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Femtosecond pump-probe absorption spectroscopy in tetrahydrofuran solution has been used to investigate the dynamics of a metalloid cluster compound {Ge9[Si(SiMe3)3]3}(-). Upon UV photoexcitation, the transients in the near-infrared spectral region showed signatures reminiscent of excess electrons in THF (bound or quasi-free) whereas in the visible part excited state dynamics of the cluster complex dominates.

Reductions of the β-diketiminato group 14 metal(II) chloride complexes, [((But)MesNacnac)ECl] ((But)MesNacnac = [(MesNCBu(t))(2)CH](-); Mes = mesityl; E = Ge, Sn or Pb), with a magnesium(I) dimer have led to differing outcomes, which include the formation of the first β-diketiminato group 14 metal(I) dimer, [{((But)MesNacnac)Sn}(2)]., (This journal is © The Royal Society of Chemistry 2012)

The reactions of the metalloid cluster {Ge9[Si(SiMe3)3]3}- with Cr(CO)5COE (COE=cyclooctene) and Cr(CO)3(CH3CN)3 lead to the new cluster compounds {Ge9[Si(SiMe3)3]3Cr(CO)5}- and {Ge9[Si(SiMe3)3]3Cr(CO)3}-, whose structural and electronic properties are presented.

The reaction of GeBr with LiGe(SiMe(3))(3) yields the largest metalloid cluster compound of germanium Ge(14)[Ge(SiMe(3))(3)](5)Li(3)(THF)(6), in which 14 germanium atoms are arranged as a hollow sphere in the cluster core, showing that in the case of germanium also fullerene-like compounds might be present in the borderland between the molecular and solid states.