In this study benzyl and ethyl groups were appended to pyridine and aniline ancillary ligands in diiron(II) complexes of the type [Fe-2(mu-O2CArR)(2)(O2CArR)(2)(L)(2)], where (-O2CArR) is a sterically hindered terphenyl carboxylate, 2,6-di(p-tolyl)- or 2,6-di(p-fluorophenyl)benzoate (R = Tol or 4-FPh, respectively). These crystallographically characterized compounds were prepared as analogues of the diiron(II) center in the hydroxylase component of soluble methane monooxygenase (MMOH). The use of 2-benzylpyridine (2-Bnpy) yielded doubly bridged [Fe-2(mu-O2CArtol)(2)(O2CArTol)(2)(2-Bnpy)(2)] (1) and [Fe-2(mu-O2CAr4-FPh)(2)(O2CAr4-FPh)(2)(2-Bnpy)(2)] (4), whereas tetra-bridged [Fe-2(mu-O2CArTol)(4)(4-Bnpy)(2)] (3) resulted when 4-benzylpyridine (4-Bnpy) was employed. Similarly, 2-(4-chlorobenzyl)pyridine (2-(4-CIBn)py) and 2-benzylaniline (2-Bnan) were employed as N-donor ligands to prepare [Fe-2(mu-O2CArTol)(2)(O(2)CA(Tol))(2)(2-(4-CIBn)py)(2)] (2) and [Fe-2(mu-O2CArTol)(2)(O2CArTol)(2)(2-Bnan)(2)] (5). The placement of the substituent on the pyridine ring had no effect on the geometry of the diiron(II) compounds isolated when 2-, 3-, or 4-ethylpyridine (2-, 3-, or 4-Etpy) was introduced as the ancillary nitrogen ligand. The isolated [Fe-2(mu-O(2)CA(Tol))(2)(O(2)CA)(2)(2-Etpy)] (6), [Fe-2(mu-O2CArTol)(2)(O2CArTol)(2)(3-Etpy)] (7), [Fe-2(mu-O2CArTol)(2)(O2CArTol)(2)(4-Etpy)] (8), and [Fe-2(mu-O2CAr4-FPh)(2)(O2CAr4-FPh)(2)(2-Etpy)(2)] (9) complexes all contain doubly bridged metal centers. The oxygenation of compounds 1-9 was studied by GC-MS and NMR analysis of the organic fragments following decomposition of the product complexes. Hydrocarbon fragment oxidation occurred for compounds in which the substrate moiety was in close proximity to the diiron center. The extent of oxidation depended upon the exact makeup of the ligand set.