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dc.contributorWichita State University. Department of Chemistryen_US
dc.contributor.authorWang, Youxiangen_US
dc.contributor.authorPerez, Willie J.en_US
dc.contributor.authorZheng, Greg Y.en_US
dc.contributor.authorRillema, D. Paulen_US
dc.contributor.authorHuber, Connie L.en_US
dc.date.accessioned2012-02-06T17:15:42Z
dc.date.available2012-02-06T17:15:42Z
dc.date.issued1998-05-04en_US
dc.identifier11670379en_US
dc.identifier0366543en_US
dc.identifieric970534+en_US
dc.identifier.citationInorganic chemistry. 1998 May 4; 37(9): 2227-2234.en_US
dc.identifier.issn1520-510Xen_US
dc.identifier.issn0020-1669en_US
dc.identifier.urihttp://hdl.handle.net/10057/4250
dc.descriptionFull text of this article is not available in SOAR.en_US
dc.description.abstractA series of bimetallic complexes of ruthenium(II) bridged by heterocyclic ligands formed by the condensation of 4,5-diazafluoren-9-one with various diamines, hydrazine, 1,4-phenylenediamine, benzidine, and 4,4'-methylenedianiline, results in metal centers separated by various distances. The complexes give rise to metal-to-ligand charge-transfer absorptions in the 450 nm region of the visible spectrum and intraligand pi --> pi transitions in the 300 nm region of the ultraviolet spectrum. The ruthenium(II) centers are oxidized in two closely spaced one-electron processes at potentials more positive than that for Ru(bpy)(3)(2+). The bridging ligands are reduced by two closely spaced one-electron processes at more positive potentials than that for reduction of the coordinated bipyridine ligands ( approximately -1.30 V), although the diazafluorene=N-N=diazafluorene bridging ligand is reduced reversibly in two single-electron steps at E(1/2) values of -0.29 and -0.52 V. After purification by eluting the "pure" complexes over a silica gel column with various concentrations of 0.10 M NH(4)PF(6) in methanol, emission occurs only in a glassy matrix at 77 K and at low temperatures in solution. The emission lifetimes at 77 K in a 4:1 ethanol:methanol glass are 5 +/- 1 &mgr;s. A variable-temperature emission lifetime study reveals the presence of a low-lying state with DeltaE = approximately 1500 cm(-)(1), and extrapolation to room temperature indicates the emission lifetimes are in the subnanosecond range.en_US
dc.format.extent2227-2234en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.ispartofseriesInorganic chemistryen_US
dc.relation.ispartofseriesInorg Chemen_US
dc.sourceNLMen_US
dc.titlePreparation, Purification, and Characterization of Binuclear Ruthenium(II) Complexes: Bridging Ligands Based on Diazafluorenesen_US
dc.typeArticleen_US
dc.description.versionpeer revieweden_US
dc.rights.holderCopyright © 1998 American Chemical Societyen_US


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