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Ancillary Ligand Functionalization of Cyanide-bridged S = 6 Fe^III4Ni^II4 Complexes for Molecule-based Electronics
Inorganic Chemistry (2006)
  • Stephen Holmes, University of Missouri-St. Louis
  • Dongfeng Li, University of Kentucky
  • Sean Parkin, University of Kentucky
  • Rodolphe Clérac, Centre de Recherche Paul Pascal
Abstract
Treatment of 1-chloro-6-iodohexane or 1-chloro-10-iododecane with lithium tris(pyrazolyl)methanide, followed by potassium thioacetate, affords bifunctional 1-S(acetyl)-tris(pyrazolyl)alkanes (L) (pz)3C(CH2)nSAc (n = 6, 1; 10, 2). Magnetic studies of {[(pzTp)FeIII(CN)3]4[NiIIL]4[OTf]4}·solvent (4, L = 15, L = 2) boxes suggest that −(CH2)6 chains (4) limit intermolecular interactions while −(CH2)10 chains in 5 introduce crystallographic disorder and a distribution of relaxation times; 4 and 5 exhibit slow relaxation of magnetization.
Publication Date
2006
DOI
10.1021/ic060695q
Citation Information
Stephen Holmes, Dongfeng Li, Sean Parkin and Rodolphe Clérac. "Ancillary Ligand Functionalization of Cyanide-bridged S = 6 Fe^III4Ni^II4 Complexes for Molecule-based Electronics" Inorganic Chemistry Vol. 45 Iss. 19 (2006) p. 7569 - 7571
Available at: http://works.bepress.com/stephen-holmes/31/