“…[18] Such ligand-free multimetallic anions belong to the family of Zintl clusters that can be accessed by reacting homo-or heteroatomic p-block metal anions with d-block or f-block metal compounds. [7] In this context, reactions of x [K(crypt-222)] 2 (Sn 2 Sb 2 )•en with y [AuMePPh 3 ]w ere reported to yield [K(crypt-222)] 3 -[(Sn 2 Sb 2 ) 2 Au]( A) [19,20] in en (x:y = 2:1) or [K(crypt-222)] 4 -[(Sn 5 Sb 3 Au) 2 ]•2 py (B) [18] in pyridine (x:y = 1:2) (crypt-222 = 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]-hexacosane, en = ethane-1,2-diamine;p y = pyridine), yet the underlying reactions are only poorly understood. Thef ormation of the anion in A,[{(Sn 2 Sb 2 ) 2À } 2 Au + ] 3À ,atfirst glance shows no sign of redox chemistry in comparison with the reactants.H owever,t he anion in B,[ {(Sn 5 Sb 3 ) 3À Au + } 2 ] 4À ,i so verall oxidized relative to the (Sn 2 Sb 2 ) 2À anion-and in both cases,t he gold complex apparently released not only the PPh 3 groups,b ut also the (CH 3 ) À ligands.F or this,i ti sv ery obvious that side reactions take place that have not yet been elucidated.…”