Education and Training
- Ph.D., Duke University, 1999
Ferrer-Sueta, G., I. Batinić-Haberle, I. Spasojević, I. Fridovich, and R. Radi. “Catalytic scavenging of peroxynitrite by isomeric Mn(III) N-methylpyridylporphyrins in the presence of reductants.” Chem Res Toxicol 12, no. 5 (May 1999): 442–49. https://doi.org/10.1021/tx980245d.
Spasojevic, Ivan, Sandra K. Armstrong, Timothy J. Brickman, and Alvin L. Crumbliss. “Electrochemical Behavior of the Fe(III) Complexes of the Cyclic Hydroxamate Siderophores Alcaligin and Desferrioxamine E.” Inorg Chem 38, no. 3 (February 8, 1999): 449–54. https://doi.org/10.1021/ic980635n.
Batinić-Haberle, I., I. Spasojević, P. Hambright, L. Benov, A. L. Cmmbliss, and I. Fridovich. “Relationship among redox potentials, proton dissociation constants of pyrrolic nitrogens, and in vivo and in vitro superoxide dismutating activities of manganese(III) and iron(III) water-soluble porphyrins.” Inorganic Chemistry 38, no. 18 (January 1, 1999): 4011–22. https://doi.org/10.1021/ic990118k.
Batinić-Haberle, I., L. Benov, I. Spasojević, and I. Fridovich. “The ortho effect makes manganese(III) meso-tetrakis(N-methylpyridinium-2-yl)porphyrin a powerful and potentially useful superoxide dismutase mimic.” J Biol Chem 273, no. 38 (September 18, 1998): 24521–28. https://doi.org/10.1074/jbc.273.38.24521.
Batinić-Haberle, I., I. Spasojević, Y. Jang, R. A. Bartsch, and A. L. Crumbliss. “Lariat Ether Carboxylic Acids as Ionizable Hosts in the Second Coordination Sphere of the Siderophore Ferrioxamine B in Chloroform.” Inorganic Chemistry 37, no. 7 (January 1, 1998): 1438–45. https://doi.org/10.1021/ic970925o.
Batinić-Haberle, I., S. I. Liochev, I. Spasojević, and I. Fridovich. “A potent superoxide dismutase mimic: manganese beta-octabromo-meso-tetrakis-(N-methylpyridinium-4-yl) porphyrin.” Arch Biochem Biophys 343, no. 2 (July 15, 1997): 225–33. https://doi.org/10.1006/abbi.1997.0157.
Batinić-Haberle, I., I. Spasojević, and A. L. Crumbliss. “Solvent effect on second-sphere coordination of ferrioxamine B with substituted 18-crown-6 and 30-crown-10 crown ethers in dichloromethane as compared to chloroform.” Inorganica Chimica Acta 260, no. 1 (July 15, 1997): 35–41. https://doi.org/10.1016/S0020-1693(96)05528-4.