Abstract
We report on the design, synthesis, and operation of a bimetallic molecular biped on a three-foothold track. The "walker" features a palladium(11) complex "foot" that can be selectively stepped between 4-dimethylaminopyridine and pyridine ligand sites on the track via reversible protonation while the walker remains attached to the track throughout by means of a kinetically inert platinum(11) complex foot. The substitution pattern of the three ligand binding sites, together with the kinetic stability of the metal ligand coordination bonds, affords the two positional isomers a high degree of metastability, meaning that altering the chemical state of the track does not automatically instigate stepping in the absence of an additional stimulus (heat in the presence of a coordinating solvent). The use of metastable metal complexes for foot track interactions offers a promising alternative to dynamic covalent chemistry for the design of small-molecule synthetic molecular walkers.
Original language | English |
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Pages (from-to) | 2094-2100 |
Number of pages | 7 |
Journal | Journal of the American Chemical Society |
Volume | 136 |
Issue number | 5 |
Early online date | 14 Jan 2014 |
DOIs | |
Publication status | Published - 5 Feb 2014 |
Keywords
- Synthetic Small-Molecule
- Different Coordinating Units
- Redox-Active Ligand
- Machine Prototypes
- Transition-Metal
- Information Ratchet
- Ring
- Copper
- Rotaxane
- Motion