Reactions of the bicyclic silicon(I) ring compound [Si 4 {N(SiMe 3 )Dipp} 4 ] 1 with the chalcogens O 2 , Se, Te and the group 16 element compounds TeP(nBu) 3 and Me 3 NO afforded unprecedented amido-substituted cage compounds such as [Si 4 Se 3 {N(SiMe 3 )Dipp} 4 ] 3-5 with two different tricyclo-heptane-[a]type cages and one with a defect-hetero-cubane-type Si 4 Se 3 core, and [Si 4 Te 6 {N(SiMe 3 )Dipp} 4 ] 6 with an adamantane-type cage. These compounds were examined by single-crystal X-ray diffraction, multinuclear NMR spectroscopy in solution, ESI mass spectrometry, UV/Vis spectroscopy, and DFT calculations.Si 4 Se 6 (Thex) 4 (Thex = 1,1,2-trimethylpropyl) is known with type II and type III cores. [11,12] In general, compounds with type II core can be converted to compounds with type III topology under thermal treatment. [11,12] By contrast, silicon tellurium compounds decorated by organic substituents are rare. Only the silatellurane with type III structural motif Si 4 (CH 2 ) 2 Te 4 Me 4 ·CDCl 3 was described with two methylene groups and four Te atoms at the two-coordinate positions in the adamantane-type cage (III) synthesized by the reaction of the disilylmethane CH 2 (SiMeCl 2 ) 2 with Li 2 Te. [13] In general, cage compounds with Si-Te bonds are scarce due to the high sensitivity of these compounds towards air and moisture. [14] Eur.