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Authordc.contributor.authorMendizábal Emaldía, Fernando 
Authordc.contributor.authorOlea Azar, Claudio es_CL
Admission datedc.date.accessioned2010-06-08T16:16:29Z
Available datedc.date.available2010-06-08T16:16:29Z
Publication datedc.date.issued2002-03-15
Cita de ítemdc.identifier.citationINTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY 87 (2): 89-100en_US
Identifierdc.identifier.issn0020-7608
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/120978
Abstractdc.description.abstractThe electronic structures of complexes and one-dimensional metallomacrocycles with cyanide as bridged ligand, such as [MacM(CN)(2)](-) and [MacM(CN)](n) [Mac = phthalocyanine, tetrabenzoporphyrine; M = Co(III), Rh(III)] have been investigated using density functional theory. The results of this study show that the intrinsic semiconductivity properties depend on the frontier bands. The valence band is composed by the pi-macrocycle orbital. The conduction band for the cobalt polymers is a mixture of orbitals between this metal and the cyanide ligand along of the stacking direction. However, in the rhodium polymers such a band is exclusively composed of the pi* system of the macrocycles.en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherJOHN WILEY & SONS INCen_US
Keywordsdc.subjectMetallomacrocycles complexes and polymersen_US
Títulodc.titleMetallomacrocycle (MacM) complex with cyanide as bridged ligand: Electronic structures of [MacMCN](n)en_US
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorcrb


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