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90 R. S. Yalow, S. A. Berson, J. Clin. Invest. 1960, 39, 1157–1175. 91 R. S. Yalow, S. A. Berson, Nature 1959, 84, 1648–1649. 92 R. Edwards, in Immunoassay, William Heinemann Medical Books, London, 1985. 93 T. J. Gill, L. T. Mann, J. Immunol. 1965, 96, 906–912. 94 J. P. Gosling, Clin. Chem. 1990, 36, 1408–1427. 95 L. J. Kricka, in Ligand–Binder Assay, Marcel Dekker, New York, 1985. 96 M. Cais, S. Dani, Y. Eden, O. Gandolfi, M. Horn, E. E. Isaacs, Y. Josephy, Y. Saar, E. Slovin, L. Snarsky, Nature 1977, 270, 534–535.

According to the Hieber-base reaction, it is suggested that hydroxide (from iron) attacks a Ni coordinated CO ligand to give a metallocarboxylic acid which decomposes to give CO2 [133]. The original Hieber-base reaction involves the reaction of Fe(CO)5 with hydroxide [176] (Eq. 6). 6) This reaction was reported in 1932 and led to the first carbonyl metal hydride, H2Fe(CO)4. The Hieber-base reaction was first interpretated by Kruck [177], and it is now the accepted mechanism for the metal-catalyzed water gas shift reaction (Eq.

However, the anaerobic oxidation of methane has also been reported [179b]. Finding good organometallic models able to take into account the behavior of organometallic enzymes remains a major goal for the chemist. At present the particular relevance of the model chosen often proves to be a key consideration. Novel multidisciplinary approaches are starting to appear, however, and their complexity may provide new sources of inspiration for research. As an example, Böck recently posed the following question: how did nature tame toxic ligands such as CO and CN– so as to fix them on the iron atoms of hydrogenases?

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