Abstract
Redox‐active guanidines are versatile reagents in redox and proton‐coupled electron‐transfer (PCET) reactions. Recently, they were integrated as sacrificial electron donors for the prohibition of metal oxidation in perovskite materials. Herein we report the synthesis and characterization of several new redox‐active guanidines with aromatic (benzene, naphthalene or anthraquinone) cores. Two of these compounds are then integrated in lead iodide materials. The structure, thermal stability and optical band‐gap of the resulting materials are evaluated.
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