Abstract
The syntheses of 4-mercapto-2,6-di(pyrazol-1-yl)pyridine (bppSH) and bis[2,6-di(pyrazol-1-yl)pyrid-4-yl]disulfide (bppSSbpp) are reported. In contrast to previously published "back-to-back" bis-[2,6-di(pyrazol-1-yl)pyridine] derivatives, which form coordination polymers with transition ions that are usually insoluble, bppSSbpp yields soluble oligomeric complexes with iron(ii) and zinc(ii). Mass spectrometry and DOSY data show that [{Fe(μ-bppSSbpp)} n ] 2n+ and [{Zn(μ-bppSSbpp)} n ] 2n+ form tetranuclear metallacycles in nitromethane solution (n = 4), although 1 H NMR and conductivity measurements imply the iron compound may undergo more fragmentation than its zinc congener. Both [{Fe(bppSH) 2 ] 2+ and [{Fe(μ-bppSSbpp)} n ] 2n+ exhibit thermal spin-crossover in CD 3 NO 2 solution, with midpoint temperatures near 245 K. The similarity of these equilibria implies there is little cooperativity between the iron centres in the metallacyclic structures.
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CITATION STYLE
Kershaw Cook, L. J., Fisher, J., Harding, L. P., & Halcrow, M. A. (2015). An iron(ii) spin-crossover metallacycle from a back-to-back bis-[dipyrazolylpyridine]. Dalton Transactions, 44(20), 9417–9425. https://doi.org/10.1039/c5dt00732a
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