[M@Sn14-xSbx]q- (M = La, Ce, or U; x = 6-8; q = 3, 4): Interaction of 4f or 5f Metal Ions with 5p Metal Atoms in Intermetalloid Clusters.

The impact of 4f metal ions Ln3+ (Ln = La or Ce) versus 5f metal ions Un+ (n = 3 or 4) on the compositions and distribution of 5p metal atoms in the cluster shells of endohedral species [M@Sn14-xSbx]q- (M = La, Ce, or U; x = 6-8; q = 3, 4) was studied by means of combined experimental and quantum chemical investigations. While all known f-block metal ion-centered endohedral clusters possessed combinations of larger main group metal atoms so far (Sn/Bi or Pb/Bi), resulting in mixtures of 13- and 14-atom cages, the 14-atom cages reported herein comprise exclusively Sn and Sb atoms and therefore are challenged in accommodating the large 4f and 5f ions. We show that the clusters form in reactions of (Sn2Sb2)2- anions with [Ln(C5Me4H)3] or [U(C5Me4H)3Cl], and that salts of [La@Sn6Sb8]3-, [La@Sn7Sb7]4-, [U@Sn8Sb6]4-, and [U@Sn7Sb7]3- can be isolated from them. The assignment of Sn versus Sb in the encapsulating cage follows a simple rule. Different central atoms cause only slight differences in this regard and with respect to distortions of the cluster shells. The reactions also yielded the salt of the new binary anion (Sn4Sb4)2- that was recently predicted by quantum chemical studies.

Between Elemental Match and Mismatch: From K12 Ge3.5 Sb6 to Salts of (Ge2 Sb2 )2- , (Ge4 Sb12 )4- , and (Ge4 Sb14 )4.

The solid mixture "K2 GeSb" was shown to comprise single-crystalline K12 Ge3.5 Sb6 (1), a double salt of K5 [GeSb3 ] with carbonate-like [GeSb3 ]5- anions, and the metallic Zintl phase K2 Ge1.5 . Extraction of 1 with ethane-1,2-diamine in the presence of crypt-222 afforded [K(crypt-222)]+ salts of several novel binary Zintl anions: (Ge2 Sb2 )2- (in 2), (Ge4 Sb12 )4- (in 3), and in the presence of [AuMePPh3 ] also (Ge4 Sb14 )4- (in 4). The anion in 2 represents a predicted, yet heretofore missing pseudo-tetrahedral anion. 4 comprises a cluster analogous to (Ge4 Bi14 )4- and (Ga2 Bi16 )4- , and thus one of the most Sb-rich binary p-block anions. The unprecedented cluster topology in 3 can be viewed as a defect-version of the one in 4 upon following a "dead end" of cluster growth. The findings indicate that Ge and Sb atoms are at the border of a well-matching and a mismatch elemental combination. We discuss the syntheses, the geometric structures, and the electronic structures of the new compounds.

High-Spin Imido Cobalt Complexes with Imidyl Radical Character*.

We report on the synthesis of a variety of trigonal imido cobalt complexes [Co(NAryl)L2 ]- , (L=N(Dipp)SiMe3 ), Dipp=2,6-diisopropylphenyl) with very long Co-NAryl bonds of around 1.75 Å. Their electronic structure was interrogated using a variety of physical and spectroscopic methods such as EPR or X-Ray absorption spectroscopy which leads to their description as highly unusual imidyl cobalt complexes. Computational analyses corroborate these findings and further reveal that the high-spin state is responsible for the imidyl character. Exchange of the Dipp substituent on the imide by the smaller mesityl function (2,4,6-trimethylphenyl) effectuates the unexpected Me3 Si shift from the ancillary ligand set to the imidyl nitrogen, revealing a highly reactive, nucleophilic character of the imidyl unit.

Insight into the formation of bismuth-tungsten carbonyl clusters.

Multimetallic clusters play a key role as models to doped metals, as candidates to new types of superatomic catalysts and as precursors to new multimetallic solids. Understanding formation pathways is an essential and necessary step forward in the development of cluster synthesis and research, yet remains considerably lacking owing to difficulty in identification of intermediates and the ill-defined nature of common starting materials. Here we show progress in this regard by investigating the reactivity of an intermetallic solid of nominal composition 'K5Ga2Bi4' with [W(cod)(CO)4] upon extraction with ethane-1,2-diamine (en) and 4,7,13,16,21,24-hexaoxa-1,10-diazabicyclo[8.8.8]hexacosane (crypt-222). Several polybismuthide intermediates and by-products were identified along the reaction pathway, ultimately forming the new polybismuthide salt [K(crypt-222)]3[µ:η3-Bi3{W(CO)3}2]∙en∙tol. DFT calculations revealed plausible reaction schemes for the transformations taking place in the reaction mixture providing insight into the complex reactivity of 'K5Ga2Bi4' on the basis of in situ generation of Bi22-.