Abstract
Two switchable, palindromically constituted bistable [3]rotaxanes have been designed and synthesized with a pair of mechanically mobile rings encircling a single dumbbell. These designs are reminiscent of a "molecular muscle" for the purposes of amplifying and harnessing molecular mechanical motions. The location of the two cyclobis(paraquat-p-phenylene) (CBPQT(4+)) rings can be controlled to be on either tetrathiafulvalene (TTF) or naphthalene (NP) stations, either chemically ((1)H NMR spectroscopy) or electrochemically (cyclic voltammetry), such that switching of inter-ring distances from 4.2 to 1.4 nm mimics the contraction and extension of skeletal muscle, albeit on a shorter length scale. Fast scan-rate…
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Authors
15Topics & keywords
Topics
Keywords
- Rotaxane
- Chemistry
- Monolayer
- Cyclic voltammetry
- Bistability
- Dumbbell
- Molecular switch
- Tetrathiafulvalene
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Funding
- NSNational Science FoundationAwards: 0103559, 0092036, 9974928
- NANational Aeronautics and Space Administration
- SNSchweizerischer Nationalfonds zur Förderung der Wissenschaftlichen ForschungAwards: 21-03, 10355, 103559
- DADefense Advanced Research Projects Agency
- ARAdvanced Research Projects Agency
- DODivision of Chemistry