Carboxylate-bridged diiron(II) complexes with a sterically hindered phthalazine ligand

Abstract

The synthesis and crystallographic characterization of a series of diiron(II) complexes with a sterically hindered bridging phthalazine ligand are presented. The carboxylate-bridged compounds [Fe2(μ-O2CR)2(Ph4bdptz)]2+ (R=CH3 (3); C2H5 (4); CH2Ph (5); t-C4H9 (6)), where Ph4bdptz is the ligand 1,4-bis[bis(6-phenyl-2-pyridyl)methyl]phthalazine, and the phosphodiester-bridged complex [Fe2(μ-O2P(OPh)2)2(Ph4bdptz)]2+ (7) were prepared as small molecule models of the catalytic sites in non-heme carboxylate-bridged diiron enzymes. The phenyl rings of Ph4bdptz form a hydrophobic size-constrained pocket in which additional ligands can be accommodated, and they block the possible formation of tetranuclear species. As the steric bulk of the ancillary ligands is increased, the carboxylates shift from a syn, anti to a syn, syn coordination mode. The Mössbauer spectra of the diiron(II) compounds clearly reflect the symmetry of the iron coordination environment.