Abstract
The reaction of the [Rh7(CO)16]3- cluster anion with Ge2+ salts, in different stoichiometric ratios and under different atmospheres, leads to the formation of new heterometallic Rh-Ge clusters, representing the first known examples of Rh carbonyl compounds containing interstitial germanium atoms. More specifically, under N2 the reaction progressively affords the new [Rh13Ge(CO)25]3- and [Rh14Ge2(CO)30]2- clusters in good yields, with the Ge atoms located in cubic and square-anti-prismatic cavities, respectively. However, under a CO atmosphere, the [Rh13Ge(CO)25]3- derivative undergoes a significant structural and chemical rearrangement giving the new compound, [Rh12Ge(CO)27]4-, where Ge is hosted in an icosahedral metal cage. All species have been characterized by IR spectroscopy and ESI mass spectrometry, and their structures have been elucidated by single-crystal X-ray diffraction. Additionally, preliminary biological tests on the [Rh13Ge(CO)25]3- and [Rh14Ge2(CO)30]2- clusters show that they are cytotoxic to various cell lines.
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