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Atomically precise thiol­ate-protected gold nanomolecules have attracted inter­est due to their distinct electronic and chemical properties. The structure of these nanomolecules is important for understanding their peculiar properties. Here, we report the X-ray crystal structure of a 24-atom gold nanomolecule protected by 16 tert-butylthiolate ligands. The com­position of Au24(S-C4H9)16 {poly[hexa­deca­kis­(μ-tert-butyl­thiol­ato)tetra­cosa­gold]} was confirmed by X-ray crystallography and electrospray ionization mass spectrometry (ESI–MS). The nanomolecule was synthesized in a one-phase synthesis and crystallized from a hexa­ne–ethanol layered solution. The X-ray structure confirms the 16-atom core protected by two monomeric and two trimeric staples with four bridging ligands. The Au24(S-C4H9)16 cluster follows the shell-closing magic number of 8. 

Atomically precise thiolate-protected gold nanomolecules have attracted interest due to their distinct electronic and chemical properties. The structure of these nanomolecules is important for understanding their peculiar properties. Here, we report the X-ray crystal structure of a 24-atom gold nanomolecule protected by 16 tert -butylthiolate ligands. The composition of Au 24 (S-C 4 H 9 ) 16 {poly[hexadecakis(μ- tert -butylthiolato)tetracosagold]} was confirmed by X-ray crystallography and electrospray ionization mass spectrometry (ESI–MS). The nanomolecule was synthesized in a one-phase synthesis and crystallized from a hexane–ethanol layered solution. The X-ray structure confirms the 16-atom core protected by two monomeric and two trimeric staples with four bridging ligands. The Au 24 (S-C 4 H 9 ) 16 cluster follows the shell-closing magic number of 8. 

Digestive ripening (DR) is a synthetic method where a polydisperse colloid of metal nanoparticles upon refluxing with a free ligand in a high boiling point solvent gives monodisperse nanoparticles. Brust synthesis is known to form atomically monodisperse thiolate protected gold nanoparticles also known as gold nanomolecules (Au NMs). Unlike the Brust method which gives smaller (1–3 nm) atomically precise nanomolecules, DR has been used only for the synthesis of large nanoparticles (>5 nm) with good monodispersity. In thiolate protected gold nanoparticle Brust synthesis, the yellow colored phase transferred Au( iii ) solution is converted to a colorless Au( i ) mixture after the addition of thiol by forming Au–SR, which is then reduced to form black colored Au NMs. However, in DR, by using the same primary chemicals, the two steps were reversed: the mixture was reduced before the addition of thiol. Here we show that in DR, adding thiol after 2 minutes of reduction gives larger particles (5 nm) as reported, whereas adding thiol 30 seconds after reduction results in smaller particles (<2 nm). In this work, for the first time, DR yields atomically precise Au 25 (SR) 18 and Au 144 (SR) 60 NMs. This is reported using two aliphatic thiols – hexanethiol and dodecanethiol – as the protecting ligands. DR was also repeated using an aromatic thiol, 4- tert -butyl benzene thiol (TBBT), which yields Au 279 (SR) 84 NMs consistent with the Brust method, thereby establishing that both DR and Brust methods lead to the formation of atomically precise Au NMs, regardless of the order of thiol addition and reduction steps.