Clusters in bis-tridentate tethered domains of an iron chelating drug

Abstract

The tridentate metal binding domains of iron chelating agents have been tethered via a variable length methylene (CH2)n linker (n = 1, 2, 4, 6, 8, 10, 14). The single-crystal X-ray structures of monomeric ([Fe(HL8)]·2.5H2O n = 8; H4L8 is 1,10-decanedioyl di(salicylaldehyde hydrazone)) and dimeric ([{Fe(H2PL4)}2]Cl2·2H 2O n = 4; H4PL4 is 1,6-hexanedioyl di(pyridoxal hydrazone)) iron(III) complexes have been determined. The complexes exhibit oligomerism: with chain lengths of n≥6 monomers are prevalent whereas for shorter chains this is not possible and a series of clusters exist as shown by ESMS and molecular modelling. © The Royal Society of Chemistry 1999.