Lanthanide-radical single-molecule magnets: current status and future challenges.

In the field of molecular magnetism, the lanthanide-radical (Ln-Rad) method has become one of the most appealing tactics for introducing strong magnetic interactions and has spurred on the booming development of heterospin single-molecule magnets (SMMs). The article is a timely retrospect on the research progress of Ln-Rad heterospin systems and special attention is invested on low dimensional Ln-Rad compounds with SMM behavior, primarily concerning with nitrogen-based radicals, semiquinone and nitroxide radicals. Rational design, molecular structures, magnetic behaviors and magneto-structural correlations are highlighted.

Improved single-chain-magnet behavior in a biradical-based nitronyl nitroxide-Cu-Dy chain.

A biradical with ferromagnetic intramolecular interaction was found to improve the SCM behavior of a nitronyl nitroxide-Cu-Dy chain, resulting in an energy barrier for magnetization reversal of 40 K.

Gold atomic clusters extracting the valence electrons to shield the carbon monoxide passivation on near-monolayer core-shell nanocatalysts in methanol oxidation reactions.

Atomic-scale gold clusters were intercalated at the inter-facet corner sites of Pt-shell Ru-core nanocatalysts with near-monolayer shell thickness. We demonstrated that these unique clusters could serve as a drain of valence electrons in the kink region of the core-shell heterojunction. As jointly revealed by density functional theory calculations and valence band spectra, these Au clusters extract core-level electrons to the valence band.