Introducing magnetic coupling between lanthanide ions has been shown to yield better-performing single-molecule magnets (SMMs), as exemplified by the (CpiPr5)2Ln2I3family of compounds (CpiPr5: pentaisopropylcyclopentadienyl, Ln: Gd, Tb, or Dy). This unique coupling is mediated through an unpaired electron hosted in a σ-like orbital, that results from the two 5dz2 Ln ions, and understanding these interactions holds the key to continue advancing the rational design of SMMs. Here, we focus on the (CpiPr5)2Gd2I3 spin-only system and apply a recently proposed DFT-based decomposition scheme to assess the chemical and structural factors that affect the magnetic coupling. Based on these, we propose synthetically feasible systems with increased coupling.

This article is Open Access

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