Ym. Chiou et L. Que, MODELS FOR ALPHA-KETO ACID-DEPENDENT NONHEME IRON ENZYMES - STRUCTURES AND REACTIVITY OF [FE-II(L)(O(2)CCOPH)](CLO4) COMPLEXES, Journal of the American Chemical Society, 117(14), 1995, pp. 3999-4013
The first iron(II)-alpha-ketocarboxylate complexes were synthesized wi
th the use of tetradentate tripodal ligands tris[(6-methyl-2-pyridyl)m
ethyl] amine (6TLA) and tris(2-pyridylmethyl)amine (TPA) and benzoylfo
rmate (BF) as the alpha-keto acid to model the putative iron-cofactor
interaction in the active site of alpha-keto acid-dependent non-heme i
ron enzymes. [Fe-II(6TLA)(BF)](ClO4) (1) crystallizes in the triclinic
system, space group P (1) over bar (no. 2) with cell constants a 8.93
1(6) Angstrom, b = 13.366(7) Angstrom, c = 15.160(7) Angstrom, alpha =
75.92(4)degrees, beta = 81.06(5)degrees, gamma = 70.78(5)degrees, V =
1652(4) Angstrom(3), and Z = 2; R = 0.071 and R(W) = 0.082. [Fe-II(TP
A)(BF)(MeOH)](ClO4). 2MeOH (2 . MeOH) crystallizes in the orthorhombic
system, space group Pca2(1) (no. 29) with cell, constants a = 19.875(
6) Angstrom, b = 8.916(4) Angstrom, c = 18.02(1) Angstrom, V = 3193(4)
Angstrom(3), and Z = 4; R = 0.054 and R(W) = 0.056. The BF ligand che
lates to the iron in 1 via one carboxylate oxygen and the carbonyl oxy
gen, but binds to the iron in 2 only through a carboxylate oxygen, wit
h a methanol solvate occupying the other site. Both complexes react wi
th dioxygen and quantitatively convert to decarboxylated complexes [Fe
-II(6TLA)(OBz)](+) (5) and [(Fe2O)-O-III(TPA)(2)(OBz)(2)](2+) (6), res
pectively. Both 1 and 2 react with substrates 2,4-di-tert-butylphenol
and triphenylphosphine under an O-2 atmosphere to afford the correspon
ding biphenol and OPPh(3), respectively. O-18(2)-labeling experiments
show incorporation of one O-18 atom into the respective benzoate produ
cts and one into the OPPh(3). Kinetic studies on a series of [Fe-II(6T
LA)(X-BF)](ClO4) complexes show pseudo-first-order disappearance of th
eir characteristic color in the presence of excess dioxygen. The rate
of the oxidative decarboxylation is sensitive to the nature of the phe
nyl substituent, exhibiting a Hammett rho value of +1.07 which indicat
es a nucleophilic mechanism. A reaction mechanism is proposed consisti
ng of dioxygen binding to the iron(II) center, forming an iron(III)-su
peroxide species, attack of the nascent superoxide on the BF keto carb
on, oxidative decarboxylation affording the oxidizing species, and sub
strate oxidation. Complexes 1 and 2 represent the first structural and
functional models for alpha-keto acid-dependent non-heme iron enzymes
.