Understanding Metal-Organic Framework Nucleation from a Solution with Evolving Graphs

A mechanistic understanding of metal???organic framework (MOF) synthesis and scale-up remains underexplored due to the complex nature of the interactions of their building blocks. In this work, we investigate the collective assembly of building units at the early stages of MOF nucleation, using MIL-101(Cr) as a prototypical example. Using large-scale molecular dynamics simulations, we observe that the choice of solvent (water and N,N-dimethylformamide), the introduction of ions (Na+ and F???) and the relative populations of MIL-101(Cr) half-secondary building unit (half-SBU) isomers have a strong influence on the cluster formation process. Additionally, the shape, size, nucleation and growth rates, crystallinity, and short and long-range order largely vary depending on the synthesis conditions. We evaluate these properties as they naturally emerge when interpreting the self-assembly of MOF nuclei as the time evolution of an undirected graph. Solution-induced conformational complexity and ionic concentration have a dramatic effect on the morphology of clusters emerging during assembly. While pure solvents lead to the rapid formation of a small number of large clusters, the presence of ions in aqueous solutions results in smaller clusters and slower nucleation. This diversity is captured by the key features of the graph representation. Principle component analysis on graph properties reveals that only a small number of molecular descriptors is needed to deconvolute MOF self-assembly. Descriptors such as the average coordination number between half-SBUs and fractal dimension are of particulalr interest as they can be can be followed experimentally by techniques like by time-resolved spectroscopy. Ultimately, graph theory emerges as an approach that can be used to understand complex processes revealing molecular descriptors accessible by both simulation and experiment.

Automated summary

In this study, the collective assembly of building units during the early stages of metal-organic framework (MOF) nucleation was investigated using large-scale molecular dynamics simulations. The choice of solvent, introduction of ions, and relative populations of MOF building unit isomers were found to greatly influence the cluster formation process, leading to variations in shape, size, nucleation and growth rates, crystallinity, and order. Graph theory analysis revealed that only a few molecular descriptors were needed to understand MOF self-assembly and these descriptors can be experimentally observed. This approach provides valuable insights into the complex processes of MOF synthesis and scale-up.