Abstract

This work reports on a novel nitrosyl–ruthenium complex bearing the azanaphthalene ligand quinazoline (qui) in its coordination sphere. The product crystallizes with an additional quinazoline molecule, yielding the compound cis-[Ru(bpy) 2(qui)NO](PF 6) 3 · ( qui). This feature leads to an absorption band at λ max = 430 nm in CH 3CN and λ max = 420 nm in phosphate buffer, which promotes the photorelease of nitric oxide under visible light irradiation ( λ > 400 nm), in 1 ethanol:1 water (v/v) mixture or under physiological pH. Both the intensity and energy of this transition are dependent on solvent and solution pH, suggesting that the transition has a charge transfer nature, and that the association of the second quinazoline molecule with the complex is driven by weak interactions, possibly of the π-stacking type.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call