Abstract
A molecular system comprising a cationic zinc complex and an amino acid-derived ambident ligand having phosphate and carboxylate binding sites undergoes a series of rearrangements in which the metal cation migrates autonomously from one site to another. The location of the metal is identified by the circular dichroism spectrum of a ligated bis(2-quinolylmethyl)-(2-pyridylmethyl)amine (BQPA) chromophore, which takes a characteristic shape at each binding site. Migration is fuelled by the decomposition of trichloroacetic acid to CO2 and CHCl3, which progressively neutralises the acidity of the system as a function of time, revealing in sequence binding sites of increasing basicity. The migration rate responds to control by variation of the temperature, water content and triethylamine concentration, while an excess of fuel controls the duration of an induction period before the migration event.
| Original language | English |
|---|---|
| Article number | e202202247 |
| Journal | Chemistry - A European Journal |
| Volume | 28 |
| Issue number | 59 |
| Early online date | 17 Aug 2022 |
| DOIs | |
| Publication status | Published - 21 Oct 2022 |
Bibliographical note
Funding Information:This work was supported by the EPSRC (Programme Grant ‘Molecular Robotics’ EP/P027067), the ERC (Advanced Grant DOGMATRON 883786), and the EU through the European Regional Development Fund project TK141 (2014‐2020.4.01.15‐0011).
Publisher Copyright:
© 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH.
Research Groups and Themes
- Organic & Biological
Keywords
- chemical fuel
- circular dichroism
- host-guest systems
- metal complexes
- molecular automata