4.7 Article

Selenacalix[3]triazines: synthesis and host-guest chemistry

Journal

CHEMICAL COMMUNICATIONS
Volume 48, Issue 1, Pages 43-45

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cc15473g

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Funding

  1. FWO
  2. KU Leuven
  3. Ministerie voor Wetenschapsbeleid
  4. Grants-in-Aid for Scientific Research [11F01760] Funding Source: KAKEN

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The heteracalixarene series (N/O/S) has been expanded with Se-bridged cyclotrimeric macrocycles. Selenacalix[3]triazines were synthesized by convenient one-pot nucleophilic aromatic substitution reactions and they showed peculiar supramolecular features. The N tridentate binding pocket was capable of coordinating both copper ions and anions.

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