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Part of the book series: NATO ASI Series ((ASIC,volume 465))

Summary

The reaction pathway of the oxidation of the [Fe(CO)4]2- dianion with Ag(I) and Au(I) salts to Fe(0) species, namely Fe(CO)5, Fe3(CO)12 and iron metal, involves the intermediate formation of several Ag-Fe and Au-Fe clusters, which may be selectively obtained by using substoichiometric molar ratios (comprised in the 0.33-1.75 range) between the reagents. On the basis of isolobal analogies, all the compounds which have been structurally characterized so far may be viewed as clusters of Group 11 elements stabilized by d8-Fe(CO)4 or bidentate Fe2(CO)8 ligands, in their several possible carbonyl stereochemistries. Rationalization of the miscellaneous steps of the above reactions enabled the synthesis of related heterometallic Cu-Ag and Au-Ag clusters. Their spectroscopic and structural behaviour are compared with those of previously reported Cu, Pd and Pt related compounds, as well as the corresponding Cu, Ag and Au cluster derivatives stabilized by d9-Co(CO)4 groups.

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Calderoni, F., Iapalucci, M.C., Longoni, G., Testoni, U. (1995). Silver and Gold Clusters Stabilized by Fe(CO)4 Ligands. In: Farrugia, L.J. (eds) The Synergy Between Dynamics and Reactivity at Clusters and Surfaces. NATO ASI Series, vol 465. Springer, Dordrecht. https://doi.org/10.1007/978-94-011-0133-2_22

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  • DOI: https://doi.org/10.1007/978-94-011-0133-2_22

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-94-010-4060-0

  • Online ISBN: 978-94-011-0133-2

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