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In particular, redox\u2010stable, easily accessible ligands are decisive. Here, we report a straightforward and facile synthesis of a new highly stable 2,6\u2010bis(triazolyl)pyridine ligand, containing a nitrile moiety as a masked anchoring group, using copper(I)\u2010catalyzed azide\u2010alkyne cycloaddition (CuAAC) click reaction. The reported structure mimics the binding motif of uneasy to synthesize ligands. Pulse radiolysis under oxidizing and reducing conditions provided evidence for the high stability of the formed radical cation and radical anion 2,6\u2010di(1,2,3\u2010triazol\u20101\u2010yl)\u2010pyridine compound, thus indicating the feasibility of utilizing this as a ligand for redox active metal complexes and the sensitization of metal\u2010oxide semiconductors (<jats:italic>e.\u2009g<\/jats:italic>., TiO<jats:sub>2<\/jats:sub> nanoparticles or nanotubes).<\/jats:p>","DOI":"10.1002\/cphc.202400273","type":"journal-article","created":{"date-parts":[[2024,5,31]],"date-time":"2024-05-31T12:34:10Z","timestamp":1717158850000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Synthesis and Photo\/Radiation Chemical Characterization of a New Redox\u2010Stable Pyridine\u2010Triazole Ligand"],"prefix":"10.1002","volume":"25","author":[{"given":"Abdulaziz 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