Ranelate ion, the major component of an old antiosporotic drug, exhibits a unusual chemical structure encompassing a thiophene ring with two carboxylic groups, a cyanonitrile substituent, and a nitrile diacetate group; it undergoes decarboxylation at the thiophene carbon‐5 position in acidic solutions, yielding a photoreactive (H5Ran) species which converts into a remarkably stable blue dithiophene dye in the presence of UV light and air.

Ranelate ions, employed in the past as strontium salt for the treatment of osteoporosis, exhibit a rather interesting chemistry associated with a central thiophene ring encompassing two carboxylic groups, a cyanonitrile substituent, and a nitrile diacetate group. In spite of their unfavorable reduction potentials, around 1.26 V, they react very rapidly with HAuCl4 at room temperature, leading to decarboxylation at the C5 position in order to generate gold nanoparticles strongly stabilized by Au–C bonds. The reactions were elucidated by electrospray ionization mass spectrometry, ligand exchange kinetics, and by means of the surface‐enhanced Raman scattering effect. The gold nanoparticles were further characterized based on transmission electron microscopy and CytoViva hyperspectral microscopy.

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Ranelate ion, an old antiosporotic drug, readily reacts with gold(III) ions generating stable gold nanoparticles (AuNP@Ran). The reaction proceeds rapidly under green conditions and is specific for gold ions at...

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