Abstract
A benzyl substituted 4-pyrrolidinopyridinium salt (G) with multiple active sites including benzyl, pyridinium and pyrrole groups has been synthesized. The interaction between G and a series of cucurbit[n]urils (TMeQ[6], Q[7], Q[8], Q[10]), has been studied both in aqueous solution and in the solid state. The binding interaction site between G and the Q[n] can be controlled by the size of the cavity of the Q[n]s. In the case of TMeQ[6], the benzyl is accommodated within the cavity, whilst for Q[7] and Q[8], the pyrrole ring and the benzyl are accommodated within the cavity of the Q[7/8], and the latter can shuttle on the guest G in a state of dynamic equilibrium. For the larger cavity of Q[10], the entire G molecule is located within the cavity of the Q[10].
| Original language | English |
|---|---|
| Pages (from-to) | 4311-4318 |
| Number of pages | 8 |
| Journal | New Journal of Chemistry |
| Volume | 44 |
| Issue number | 11 |
| Early online date | 20 Feb 2020 |
| DOIs | |
| Publication status | Published - 21 Mar 2020 |
ASJC Scopus subject areas
- Catalysis
- General Chemistry
- Materials Chemistry