Translating Photoredox Catalysis to Biological Environments

dc.contributor.advisorTomás Gamasa, María
dc.contributor.advisorMascareñas Cid, José Luis
dc.contributor.affiliationUniversidade de Santiago de Compostela. Escola de Doutoramento Internacional (EDIUS)
dc.contributor.authorFernández González, Xulián
dc.date.accessioned2026-04-20T07:50:15Z
dc.date.available2026-04-20T07:50:15Z
dc.date.issued2026
dc.description.abstractThis thesis explores the feasibility of performing photocatalytic radical processes in biological media, employing homogeneous and heterogeneous catalysis under a bioorthogonal context. First, we demostrated for the first time the photoredox activation of diazonium salts in biological and cellular environments, enabling radical transformations in cellulo. Subsequently, triazenes were introduce as stable precursors of diazonium salts, allowing the controlled generation of diazonium ion under aqueous and biocompatible conditions. As alternative radical precursors, we have explores the use of oximes for the generation of radical species under aqueoues conditions and within living cells. Finally, metal organic framewroks(MOF) were employeed as photocatalytic nanoreactors in aqueoues and biologically relevant environments.
dc.description.programaUniversidade de Santiago de Compostela. Programa de Doutoramento en Ciencia e Tecnoloxía Química
dc.identifier.urihttps://hdl.handle.net/10347/46801
dc.language.isoeng
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internationalen
dc.rights.accessRightsembargoed access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectBioorthogonal Chemistry
dc.subjectCu(I) catalyzed azide-alkyne cycloaddition (CuAAC)
dc.subjectstrain-promoted azide-alkyne cycloadditions (SPAAC)
dc.subjectvisible-light photocatalysis
dc.subjectAryldiazonium salts
dc.subject.classification230609 Radicales libres
dc.subject.classification230221 Biología molecular
dc.titleTranslating Photoredox Catalysis to Biological Environments
dc.typedoctoral thesis
dspace.entity.typePublication
relation.isAdvisorOfPublicationc50c2bff-089c-4f2b-865d-87d093c6db4a
relation.isAdvisorOfPublication5ae222c9-f626-432b-aac5-da78c06ed64f
relation.isAdvisorOfPublication.latestForDiscoveryc50c2bff-089c-4f2b-865d-87d093c6db4a

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