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dc.rights.licensehttp://creativecommons.org/licenses/by-nc-sa/3.0/ve/
dc.contributor.authorSuárez B., Trino
dc.contributor.authorFontal, Bernardo
dc.contributor.authorParra, María F.
dc.contributor.authorReyes, Marisela del C.
dc.contributor.authorBellandi, Fernando
dc.contributor.authorDíaz, Juan C.
dc.contributor.authorCancines, Pedro I.
dc.contributor.authorFonseca V., Yuraima J.
dc.date.accessioned2011-08-12T01:59:10Z
dc.date.available2011-08-12T01:59:10Z
dc.date.issued2010-01-12
dc.identifier.urihttp://www.saber.ula.ve/handle/123456789/33633
dc.descriptionArtículo Publicado en Springer Science+Business Media B.V. 2010es_VE
dc.description.abstractMer-[Mo(CO)3(p-C5H4N-CN)3] was prepared by UV-irradiation of a THF solution of Mo(CO)6 and paracyanopyridine under heating. The complex was characterized by FT-IR, MS, 1H and 13C NMR and showed catalytic activity for olefin hydroformylation (1-hexene, cyclohexene and 2,3-dimethyl-2-butene as model olefins; 600 psi synthesis gas (pCO/pH2 = 1); 100 C; 24 h; toluene). An examination of the complex catalyzed hydroformylation of a real naphtha cut (El Palito refinery, Venezuela), under the same conditions, also showed activity in the conversion to oxygenated products.es_VE
dc.language.isoenes_VE
dc.publisherSpringer Science+Business Media B.V. 2010es_VE
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleSynthesis, characterization and olefin hydroformylation reactions of mer-[Mo(CO)3(p-C5H4N-CN)3]es_VE
dc.typeinfo:eu-repo/semantics/article
dc.description.emailsuarez@ula.vees_VE
dc.description.emailfontal@ula.ve, bfontal@hotmail.comes_VE
dc.description.emailreyes@ula.vees_VE
dc.description.emailbellandi@ula.vees_VE
dc.description.emailcancines@ula.vees_VE
dc.description.emailfonsy@ula.vees_VE
dc.subject.facultadFacultad de Cienciases_VE
dc.subject.thematiccategoryQuímicaes_VE
dc.subject.tipoArtículoses_VE
dc.subject.unidadinvLaboratorio de Organometálicoses_VE
dc.type.mediaTextoes_VE


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