Spin-Crossover in a New Iron(II)/Di(pyrazolyl)pyridine Complex with a Terpyridine Embrace Lattice. Thermally Induced Excited Spin State Trapping and Clarification of a Structure–Function Correlation

Abstract

The complex salts [FeL2]X2 (1X2; L = 2,6-di{4-fluoropyrazol-1-yl}pyridine; X– = BF4– or ClO4–) exhibit abrupt spin-transitions with narrow thermal hysteresis, at T1/2 = 164 K (X– = BF4–) and 148 K (X– = ClO4–). The transition in 1[ClO4]2 is complicated by efficient thermally induced excited spin-state trapping (TIESST) of its high-spin state below ca. 120 K, and the fully low-spin state was achieved only inside the magnetometer at a scan rate of 0.5 K min–1. Crystals of 1[BF4]2 are tetragonal (P421c, Z = 2; phase 1) at 300 K but transform to a highly twinned monoclinic phase 2 (P21, Z = 2) at 285 ± 5 K. These are forms of the “terpyridine embrace” crystal lattice, which often affords cooperative spin-transitions in iron/di(pyrazolyl)pyridine complexes. Phase 2 of high-spin 1[BF4]2 shows a significant temperature dependence by powder diffraction, which reflects increased canting of the monoclinic unit cell as the temperature is lowered. In contrast, 1[ClO4]2 retains phase 2 between 100 and 300 K, and was crystallographically characterized in its thermally trapped metastable high-spin state at 100 K, as well as its thermodynamic high- and low-spin forms at higher temperatures. The spin-crossover transition temperature in 1[ClO4]2 and related compounds correlates well with a parameter describing angular changes to the metal coordination sphere during the transition but not with other commonly used structural indices. The TIESST metastable high-spin state of 1[ClO4]2 shows no single molecule magnet properties at 2 K.