Nitric oxide (NO) photo-release in a series of ruthenium-nitrosyl complexes: new experimental insights in the search for a comprehensive mechanism

A series of four ruthenium(ii) complexes built from the [Ru(terpy)(bipy)(NO)](3+) core (terpy is 2,2:6,2-terpyridine and bipy is 2,2-bipyridine) are investigated. They differ by the presence of zero, one, two, or three 4-(4-methoxyphenyl) (MP) electron donor substituents introduced at different positions on the pyridine fragments to increase the intramolecular charge transfer capabilities towards the strongly withdrawing nitrosyl (NO) ligand. The UV-visible spectra reflect the presence and position of the MP substituents on the complexes. In the case of species containing the 4-(MP)-terpy ligand, a low-lying transition is identified as arising from 4-(MP)-terpy to Ru(NO) intramolecular charge transfer, which is further confirmed by TD-DFT analysis. Irradiation performed at = 436 nm on this isolated transition for different complexes leads to quantum yields of NO photo-release equal to 0.002 and 0.011, in a ratio of 6 (instead of 1), which allows concluding non-ambiguously that a single electron transition cannot account for the NO release mechanism.