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Photosubstitution of Monodentate Ligands from Ru II –Dicarboxybipyridine Complexes
Author(s) -
Caraballo Rolando M.,
Rosi Pablo,
Hodak José H.,
Baraldo Luis M.
Publication year - 2017
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201700439
Subject(s) - chemistry , denticity , carboxylate , pyridine , photochemistry , ligand (biochemistry) , quantum yield , bipyridine , excited state , chelation , stereochemistry , crystallography , medicinal chemistry , inorganic chemistry , crystal structure , fluorescence , biochemistry , receptor , physics , quantum mechanics , nuclear physics
We report the photophysical and photochemical properties of Ru II –polypyridine complexes [Ru(bpy)(dcbpy)py 2 ] 2+ ( 1 ) 2+ and [Ru(dcbpy) 2 py 2 ] 2+ ( 2 ) 2+ (bpy = 2,2′‐bipyridine, dcbpy = 4,4′‐dicarboxy‐2,2′‐bipyridine, py = pyridine). These complexes combine a monodentate ligand with a chelate bipyridine substituted with carboxylate groups. At low pH, both complexes present metal‐to‐ligand charge transfer absorption bands in the visible region and room‐temperature photoluminescence with long excited‐state lifetimes ( τ > 200 ns). At physiological pH, their absorption and emission maxima are displaced to higher energies, with a significant reduction of their emission lifetime. These species show photosubstitution of the monodentate pyridine upon irradiation at 450 nm. At low pH, the quantum yield for this process is very low, but at physiological pH, they are very active, with a φ PS,450 value of 0.14 for ( 1 ) 2+ and of 0.17 for ( 2 ) 2+ . The products of photosubstitution were identified as monoaquo complexes. Both the reactants and the products of the photosubstitution show photoluminescence, but with very different lifetimes, making it possible to monitor the reaction by the time constant of their decay. The ability of complexes ( 1 ) 2+ and ( 2 ) 2+ to photorelease monodentate ligands at physiological pH makes them attractive candidates for the delivery of biomolecules linked to more complex structures through the carboxylate functional group.