Dynamic Construction and Maintenance of Confined Nanoregions via Hydrogen-Bond Networks between Acetylene Reactants and a Polyoxometalate-Based Metal-Organic Framework

The nanoconfinement effect in catalysis has attracted much attention because it provides a novel means of regulating the molecular properties and related reactions. Confined nanoregions composed of both reactants and catalysts through weak interactions are expected to improve the catalytic performance and promote the mass transport of relevant molecules simultaneously. However, at reaction temperatures, the structural variation of such confined spaces constructed via weak interactions remains unclear. Herein, through density functional theory calculations combined with ab initio molecular dynamics simulations, we have systematically investigated the dynamic structural evolution of the confined space constructed by acetylene reactants and a polyoxometalate-based metal-organic framework (POMOF) via hydrogen-bond networks. It is found that, at the reaction temperature of acetylene semihydrogenation, the hydrogen bond networks and generated confined nanoregions are not rigid but are constantly changing and dynamically maintained. The steering role played by the O atoms at the surfaces of the polyoxometalate clusters is essential for generation of the hydrogen-bond networks and maintenance of the nanoregions. Upon confinement, the acetylene reactants can be better activated than those in an unconstrained atmosphere, which is reflected by the different dynamic distributions of the angle CHC bending magnitude. Moreover, from a comparison of the distinct interaction characteristics between acetylene/ethylene and POMOF, the different manifestations in the adsorption energy variations of the confined molecules can be interpreted. This work helps to elucidate the underlying mechanisms of confined catalysis and may promote its application in practical catalytic processes.

Automated summary

This study systematically investigated the dynamic structural evolution of a confined space constructed by acetylene reactants and a polyoxometalate-based metal-organic framework (POMOF) via hydrogen-bond networks. It was found that the hydrogen bond networks and generated confined nanoregions are constantly changing and dynamically maintained at the reaction temperature. The O atoms at the surfaces of the polyoxometalate clusters play an essential role in the generation of the hydrogen-bond networks and the maintenance of the nanoregions. Confinement can better activate the acetylene reactants, with different dynamic distributions of the angle CHC bending magnitude.