Abstract
A radical interaction has been employed as the recognition motif in the template-directed synthesis of a [2]rotaxane composed of cyclobis(paraquat-p- phenylene) and a viologen derivative. The ruthenium tris(bipyridine)/ triethanolamine system is used as the electron-transfer photocatalyst to generate the necessary radical cation components that result in the formation of an inclusion complex. A stoppering reaction follows to form the mechanical bond.
Original language | English (US) |
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Pages (from-to) | 8260-8265 |
Number of pages | 6 |
Journal | Angewandte Chemie - International Edition |
Volume | 49 |
Issue number | 44 |
DOIs | |
State | Published - Oct 25 2010 |
Keywords
- Electrochemistry
- Radical dimerization
- Rotaxanes
- Self-assembly
- Template-directed synthesis
ASJC Scopus subject areas
- Catalysis
- General Chemistry