Subcomponent flexibility enables conversion between D4-symmetric CdII8L8 and T-symmetric CdII4L4 assemblies

Jesús Mosquera, Tanya K. Ronson, Jonathan R. Nitschke

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

A flexible tris-formylpyridine subcomponent A was observed to produce three distinct products following CdII-templated self-assembly with different anilines. Two of the products were CdII4L4 tetrahedra, one with ligands puckered inward, and the other outward. The third product was a CdII8L8 structure having all mer stereochemistry, contrasting with the fac stereochemistry of the tetrahedra. These three complexes were observed to coexist in solution. The equilibrium between them could be influenced through guest binding and specific interactions between aniline subcomponents, allowing a selected one of the three to predominate under defined conditions.

Original languageEnglish
Pages (from-to)1812-1815
Number of pages4
JournalJournal of the American Chemical Society
Volume138
Issue number6
DOIs
Publication statusPublished - 27 Jan 2016

Keywords

  • self-assembly
  • stereochemistry
  • borromean rings
  • cadmium
  • aniline

Fingerprint Dive into the research topics of 'Subcomponent flexibility enables conversion between D<sub>4</sub>-symmetric Cd<sup>II</sup><sub>8</sub>L<sub>8</sub> and T-symmetric Cd<sup>II</sup><sub>4</sub>L<sub>4</sub> assemblies'. Together they form a unique fingerprint.

Cite this