PRITCHARD, Ruth; LAZAR, Hanane Z.; BARRET, Simon A.; KILNER, Colin A.; ASTHANA, Saket; CARBONERA, Chiara; LETARD, Jean-François; HALCROW, Malcolm A.

doi:10.1039/b907094j

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PRITCHARD, Ruth
School of Chemistry [Leeds]

LAZAR, Hanane Z.
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]

BARRET, Simon A.
School of Chemistry [Leeds]

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Dalton Transactions. 2009 n° 33, p. 6656-6666

Royal Society of Chemistry

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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 (alpha) form crystallises in a known version of the "terpyridine embrace" structure, and undergoes an abrupt spin-transition at 202 K. The orthorhombic (beta) 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 alpha-polymorph is transmitted in two dimensions within the extended lattice. [Fe(L2)2][BF4]2 is isostructural with alpha-[Fe(L1)2][BF4]2 and exhibits a similarly abrupt spin-transition at 253 K. In contrast, [Fe(L3)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- 0.3T(1/2) (T0 = 150 K) law that we have previously proposed for this class of compound.< Réduire

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Thermal and light-induced spin-transitions in iron(II) complexes of 2,6-bis(4-halopyrazolyl)pyridines: the influence of polymorphism on a spin-crossover compound

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