Sub lattice driven spin state ordering and coordination elasticity in Fe(ii) 1,3,4-thiadiazole complexes
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Abstract
Understanding the role of co-ligand identity, governing spin-state energetics in many Fe(ii) complexes, is essential for designing responsive spin-crossover materials. We report the synthesis of an unsymmetrical bis(pyridin-2-ylmethyl)glycyl benzohydrazide-derived ligand, 1-(5-phenyl-1,3,4-thiadiazol-2-yl)-N,N-bis(pyridin-2-ylmethyl)methanamine (LPh-TDA), and its corresponding complexes [Fe(LPh-TDA)(NCE)2]·H2O (E = S (C1), Se (C2), BH3 (C3)). While the ligand-field strength gradient ranges from weak (NCS−) to strong (NCBH3−), the SCO behaviour of the resulting complexes does not reflect this. Variable-temperature single-crystal X-ray diffraction, SQUID magnetometry and 57Fe Mössbauer spectroscopy show that there is packing-induced sublattice spin-state ordering for C1, which has two distinct Fe(ii) sites. Of these sites, only one transitions to the low-spin state in two complexes, while the second remains locked in the high-spin (HS) state. C2 remains high-spin throughout the entire temperature range, whereas C3 exhibits a complete, one-step SCO with T1/2 = 153 K. Density functional theory (DFT) calculations help to quantify the energetic origin of the ordered LS–HS configuration in C1 and demonstrate that intermolecular packing effects override intrinsic ligand-field trends. These results highlight the dominant role of solid-state organization in dictating SCO behavior, even in systems engineered to isolate co-ligand electronic effects.
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Dalton transactions : a journal of inorganic chemistry, including bioinorganic, organometallic, and solid-state chemistry, 55, 7, RSC, Cambridge, 2026, https://doi.org/10.1039/d5dt02912k