The reaction of [ReBr3(CO)3][NEt4]2 with 3‐hydroxy‐1,2,3‐benzotriazine‐4(3H)‐one in the presence of base gave the ionic rhenium complex [ReBr(C7H4N3O2)(CO)3][NEt4] (2) which was crystallographically characterized. A neutral metallamacrocycle 3 was obtained upon abstraction of [NEt4]Br from complex 2. This complex cocrystallizes with an unusual C3‐symmetric [Ag(η2‐benzene)3(OH2)][BF4] complex as evidenced by single‐crystal X‐ray diffraction. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

A coordination cage with an elusive icosahedral geometry was obtained by K+-induced rearrangement of a hexanuclear [(cymene)Ru(pyridine-3,5-dicarboxylate)]6 complex.

The reaction of [(Et(3)P)PdCl(2)](2) with 2,3-dihydroxypyridine, 5-chloro-2,3,-dihydroxypyridine, or 2-hydroxynicotinic acid in the presence of base gives neutral, metallomacrocyclic compounds in which the heterocycles act as dianionic, bridging ligands. The macrocycles contain four or ten palladium atoms as evidenced by single crystal X-ray analyses.

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