Strong hydrogen bonds such as F···H···F offer new strategies to fabricate molecular architectures exhibiting novel structures and properties. Along these lines and, to potentially realize hydrogen-bond mediated superexchange interactions in a frustrated material, we synthesized [HF][NiF(Fpy)][SbF] (Fpy = 3-fluoropyridine). It was found that positionally-disordered HF ions link neutral NiF(Fpy) moieties into a kagome lattice with perfect 3-fold rotational symmetry. Detailed magnetic investigations combined with density-functional theory (DFT) revealed weak antiferromagnetic interactions (J ~ 0.4 K) and a large positive-D of 8.3 K with m = 0 lying below m = ±1. The observed weak magnetic coupling is attributed to bond-disorder of the HF ions which leads to disrupted Ni-F···H-F-H···F-Ni exchange pathways. Despite this result, we argue that networks such as this may be a way forward in designing tunable materials with varying degrees of frustration.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5856763PMC
http://dx.doi.org/10.1038/s41598-018-23054-6DOI Listing

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