Organo-Zintl clusters soluble in conventional organic solvents: setting the stage for organo-Zintl cluster chemistry.

نویسندگان

  • Michael W Hull
  • Slavi C Sevov
چکیده

Organo-Zintl cluster ions were synthesized by reactions of alkynes with Ge94- clusters in ethylenediamine. The triple bonds are hydrogenated to double bonds during the process. The resulting dial-kenylated species [RHC=CHGe9CH=CHR]2- have lower charge, their alkali-metal cations can be exchanged for tetralkylammonium cations, and the resulting compounds are soluble in nonpolar solvents. This was demonstrated with [H2C=CHGe9CH=CH2]2-, which was structurally characterized with [K-(18-crown-6)]+, [Me4N]+, and [Pr4N]+ as countercations. The solubility of its salt with [Oc4N]+ in various conventional organic solvents was studied.

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عنوان ژورنال:
  • Inorganic chemistry

دوره 46 26  شماره 

صفحات  -

تاریخ انتشار 2007