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We report two novel “clickable” [(μ-S2C2H4NR)Fe2(CO)6] complexes and their incorporation into single-chain nanoparticles. Variations in the characteristic iron–carbonyl stretching bands caused by the polymer scaffolds confirmed changes in the symmetry and electronics of the complexes. This represents the first SCNP-based model of a metalloenzyme bearing a single, bioinspired active site.

Graphical abstract: Toward a tunable synthetic [FeFe] hydrogenase mimic: single-chain nanoparticles functionalized with a single diiron cluster

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