Comparative photo-release of nitric oxide from isomers of substituted terpyridinenitrosylruthenium(II) complexes: experimental and computational investigations?

摘要

The 4’-(2-fluorenyl)-2,2’:6’,2’’-terpyridine (FT) ligand and its cis(Cl,Cl)- and trans(Cl,Cl)-[Ru~(_(II))(FT)Cl_2(NO)]-(PF_6) complexes have been synthesized. Both isomers were separated by HPLC and fully characterized by ~1H and ~(13)C NMR. The X-ray diffraction crystal structures were solved for FT (Pna2_1 space group, a = 34.960(4), b = 5.9306(7), c = 9.5911(10) ?), and trans(Cl,Cl)-[Ru~(_(II))(FT)Cl_2(NO)](PF_6)·MeOH (P1 space group, a = 10.3340(5), b = 13.0961(6), c = 13.2279(6) ?, α = 72.680(2), β = 70.488(2), γ = 67.090(2)°). Photorelease of NO? radicals occurs under irradiation at 405 nm, with a quantum yield of 0.31 and 0.10 for cis-(Cl,Cl)-[Ru~(_(II))(FT)Cl_2(NO)](PF_6) and trans(Cl,Cl)-[Ru~(_(II))(FT)Cl_2(NO)](PF_6), respectively. This significant difference is likely due to the trans effect of Cl~?, which favors the photo-release. UV-visible spectroscopy and cyclic voltammetry indicate the formation of ruthenium(_(III)) species as photoproducts. A density functional theory (DFT) analysis provides a rationale for the understanding of the photo-physical properties, and allows relating the weakening of the Ru–NO bond, and finally the photo-dissociation, to HOMO → LUMO excitations.