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The influence of L ligands on the {RuNO}6/7 bonding situation in cis-[Ru(NO)(NO2)L1-4]q complexes: A theoretical insight

dc.contributor.authorAndriani K.F.
dc.contributor.authorCaramori G.F.
dc.contributor.authorMuñoz-Castro A.
dc.contributor.authorDoro F.G.
dc.date.accessioned2020-09-02T22:12:25Z
dc.date.available2020-09-02T22:12:25Z
dc.date.issued2015
dc.identifier10.1039/c5ra10888h
dc.identifier.citation5, 85, 69057-69066
dc.identifier.issn20462069
dc.identifier.urihttps://hdl.handle.net/20.500.12728/3604
dc.descriptionIt is regularly claimed that equatorial and axial ligands have a crucial role on the release of nitric oxide in ruthenium nitrosyl complexes. The reactivity of NO is dependent not only on the nature of the coordinated ligands but also on the bonding linkage isomerism that it can be involved. In this work, the interplay between the π-acceptor character of different L ligands and its effect on the Ru-NO bonding situation in {RuNO}6 and {RuNO}7 cores of cis-[Ru(NO)(NO2)L1-4]q complexes, where L = ammonia, 2,2′-bipyridine, 1,10′-phenanthroline and 1,4,8,11-tetraazacyclotetradecane ligands, is presented. The Ru-NO bonding situation is studied by the energy decomposition analysis of Su and Li, QTAIM and NBO methods. The nitrosyl-isonitrosyl isomerism is also investigated. Results show that complexes containing strong π-acceptor ligands (2,2′-bipyridine and 1,10′-phenanthroline) have their Ru-NO and Ru-ON interactions stabilized prior the NO reduction, while complexes containing weak π-acceptor ligands (ammonia and 1,4,8,11-tetraazacyclotetradecane) stabilize those interactions after reduction. © The Royal Society of Chemistry 2015.
dc.language.isoen
dc.publisherRoyal Society of Chemistry
dc.titleThe influence of L ligands on the {RuNO}6/7 bonding situation in cis-[Ru(NO)(NO2)L1-4]q complexes: A theoretical insight
dc.typeArticle


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