1,3-ALTERNATE-THIACALIX[4]ARENE-BASED DIMER: SYNTHESIS AND INCLUSION BEHAVIOR

Synthetic approaches to flexible and adaptable thiacalix[4]arene dimer, in which the thiacalix[4]arene units constrain 1,3-alternate conformation, by molecular assembly are presented. The thiacalix[4]arene dimer shows high affinity toward Cs⁺ and K⁺ ions. Encapsulation of Cs⁺ by the internal cavity of the dimer strongly suggests that the size match factor drives the process. On the other hand, the K⁺ is encapsulated by the thiacalix[4]arenes units by supramolecular interaction (cation-π).

Keywords:

• Dimer
• Molecular recognition
• Thiacalix[4]arene