Construction of spin-crossover dinuclear cobalt() compounds based on complementary terpyridine ligand pairing

The self-assembly of multinuclear SCO complexes is appealing in which unique properties may be discovered due to enhanced intramolecular and intermolecular interactions. In this work, three dinuclear cobalt( ii ) complexes, named Co-1 , Co-2 , and Co-3 , were prepared based on a complementary terpyridine ligand pair strategy. The complexes were accurately synthesized by the solvothermal method in which dinuclear complexes were directional assemblies from cobalt( ii ) ions, terpy bearing 2,6-dimethoxyphenyl substituents at the terpyridyl 6,6′′-positions, and ditopic terpy built with different linkers (alkynyl for 1 , diynyl for 2 , and phenyl for 3 ). Single-crystal structure determinations reveal that all compounds possess a central symmetric molecular structure, so that two cobalt( ii ) units are identical in the solid state. Their spin crossover behaviours were investigated through variable-temperature magnetic susceptibility studies. Co-1 undergoes limited SCO with a large population of low spin state ( S = 1/2) in the measured temperatures. Co-2 and Co-3 exhibit solvent-modulated SCO behaviour. Impressively, the de-solvated samples show a repeatable thermal hysteresis loop around the room temperature region. This work demonstrates that complementary terpyridine ligand pairing is a practical approach to accurate and directional construction of multinuclear SCO-active compounds. Three dinuclear cobalt( ii ) SCO-active compounds have been successively prepared employing the strategy of complementary terpyridine ligand pairing.