Influence of the solvent on the surface-enhanced raman spectra of ruthenium(II) bipyridyl complexes.

In the present work a new dye, [Ru(dcbpyH2)2(bpy-TPA2)](PF6)2, and the well-known (Bu4N)2[Ru(dcbpyH)2(NCS)2] complex were investigated. The electronic transitions of both dyes showed solvatochromic shifts due to specific interactions of the ligands with the solvent molecules. The surface-enhanced Raman (SER) spectra of the dyes dissolved in water, ethanol, and acetonitrile were measured in silver and gold colloidal solutions. The results demonstrate that the dyes were adsorbed on the metallic nanoparticles in different ways for different solvents. It was also found that in the gold colloid, the aqueous solutions of both dyes did not produce any SERS signal, whereas in ethanolic solution the SERS effect was very weak. Deprotonation, H-bonding, and donor-acceptor interactions seem to determine these different behaviors. Our results indicate the important role of the charge-transfer mechanism in SERS.