Ligand engineering of immobilized nanoclusters on surfaces: ligand exchange reactions with supported Au 11 (PPh 3 ) 7 Br 3 Au 11 nanoclusters immobilized on an alumina surface have shown to be accessible to ligand sphere transformations by thiolates in an aqueous environment. In contrast to the same ligand exchange in solution, the number of metal atoms in the core is preserved. This enables modifi cations of the nanocluster's structure and properties even after surface immobilization, e.g., by inducing photoluminescence through binding of fl uorescent thiolates.The properties of gold nanoclusters, apart from being size-dependent, are strongly related to the nature of the protecting ligand. Ligand exchange on Au nanoclusters has been proven to be a powerful tool for tuning their properties, but has so far been limited to dissolved clusters in solution. By supporting the clusters previously functionalized in solution, it is uncertain that the functionality is still accessible once the cluster is on the surface. This may be overcome by introducing the desired functionality by ligand exchange after the cluster deposition on the support material. We herein report the first successful ligand exchange on supported (immobilized) Au 11 nanoclusters. Dropcast films of Au 11 (PPh 3 ) 7 Br 3 on planar oxide surfaces were shown to react with thiol ligands, resulting in clusters with a mixed ligand shell, with both phosphines and thiolates being present. Laser ablation inductively coupled plasma mass spectrometry and infrared spectroscopy confirmed that the exchange just takes place on the cluster dropcast. Contrary to systems in solution, the size of the clusters did not increase during ligand exchange. Different structures/compounds were formed depending on the nature of the incoming ligand. The feasibility to extend ligand engineering to supported nanoclusters is proven and it may allow controlled nanocluster functionalization. † Electronic supplementary information (ESI) available: Detailed description of the experimental procedures, UV-Vis and MALDI-MS spectra of the ligand exchanges in solution, additional MALDI-MS, LA-ICP-MS, PL, PM-IRRAS and ATR-IR spectra of the ligand exchange on the surface, TEM images of the clusters and the discussion of another ligand exchange on the surface with 2-PET under different conditions. See Scheme 1 Left (1): Ligand exchange reactions of Au 11 (PPh 3 ) 7 Br 3 in solution with GSH (1a) and 2-PET (1b). Right (2): Ligand exchange reactions of supported Au 11 (PPh 3 ) 7 Br 3 with GSH (2a) and 2-PET (2b). Color code: Au = , P = , S = , Br = , O = , and N = . The organic ligand framework of the cluster structures after exchange is not shown.