Structure of an iron(II) dioxygen complex; a model for oxygen carrying hemeproteins

The preliminary structural characterization of a reversible ferrous dioxygen complex is reported. Mono(N-methyl imidazole) (dioxygen) meso-tetra (alpha,alpha,alpha,alpha-o-pivalamidephenyl) porphinatorino(II), [Fe(O(2))-(N-Me imid) (alpha,alpha,alpha,alpha-TpivPP)], 1, isolated from toluene solution, crystallizes in the monoclinic system with four molecules in a unit cell of dimensions a = 18.690 (3), b = 19.514 (3), c = 18.638 (3) A, and beta = 91.00 (1) degrees . R = 0.15 for 841 reflections having F(2) > 3sigma (F(2)). The complex 1 has four pivalamido groups on one side of the porphyrin forming a hydrophobic pocket of 5.4-A depth which encloses coordinated dioxygen. The dioxygen is coordinated "end-on," with a bent Fe-O-O bond. The Fe-O-O plane bisects an N-Fe-N right angle of the equatorial iron porphyrin plane and is four way statistically disordered. In addition there is a crystallographic 2-fold axis through iron, coordinated oxygen, and nitrogen of the axially bound N-methyl imidazole. Thus there are two types of coordinated dioxygen with the Fe-O-O plane either parallel or perpendicular to the trans axial imidazole plane. Corresponding values for the Fe-O-O bond angles are 135-(4) degrees and 137(4) degrees and for the O-O bond lengths are 1.23 (0.08) and 1.26 (0.08) A, with a dihedral angle of 90 degrees between alternative orientations of the Fe-O-O plane. The Fe-O distance is 1.75 (0.02) A and Fe-N (imidazole) is 2.07 (0.02) A, suggesting multiple bond character in the Fe-O moiety. The similarity of the Mössbauer spectrum of the model complex, 1, with oxyhemoglobin indicates that 1 may be a good model for oxygen binding in the oxygen transport hemeproteins.