Datos del Documento


Por favor, use este identificador para citar o enlazar este documento: https://ria.asturias.es/RIA/handle/123456789/10866
Registro de Metadatos Completo
Campo Dublin Core Valor Idioma
dc.contributor.authorIlkaeva, Marina-
dc.contributor.authorKrivtsov, Igor-
dc.contributor.authorBartashevich, Ekaterina-
dc.contributor.authorKhainakov, Sergei-
dc.contributor.authorGarcía, Rubén-
dc.contributor.authorDíaz, Eva-
dc.contributor.authorOrdóñez, Salvador-
dc.date.accessioned2018-12-04T08:05:43Z-
dc.date.available2018-12-04T08:05:43Z-
dc.date.issued2017-08-11-
dc.identifier.citationGreen Chem., 2017, 19, 4299-4304eng
dc.identifier.urihttp://ria.asturias.es/RIA/handle/123456789/10866-
dc.description.abstractThe unprecedented ability of g-C3N4 to chemoselectively photo-oxidise the methyl group of 2-(4-methylphenoxy)ethanol instead of the easily oxidised oxyethanol fragment has been demonstrated. When g-C3N4 is treated with H2O2, its selectivity enhances due to the blocking of surface sites responsible for the adsorption and the subsequent oxidation of the oxyethanol substituent.eng
dc.language.isoengeng
dc.publisherRSCeng
dc.relation.ispartofGreen Chemistryeng
dc.relation.haspart19eng
dc.relation.isreferencedbySí, esta versión ha sido citadaeng
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.source4299;4304-
dc.subject.classificationPublicadoeng
dc.titleCarbon nitride assisted chemoselective C–H bond photo-oxidation of alkylphenolethoxylates in water mediumeng
dc.typearticleeng
Aparece en las colecciones: Open Access DRIVERset
Química

Archivos en este documento:
Fichero Tamaño Formato  
GreenChemistry.pdf566.36 kBAdobe PDFVer/Abrir
Mostrar el registro Básico


Ver estadísticas del documento


Este documento está sujeto a una licencia Creative Commons: Licencia Creative Commons Creative Commons