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Metallaaromatic biaryl atropisomers

dc.contributor.authorTalavera Nevado, María 
dc.contributor.authorPeña Gallego, Maria De Los Angeles 
dc.contributor.authorAlonso Gómez, José Lorenzo 
dc.contributor.authorBolaño García, Sandra 
dc.date.accessioned2024-09-16T10:25:04Z
dc.date.available2024-09-16T10:25:04Z
dc.date.issued2018
dc.identifier.citationChemical Communications, 54(78): 10974-10976 (2018)spa
dc.identifier.issn13597345
dc.identifier.issn1364548X
dc.identifier.urihttp://hdl.handle.net/11093/7429
dc.description.abstractSynthesis of stable irida-binaphthyl and -phenanthryl complexes, the first examples of metallaaromatic biaryl atropisomers, has been achieved. The combination of experimental and theoretical studies revealed that the nature of these systems is comparable to that of well-known 1,1′-binaphthalene both in terms of aromaticity and atropisomerism.en
dc.language.isoengspa
dc.publisherChemical Communicationsspa
dc.rightsCopyright © 2018 Royal Society of Chemistry
dc.titleMetallaaromatic biaryl atropisomersen
dc.typearticlespa
dc.rights.accessRightsopenAccessspa
dc.identifier.doi10.1039/C8CC06443A
dc.identifier.editorhttps://xlink.rsc.org/?DOI=C8CC06443Aspa
dc.publisher.departamentoQuímica inorgánicaspa
dc.publisher.departamentoQuímica Físicaspa
dc.publisher.grupoinvestigacionNovos Materiaisspa
dc.publisher.grupoinvestigacionQuímica Cuánticaspa
dc.subject.unesco2307 Química Físicaspa
dc.subject.unesco2303 Química Inorgánicaspa
dc.date.updated2024-08-22T10:51:45Z
dc.computerCitationpub_title=Chemical Communications|volume=54|journal_number=78|start_pag=10974|end_pag=10976spa


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