Luminescent dirhenium(I)-double-heterostranded helicate and mesocate

dc.contributor.author Shankar, Bhaskaran
dc.contributor.author Sahu, Saugata
dc.contributor.author Deibel, Naina
dc.contributor.author Schweinfurth, David
dc.contributor.author Sarkar, Biprajit
dc.contributor.author Elumalai, Palani
dc.contributor.author Gupta, Deepak
dc.contributor.author Hussain, Firasat
dc.contributor.author Krishnamoorthy, Govindarajan
dc.contributor.author Sathiyendiran, Malaichamy
dc.date.accessioned 2022-03-27T08:35:56Z
dc.date.available 2022-03-27T08:35:56Z
dc.date.issued 2014-01-21
dc.description.abstract The semirigid ligands 1,4-bis(2-(2-hydroxyphenyl)benzimidazol-1-ylmethyl) benzene (H2-pBC) and 1,3-bis(2-(2-hydroxyphenyl)benzimidazol-1- ylmethyl)-2,4,6-trimethylbenzene (H2-mBC), containing two hydroxyphenylbenzimidazolyl units as bis-chelating (or bis(bidentate)) Nâ̂©OH donor, were synthesized and were used to assemble neutral, luminescent heteroleptic, unsaturated double-hetero-stranded, rhenium(I)-based helicate (1) and mesocate (2) with the flexible bis(monodentate) nitrogen donor (1,4-bis(benzimidazol-1-ylmethyl)benzene/1,3- bis(benzimidazol-1-ylmethyl)benzene), and Re2(CO)10. The photophysical properties of the complexes were studied. Both complexes 1 and 2 exhibit dual emissions in both solution and solid state. In solution, these complexes show both fluorescence and phosphorescence. Complex 1 undergoes a predominantly ligand-centered oxidation, resulting in the generation of phenoxyl radicals. © 2014 American Chemical Society.
dc.identifier.citation Inorganic Chemistry. v.53(2)
dc.identifier.issn 00201669
dc.identifier.uri 10.1021/ic4023135
dc.identifier.uri https://pubs.acs.org/doi/10.1021/ic4023135
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11124
dc.title Luminescent dirhenium(I)-double-heterostranded helicate and mesocate
dc.type Journal. Article
dspace.entity.type
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