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10.1002/open.201402073

http://scihub22266oqcxt.onion/10.1002/open.201402073
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C4380948!4380948!25861565
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suck abstract from ncbi


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pmid25861565      ChemistryOpen 2015 ; 4 (1): 18-21
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  • Reversible Mechanical Switching of Magnetic Interactions in a Molecular Shuttle #MMPMID25861565
  • Bleve V; Schäfer C; Franchi P; Silvi S; Mezzina E; Credi A; Lucarini M
  • ChemistryOpen 2015[Feb]; 4 (1): 18-21 PMID25861565show ga
  • An acid?base switchable molecular shuttle based on a [2]rotaxane, incorporating stable radical units in both the ring and dumbbell components, is reported. The [2]rotaxane comprises a dibenzo[24]crown-8 ring (DB24C8) interlocked with a dumbbell component that possesses a dialkylammonium (NH2+) and a 4,4?-bipyridinium (BPY2+) recognition site. Deprotonation of the rotaxane NH2+ centers effects a quantitative displacement of the DB24C8 macroring to the BPY2+ recognition site, a process that can be reversed by acid treatment. Interaction between stable 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) radicals connected to the ring and dumbbell components could be switched between noncoupled (three-line electron paramagnetic resonance (EPR) spectrum) and coupled (five-line EPR spectrum) upon displacement of the spin-labelled DB24C8 macroring. The complete base- and acid-induced switching cycle of the EPR pattern was repeated six times without an appreciable loss of signal, highlighting the reversibility of the process. Hence, this molecular machine is capable of switching on/off magnetic interactions by chemically driven reversible mechanical effects. A system of this kind represents an initial step towards a new generation of nanoscale magnetic switches that may be of interest for a variety of applications.
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