4.8 Article

An Electrochemically and Thermally Switchable Donor-Acceptor [c2]Daisy Chain Rotaxane

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 53, Issue 7, Pages 1953-1958

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201308498

Keywords

cyclic voltammetry; donor-acceptor systems; molecular dynamics; molecular recognition; rotaxanes

Funding

  1. Non-Equilibrium Energy Research Center (NERC), an Energy Frontiers Research Center (EFRC)
  2. US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-SC0000989]
  3. Northwestern University (NU) [34-494]
  4. Office of Naval Research (ONR) [N00014-13-1-0058]
  5. International Institute for Nanotechnology (IIN) at Northwestern University (NU)

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Although motor proteins are essential cellular components that carry out biological processes by converting chemical energy into mechanical motion, their functions have been difficult to mimic in artificial synthetic systems. Daisy chains are a class of rotaxanes which have been targeted to serve as artificial molecular machines because their mechanically interlocked architectures enable them to contract and expand linearly, in a manner that is reminiscent of the sarcomeres of muscle tissue. The scope of external stimuli that can be used to control the musclelike motions of daisy chains remains limited, however, because of the narrow range of supramolecular motifs that have been utilized in their templated synthesis. Reported herein is a cyclic daisy chain dimer based on -associated donor-acceptor interactions, which can be actuated with either thermal or electrochemical stimuli. Molecular dynamics simulations have shown the daisy chain's mechanism of extension/contraction in the ground state in atomistic detail.

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