A series of mono- and dinuclear Ru(bpy)2
complexes (bpy = 2,2‘-bipyridine) containing
2,2‘-bis(benzimidazol-2-yl)-4,4‘-bipyridine (bbbpyH2) were prepared. The
mononuclear complex
[Ru(bpy)2(bbbpyH2)](ClO4)2·CH3OH·4H2O was characterized by an X-ray structure
determination. Crystal data are as follows: triclinic,
space
group P1̄, a = 14.443(4) Å,
b = 15.392(4) Å, c = 11.675(2)Å,
α = 101.44(2)°, β = 107.85(2)°, γ =
96.36(2)°,
V = 2380(1) Å3, Z = 2.
The coordination geometry of the ruthenium(II) ion is
approximately octahedral. The
dihedral angle between the two pyridyl rings in bbbpyH2 is
9.4(3)°, which is close to coplanar, in the
complex.
Mono- and dinuclear complexes exhibit broad charge-transfer
absorption bands at 420−520 nm and emission at
660−720 nm in CH3CN solution with lifetimes of
200−800 ns at room temperature. Transient difference
absorption
spectra and resonance Raman (rR) spectra were used to assign the
charge-transfer bands in the 420−520 nm
region and to identify the lowest excited states. Both absorption
and emission spectra are sensitive to solvent
and solution pH. Deprotonation of the dinuclear complex raises the
energies of the π* orbitals of the bbbpyH2
ligand, so that they become closer in energy to the π* orbitals of
bpy. The intervalence band of
[(bpy)2Ru(bbbpyH2)Ru(bpy)2]5+
is observed at 1200 nm ( ε = 170
M-1 cm-1) in
CH3CN. The value of the electronic
coupling matrix element, H
AB, was determined as
120 cm-1. Upon deprotonation, the IT
band was not observed.
It is therefore concluded that a superexchange pathway occurs
predominantly via the Ru(II) dπ−bbbpyH2
π*
interaction, since deprotonation decreases the interaction. The
role of the intervening fragments in the bridging
ligand is discussed from the viewpoint of orbital energies and their
orbital mixing with Ru dπ orbitals.
Protonation and deprotonation of Brönsted basic sites in the tetranuclear RuOs3 complex shown schematically below results in switching between two oxidation patterns A and B. In the deprotonated RuIIIOs 3II complex obtained after one‐electron oxidation, electron transfer from the peripheral OsII atoms to the central RuIII site is induced by the addition of protons. bpy = 2,2′‐bipyridine, — = 2,2′‐bis(benz‐imidazol‐2‐yl)‐4,4′‐bipyridine.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.