
Chemists have sought to control positioning of guest atoms in host spaces for the purpose of designing and synthesizing chemical systems with predetermined properties. The natural flexibility of ether molecules has largely prevented this from happening in the case of the crown ether family of structures. In contrast in graphene, crown ether structures are held rigid by the carbon lattice and the ether donor groups are flattened onto the graphene plane in such a way that the dipoles point directly at the center of the binding cavity. Using aberration-corrected scanning transmission electron microscopy and density-functional calculations, we find that the binding properties of these new structures exceed those obtained with individual crown ether molecules.
J. Guo, J. Lee, C. I. Contescu, N. C. Gallego, S. T. Pantelides, S. J. Pennycook, B. A. Moyer, and M. F. Chisholm, “Crown ethers in graphene,” Nature Commun. 5, 5389 (2014). doi: 10.1038/ncomms6389.
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