Document Detail


A Combined Experimental and DFT/TD-DFT Investigation of Structural, Electronic, and Cation-Induced Switching of Photophysical Properties of Bimetallic Ru(II) and Os(II) Complexes Derived from Imidazole-4,5-Dicarboxylic Acid and 2,2'-Bipyridine.
MedLine Citation:
PMID:  23738608     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Experimental results coupled with computational studies were utilized to investigate the structural and electronic properties of mixed-ligand bimetallic ruthenium(II) and osmium(II) complexes of composition [(bpy)2M(Imdc)M(bpy)2](+) [M = Ru(II) (1) and M = Os(II) (2)], where H3Imdc = imidazole-4,5-dicarboxylic acid and bpy = 2,2'-bipyridine. The X-ray crystal structures of both the bimetallic complexes were determined which showed that compound 1 crystallizes in monoclinic form with space group P2(1)/c, while 2 is obtained in orthorhombic form with the space group Pca2(1). The optimized geometrical parameters for the complexes computed both in the gas phase and in solution are reported and compared with the single-crystal X-ray data. The absorption spectra, redox behaviors, and luminescence properties of the complexes were thoroughly investigated. The complexes display very intense, ligand-centered absorption bands in the UV and moderately intense MLCT bands in the visible regions. While the Ru(II) complex displays moderately strong luminescence, the corresponding Os(II) complex does not luminesce at room temperature. Both the bimetallic complexes show two successive one-electron reversible metal-centered oxidations. The effect of alkali, alkaline earth, and transition metal cations on the absorption and emission spectral behavior of the complexes has also been studied in detail. As compared to the luminescence intensities and the quantum yields of the free complexes, those of the complexes were enhanced substantially in the presence of selective cations showing cation-induced molecular switching behaviors. Density functional theory (DFT) and time-dependent DFT (TD-DFT) studies provide insight into the nature of the ground and excited states with resulting detailed assignments of the orbitals involved in absorption and emission transitions. In particular, the blue-shifts of the absorption and emission bands in the presence of cations are also reproduced by our calculations.
Authors:
Shyamal Das; Srikanta Karmakar; Debasish Saha; Sujoy Baitalik
Related Documents :
22412458 - Bis[n-(2-hy-droxy-eth-yl)-n-methyl-dithio-carbamato-κs][2,4,6-tris-(pyridin-2-yl)-1,3,5...
23361638 - Solvatochromic behavior of chiral mesoporous metal-organic frameworks and their applica...
12456968 - The structure of orange hgi2. i. polytypic layer structure.
15299738 - X-ray structure of a new crystal form of pike 4.10 beta parvalbumin.
23219858 - Dinitrosyl iron complexes with glutathione as no and no(+) donors.
12027708 - Effect of geminal substitution on the strain energy of dioxiranes. origin of the low ri...
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2013-6-5
Journal Detail:
Title:  Inorganic chemistry     Volume:  -     ISSN:  1520-510X     ISO Abbreviation:  Inorg Chem     Publication Date:  2013 Jun 
Date Detail:
Created Date:  2013-6-6     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  0366543     Medline TA:  Inorg Chem     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Department of Chemistry, Inorganic Chemistry Section, Jadavpur University , Kolkata - 700 032, India.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Composition characterization and clinical efficacy study of a salmon egg extract.
Next Document:  Prevalence of obesity and associated cardiovascular risk: the DARIOS study.