behaviour as a catalyst and support for Pd and Au for the hydrogenation of nitrostyrene. Catalysis Science & Technology. 6(23):8344-8354. https://doi.org/10.1039/c6cy01631f

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Título: An adamantane-based COF: stability, adsorption capability, and behaviour as a catalyst and support for Pd and Au for the hydrogenation of nitrostyrene
Autor: Trandafir, M. M. Pop, L. Hadade, N. D. Florea, M. Neatu, F. Teodorescu, C. M. Duraki, B. van Bokhoven, J. A. Grosu, I. Parvulescu, Vasile I. García Gómez, Hermenegildo
Entidad UPV: Universitat Politècnica de València. Departamento de Química - Departament de Química
Fecha difusión:
Resumen:
[EN] A bimodal (micro/mesoporous) COF was synthesized by coupling tetrakis-1,3,5,7-(4'-iodophenyl) adamantane with 4,4'-diethynylbiphenyl following a Sonogashira protocol. The COF preparation strategy led, however, to the ...[+]
Derechos de uso: Cerrado
Fuente:
Catalysis Science & Technology. (issn: 2044-4753 )
DOI: 10.1039/c6cy01631f
Editorial:
The Royal Society of Chemistry
Versión del editor: https://doi.org/10.1039/c6cy01631f
Código del Proyecto:
info:eu-repo/grantAgreement/ESF//POSDRU%2F187%2F1.5%2FS%2F155559/
info:eu-repo/grantAgreement/UEFISCDI//PCCA-II-166%2F2012/
info:eu-repo/grantAgreement/UEFISCDI//PCCA-II-56%2F2014/
info:eu-repo/grantAgreement/UEFISCDI//PN-II-ID-PCE-2011-3-0060/
info:eu-repo/grantAgreement/UEFISCDI//PN2-128%2F2011/
Agradecimientos:
This work was supported by a grant from the Romanian National Authority for Scientific Research, CNDI-UEFISCDI (project numbers PCCA-II-166/2012, PCCA-II-56/2014, and PN-II-ID-PCE-2011-3-0060). M. M. T. was supported by ...[+]
Tipo: Artículo

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