The formation of giant polyoxometalate (POM) species is relatively underexplored, as their selfassembly process is complex due to the rapid kinetics. Polyoxopalladates (POPds) are a class of POMs based on Pd, the largest of which is the {Pd 84 } Ac wheel, and its slower kinetics mean the system is more amenable to systematic study. Here, we show that it is possible to follow the assembly of two types of Pd wheels, {Pd 84 } Gly and the smaller {Pd 72 } Prop , formed using glycolate and propionate ligands, respectively. We analyzed the formation of {Pd 72 } Prop and {Pd 84 } Gly using mass spectrometry (SEC-HPLC-MS and preparative desalting followed by MS). This was accompanied by studies that followed the chemical shift differences between the outer/ inner ligands and the free ligand in solution for the {Pd 84 } Ac , {Pd 72 } Prop , and {Pd 84 } Gly species using NMR, which showed it was possible to track the formation of the wheels. Our findings confirm that the macrocycles assemble from smaller building blocks that react together to form the larger species over a period of days. These findings open the way for further structural derivatives and exploration of their host−guest chemistry. P olyoxometalates (POMs) are metal oxide clusters formed by transition metals like Mo, V, and W that are able to self-assemble in complex, high-nuclearity structures from simple precursors.1 Noble metals Pd, Pt, and Au, and even lanthanides like Ga, can form high-nuclearity metal oxide structures, such as wheel-like {Gd 140 }.2,3 One of the challenges in this field is to understand the assembly process, especially for the systems that form gigantic ring clusters, and only a few mechanistic studies have been explored. These studies have been limited due to the rapid kinetics, 4 and mechanistic data have been restricted to low-nuclearity moieties.5−8 However, the formation of curved units is suggested to be the driving force in the formation of both spherical molybdenum brown Keplerate {Mo 132 } 9−12 and ring-shaped molybdenum blue ring {Mo 154 }.
13To address this issue, we decided to target systems that form gigantic structures but assemble more slowly.14,15 The first of these is a smaller {Pd 72 (Figure 1). This structural analogue contains 28 glycolate ligands in place of acetate. To directly probe the mechanisms of formation of the {Pd 72 } Prop and {Pd 84 } Gly in situ, we used mass spectrometry (MS) and 1 H NMR. However, MS cannot be used to follow the process in the reaction solutions directly due to ion suppression issues arising from the high salt concentration. Therefore, we developed a separation "desalting" step. To do this we used SEC-HPLC-MS to separate the species present in the reaction based on their size. The second method was the direct injection of aliquots of mother liquor which had been prepared by "desalting" in small disposable size-exclusion columns (MicroBioSpin 6).Preliminary studies had suggested that the manual desalting columns are more effective at removing salt from the Pd macrocycle r...