RuII–Carbonyl photoCORMs with N,N-Benzimidazole Bidentate Ligands: Spectroscopic, Lysozyme Binding Affinity, and Biological Activity Evaluation

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Abstract

The photoinduced carbon monoxide releasing properties of pyridylbenzimidazole-based RuII–carbonyl complexes functionalized with alkylated sulfonate (LSO3H), phthalimide (LPhth), and morpholine (Lmorph) moieties, [RuCl(CO)3LSO3H]Cl (1) and [RuCl2(CO)2L] {where L = LPhth (2) and Lmorph (3)}, are reported. The geometrical stereochemistry and electronic transitions are assigned with the aid of DFT and TDDFT calculations. The compounds are evaluated for potential antimicrobial and cytotoxic active properties [against noncancerous human embryonic kidney cells (HEK293)]. Complex 2 shows interesting antifungal activity towards Candida albicans and Cryptococcus neoformans, with a similar MIC value of 24 nm. Metalation of hen egg-white lysozyme (HEWL), as a biocompatible carrier, is studied in the dark and upon exposure to light. Stable protein adducts, capable of release CO upon illumination, are formed.

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Mansour, A. M. (2018). RuII–Carbonyl photoCORMs with N,N-Benzimidazole Bidentate Ligands: Spectroscopic, Lysozyme Binding Affinity, and Biological Activity Evaluation. European Journal of Inorganic Chemistry, 2018(7), 852–860. https://doi.org/10.1002/ejic.201701341

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