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Authordc.contributor.authorMoya, Sergio A. 
Authordc.contributor.authorAraya, Juan Carlos es_CL
Authordc.contributor.authorGajardo, Juana es_CL
Authordc.contributor.authorGuerchais, Véronique es_CL
Authordc.contributor.authorBozec, Hubert Le es_CL
Authordc.contributor.authorToupet, Loïc es_CL
Authordc.contributor.authorAguirre Álvarez, Pedro es_CL
Admission datedc.date.accessioned2014-01-27T20:36:11Z
Available datedc.date.available2014-01-27T20:36:11Z
Publication datedc.date.issued2013
Cita de ítemdc.identifier.citationInorganic Chemistry Communications 27 (2013) 108–110en_US
Identifierdc.identifier.otherDOI: 10.1016/j.inoche.2012.09.028
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/121775
General notedc.descriptionArtículo de publicación ISIen_US
Abstractdc.description.abstractA series of novel complexes of the Ru(L)2(CO)2 L = 2-(3′ methoxyphenyl)-1,8-naphthyridine (complex 1), and type Ru(acac)2(L)(CO) with L = 2-(3′ methoxyphenyl)-1,8-naphthyridine (complex 2), 2-(2′- bromophenyl)-1,8-naphthyridine (complex 3) and 2-phenyl-1,8-naphthyridine (complex 4) was synthesized and characterized. We found that the complexes 2, 3, and 4 can be directly synthesized from Ru3(CO)12. The complex Ru(acac)2(L)(CO) L = 2-(3′ methoxyphenyl)-1,8-naphthyridine (2) was characterized by X-ray single crystal analysis which confirms the monodentate coordination mode of the 1,8-naphthyridine derivate and the cis arrangement of the acac ligands. Preliminary studies in transfer hydrogenation of acetophenone in the presence of 2-propanol show the good catalytic activity of complex 2 with 92% conversion.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherElsevieren_US
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Keywordsdc.subject1,8-Naphthyridineen_US
Títulodc.titleSynthesis and characterization of ruthenium (II) carbonyl complexes containing naphthyridine and acetylacetonate ligands and their catalytic activity in the hydrogen transfer reactionen_US
Document typedc.typeArtículo de revista


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile