The black we wear: Why nature selected 5,6‐dihydroxyindole‐2‐carboxylic acid (DHICA) to synthesize (photo)protective eumelanin pigments is an enigma. Synthetic DHICA eumelanin has now been shown to be a highly efficient free‐radical scavenger in the solid state, which is due to a conformationally interrupted π‐electron network associated with atypical optical, paramagnetic, and aggregation properties.
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