Abstract
The generation of noncovalent intermolecular interactions represents a powerful method to control molecular vibrations and rotations. Combining these with the axial ligand field enforced by the metallocene ligand scaffold provides a dual-pronged approach in controlling the magnetic-relaxation pathways for dysprosium-based single-molecule magnets (SMMs). Here, we present the first implementation of 2,3,4,5-tetraiodopyrrole (TIPH) in its anionic form [TIP](-) as a ligand in three isostructural rare-earth metal complexes Cp*(2)RE(TIP) (1-RE, RE = Y, Gd, and Dy; Cp* = pentamethylcylopentadienyl), where the TIP ligand binds through the nitrogen and one iodine atom κ(2)(N,I) to the metal centre. The shallow potential energy surface of the intermolecular σ-hole interaction yields distortions of the interatomic distances at elevated temperatures which were investigated by variable-temperature SCXRD. 1-RE constitute the first crystallographically characterized molecules containing TIP as a ligand for any metal ion, and 1-Dy is the first SMM that employs the TIP ligand. The structural dependence on temperature allowed the mechanism of magnetic relaxation to be explored through ab initio calculations at different temperatures. The electronic influence of the coordinated iodine substituent was probed via magnetometry and cw-EPR spectroscopy on 1-Gd. To further scrutinize the impact of the iodine substituents on the physical properties, a second set of new complexes Cp*(2)RE(DMP) (2-RE, RE = Y, and Dy) where DMP = 2,5-dimethylpyrrolyl were synthesized. Here, the DMP ligand binds similarly to the TIP ligand and represents an all-hydrocarbon analogue to 1-RE. 2-Dy constitutes the first SMM bearing a DMP ligand.