Mn-Anderson based polyoxometalate clusters with different terminal groups have been patterned successfully onto self-assembled monolayer (SAM) using microcontact printing. Studies of the interactions between the designed SAMs and human fibroblast (hTERT-BJ1) cells have been reported, and it was observed that cells attach and spread efficiently for monolayer presenting a terminal aromatic pyrene platform with a polyoxometalate Mn-Anderson cluster as linker, demonstrating the crucial role played by the polyoxometalate metal oxide cluster as an intermediary in cell adhesion to the surface.

The synthetic engineering of anionic polyoxometalate (POM) clusters with predefined properties tailored to specific applications is a great challenge using routine "one-pot" POM syntheses. Under such conditions, difficulties often arise from the multitude of complex reaction pathways and self-assembly processes occurring in solution. In this respect the major role of the charge balancing cations cannot be ignored, in fact such cations are crucial, both in the assembly of the building blocks, linkage to the overall cluster, and then assembly into the bulk material. Further, the role of the cation facilitating the selective crystallization of a particular cluster type cannot be divorced from the reaction process since the crystallization process itself can help pull "virtual" building blocks into being. This perspective briefly outlines our efforts towards engineering novel POM based materials, highlighting the use of large organic cations as "Shrink-wrapping" agents to isolate new POM clusters, frameworks and cage compounds. Central to this perspective is the hypothesis that, in the case of POM cluster assembly, the mechanism and various equilibria which define the clusters can be controlled by the selective crystallisation using cation control. Consequently, this indicates that the process of crystallisation can have a profound effect on self-assembly at the molecular level. We therefore propose that the crystallization process itself may define the molecular structure of the cluster leading to the conundrum, which came first, the cluster or the crystal of the cluster?

Connecting clusters: A new class of approximately 3.4 nm sized inorganic–organic–inorganic hybrids was synthesized by covalent functionalization of V3‐capped Wells–Dawson‐type clusters with linear bis(Tris) ligands (see scheme; TBA=nBu4N+). These hybrids were characterized using single‐crystal XRD and ESI‐MS techniques. Dynamic light scattering studies revealed the surfactant properties of these compounds, which lead to the formation of supramolecular vesicles in solutions.

Three organic-inorganic hybrid Mn-Anderson polyoxometalates (POMs), with both symmetrical and asymmetrical appended groups, have been synthesized, identified using electrospray mass spectrometry, and isolated using an approach that allows the three AA, BB, and AB compounds to be structurally characterized. Investigation of the self-assembly of the hybrids on hydrophilic surfaces reveals the formation of nanofibres with characteristics that reflect the nature of the substitution of the POM yielding a route to the programmed assembly of anisotropic hybrid nanostructures.