SYNTHESES AND CHARACTERIZATION OF MONONUCLEAR AND DINUCLEAR IRON(III)COMPLEXES OF 1,4,7-TRIAZACYCLONONANE-N-ACETATE-(L) - CRYSTAL-STRUCTURES OF [FECL(2)L] AND )CME)L(2)]CLO4-CENTER-DOT-NACLO4-CENTER-DOT-2H(2)O
B. Graham et al., SYNTHESES AND CHARACTERIZATION OF MONONUCLEAR AND DINUCLEAR IRON(III)COMPLEXES OF 1,4,7-TRIAZACYCLONONANE-N-ACETATE-(L) - CRYSTAL-STRUCTURES OF [FECL(2)L] AND )CME)L(2)]CLO4-CENTER-DOT-NACLO4-CENTER-DOT-2H(2)O, Journal of the Chemical Society. Dalton transactions, (5), 1997, pp. 887-893
The macrocycle 1,4,7-triazacyclononane-N-acetate (L) reacted with FeCl
3 . 6H(2)O in water to form the monomeric complex [FeCl(2)L] 1. Hydrol
ysis of 1 in the presence of an excess of sodium acetate and sodium pe
rchlorate yielded the binuclear complex [Fe-2(mu-O)(mu-O(2)CMe)L(2)]Cl
O4 . NaClO4 . 2H(2)O 2. Complexes 1 and 2 have been characterised by X
-ray crystallography. In 1 the Fe-III is surrounded by a distorted-oct
ahedral array of one fac-co-ordinated triamine ring, one monodentate c
arboxylato group and two chloride ligands. Complex 2 consists of a mu-
oxo-mu-acetato-diiron(III) core with the distorted octahedral co-ordin
ation sphere about each Fe-III being completed by the ligand L. A sodi
um ion, with distorted trigonal-bipyramidal stereochemistry, bridges b
etween the coordinating carboxylate oxygens of the terminal ligands. C
omplex 2 exhibits spectroscopic features and magnetic properties simil
ar to those of other mu-oxo-diiron(III) complexes as well as metallopr
oteins incorporating a mu-oxo-diiron(III) unit at their active sites.