Anchoring Atomically Precise Chiral Bismuth Oxido Nanoclusters on Gold: The Role of Amino Acid Linkers.

The adsorption of chiral molecules onto metallic surfaces triggers electron spin polarization at the interface, paving the way for applications in chiral opto-spintronics. However, the spin effects sensitively depend on the binding and ordering of the chiral species on surfaces. This study explores the adsorption of chiral thioether-functionalized atomically precise bismuth oxido nanoclusters (BiO-NCs) on gold (Au) surfaces, extending the conventional approach of using thiol-containing molecules and complexes to nanoclusters. Starting from the precursor [BiO(NO)(dmso)](NO)·4dmso (A), chiral BiO-NCs were synthesized by substituting the nitrates with -(-butoxycarbonyl)-l-methionine (Boc-l-Met-O) ligands to obtain [BiO(Boc-l-Met-O)] (). The full exchange of nitrate by the Boc-l-methionine ligand was demonstrated by powder X-ray diffractograms, dynamic light scattering, electrospray ionization mass spectrometry, nuclear magnetic resonance, infrared, circular dichroism, and X-ray photoelectron spectroscopy. Compared to previously reported [BiO(Boc-l-Phe-O)(dmso)] (), BiO-NC shows differences in the growth mode on a Au surface as revealed by scanning electron microscopy, wherefore a stronger binding of BiO-NC is assumed. Anchoring of BiO-NC to the Au surface through thioether groups induced a discernible change in the optical response of the Au surface analyzed by spectroscopic ellipsometry (SE). From the numerical modeling of the SE parameters, a layer thickness of ∼2 nm, corresponding to a monolayer of BiO-NC , was estimated for the samples prepared by dip coating. Thus, strong adsorption of BiO-NC to the Au surface is concluded, which is an essential prerequisite for chiral-induced interface spin polarization.