Synthesis and characterization of imidazolate-bridged dinuclear complexes as active site models of Cu,Zn-SOD

Hideki Ohtsu, Yuichi Shimazaki, Akira Odani, Osamu Yamauchi, Wasuke Mori, Shinobu Itoh, Shunichi Fukuzumi

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New dinucleating ligands having two metal-binding sites bridged by an imidazolate moiety, Hbdpi and HMe4bdpi (Hbdpi = 4,5-bis(di(2- pyridylmethyl)aminomethyl)imidazole, HMe4bdpi = 4,5-bis(di(6-methyl-2- pyridylmethyl)aminomethyl)imidazole), have been designed and synthesized as model ligands for copper-zinc superoxide dismutase (Cu,Zn-SOD). The corresponding mononucleating ligand, MeIm(Py)2 (MeIm(Py)2 = ((1-methyl-4- imidazolyl)methyl)bis(2-pyridylmethyl)amine), has also been synthesized for comparison. The imidazolate-bridged Cu(II)-Cu(II) homodinuclear complexes represented as [Cu2(bdpi)(CH3CN)2](ClO4)3·CH3CN·3H2O (1), [Cu2(Me4bdpi)(H2O)2](ClO4)3·4H2O (2), a Cu(II)-Zn(II) heterodinuclear complex of the type of [CuZn(bdpi)(CH3CN)2](ClO4)3·2CH3CN (3), and a Cu(II) mononuclear complex of [Cu(MeIm(Py)2(CH3CN)](ClO4)2·CH3CN (4) have been synthesized, and the structures of complexes 1 - 4 were determined by X-ray crystallography. The Cu(II)-Zn(II) distance of 6.197(2) Å in 3 agrees well with that of native Cu,ZnSOD (6.2 Å). All the metals in 1 - 4 have pentacoordinate geometries with the imidazolate or 1-methylimidazole nitrogen, two pyridine nitrogens, the tertiary amine nitrogen, and a solvent (CH3CN or H2O). The coordination site occupied by a solvent can be susceptible to ligand substitution, providing a binding site for substrate superoxide. Magnetic measurements of the Cu(II)-Cu(II) homodinuclear complexes 1 and 2 have shown an antiferromagnetic exchange interaction with a coupling constant of -2J = 73.4 and 145.9 cm-1, respectively. The ESR spectra of 1 and 2 exhibited broad signals centered at g ≃ 2.13 due to the spin - spin interaction between two copper ions, while the ESR spectrum of the Cu(II)-Zn(II) heterodinuclear complex 3 showed a signal which is characteristic of mononuclear trigonal-bipyramidal Cu(II) complexes (g is parallel with = 2.10, g is perpendicular with = 2.24, |A is parallel with| = 11.7 mT, and |A is perpendicular with| = 12.4 mT). The cyclic voltammograms of homodinuclear complexes (1 and 2) in CH3CN gave two reversible waves which correspond to the Cu(I,I)/Cu(I,II) and Cu(I,II)/Cu(II,II) redox processes: E(1/2) = -0.31 and -0.03 V vs Ag/AgCl for 1 and E(1/2) = -0.29 and +0.12 V vs Ag/AgCl for 2, respectively. On the other hand, the Cu(II) - Zn(II) heterodinuclear complex 3 exhibited one Cu(I)/(II) reversible wave, E(1/20 = -0.03 V vs Ag/AgCl, which is shifted in a positive direction (0.21 and 0.19 V) as compared to those of the corresponding Cu(II) mononuclear complexes. All the examined complexes catalyzed the dismutation of superoxide at biological pH; the SOD activity increased in the order 2 < 1 < 3.

Original languageEnglish
Pages (from-to)5733-5741
Number of pages9
JournalJournal of the American Chemical Society
Issue number24
StatePublished - 21 Jun 2000


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