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Deactivation of Cu-3(BTC)(2) in the Synthesis of 2-Phenylquinoxaline

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Deactivation of Cu-3(BTC)(2) in the Synthesis of 2-Phenylquinoxaline

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Dhakshinamoorthy, A.; Alvaro Rodríguez, MM.; García Gómez, H. (2015). Deactivation of Cu-3(BTC)(2) in the Synthesis of 2-Phenylquinoxaline. Catalysis Letters. 145(8):1600-1605. https://doi.org/10.1007/s10562-015-1497-4

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Título: Deactivation of Cu-3(BTC)(2) in the Synthesis of 2-Phenylquinoxaline
Autor: Dhakshinamoorthy, Amarajothi Alvaro Rodríguez, Maria Mercedes García Gómez, Hermenegildo
Entidad UPV: Universitat Politècnica de València. Instituto Universitario Mixto de Tecnología Química - Institut Universitari Mixt de Tecnologia Química
Universitat Politècnica de València. Departamento de Química - Departament de Química
Fecha difusión:
Resumen:
[EN] Cu-3(BTC)(2) deactivates by deterioration of its crystal structure during the use of this metal organic framework as catalyst in the synthesis of 2-phenylquinoxaline from phenacylbromide and o-phenylenediamine at room ...[+]
Palabras clave: 2-Phenylquinoxaline , Cu-3(BTC)(2) , 2 as catalyst , Phenylquinoxaline , Heterogeneous catalysis , Metal organic frameworks , Heterocycle synthesis , Catalyst stability
Derechos de uso: Cerrado
Fuente:
Catalysis Letters. (issn: 1011-372X ) (eissn: 1572-879X )
DOI: 10.1007/s10562-015-1497-4
Editorial:
Springer Verlag
Versión del editor: http://dx.doi.org/10.1007/s10562-015-1497-4
Código del Proyecto:
info:eu-repo/grantAgreement/DST//SB%2FFT%2FCS-166%2F2013/
info:eu-repo/grantAgreement/EC/FP7/228862/EU/MOFs as Catalysts and Adsorbents: Discovery and Engineering of Materials for Industrial Applications/
info:eu-repo/grantAgreement/MINECO//CTQ2012-32315/ES/REDUCCION FOTOCATALITICA DEL DIOXIDO DE CARBONO/
info:eu-repo/grantAgreement/GVA//PROMETEO%2F2012%2F014/
Agradecimientos:
A.D.M. thanks University Grants Commission (UGC), New Delhi for the award of Assistant Professorship under its Faculty Recharge Programme. ADM also thanks Department of Science and Technology, India for the financial support ...[+]
Tipo: Artículo

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