The syntheses of 2,6-bis(4-chloropyrazol-1-yl)pyridine (L1), 2,6-bis(4-bromopyrazol-1-yl)pyridine (L2) and 2,6-bis(4-iodopyrazol- 1-yl)pyridine (L3) by electrophilic halogenation of 2,6-bis(pyrazol-1-yl)pyridine are reported. The complex [Fe(L1) 2][BF4]2 crystallises in two different solvent-free polymorphs. The tetragonal (α) form crystallises in a known version of the "terpyridine embrace" structure, and undergoes an abrupt spin-transition at 202 K. The orthorhombic (β) form exhibits a modified form of the same packing motif, containing two unique iron sites in a 2: 1 ratio. One-third of the complex molecules in that material undergo a very gradual thermal spin-crossover centred at 137 K. Comparison of the two structures implies that spin-crossover cooperativity in the α-polymorph is transmitted in two dimensions within the extended lattice. [Fe(L 2)2][BF4]2 is isostructural with α-[Fe(L1)2][BF4]2 and exhibits a similarly abrupt spin-transition at 253 K. In contrast, [Fe(L 3)2][BF4]2 is low-spin as a powder at 360 K and below and can be crystallised as two different solvates from acetone solution. All three compounds exhibit the LIESST effect at 10 K, with photoconversions of 40-100%. Their LIESST relaxation temperatures obey the empirical T(LIESST) = T0- 0.3T1/2 (T0 = 150 K) law that we have previously proposed for this class of compound. © The Royal Society of Chemistry 2009.