The synthesis and single-crystal X-ray diffraction structure of a dimeric zinc-seamed nanocapsule using a mixed pyrogallol/resorcinol[4]arene are presented. The use of "mixed" macrocycles results in an incomplete seam of coordination bonds around the nanocapsule's typically octa-metalated belt. The self-assembly of the nanocapsule occurs such that the single resorcinol moiety of each macrocycle aligns transversely. This yields a hepta-metalated capsule where the defect occurs in such a way as to provide minimal disruption to the overall structure of the nanocapsule.
C-alkylpyrogallol[4]arenes (PgCs) have been studied for their ability to form metal-organic nanocapsules (MONCs) through coordination to appropriate metal ions. Here we present the synthesis and characterization of an MnII/MnIII-seamed MONC in addition to its electrochemical and magnetic behavior. This MONC assembles from 24 manganese ions and 6 PgCs, while an additional metal ion is located on the capsule interior, anchored through the introduction of bridging nitrite ions. The latter originate from an in situ redox reaction that occurs during the self-assembly process, thus representing a new route to otherwise unobtainable nanocapsules.
The synthesis and X-ray crystallographic
structure of the first
cobalt-seamed hexameric nanocapsule, [Co24(C-pentylpyrogallol[4]arene)6], is presented. The overall
metal–ligand arrangement of this novel capsule is similar to
that of previously reported copper- and nickel-seamed hexameric nanocapsules.
However, the title nanocapsule encloses a larger void space than those
found in previous hexameric nanocapsules.
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