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Issue 33, 2015
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Redox-dependent self-sorting toggles a rotary nanoswitch

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Abstract

The pyridine–pyrimidine (py–pym) arm as the moving part of the two-state nanomechanical rotary switch [Cu(1)]+ is toggled reversibly between two stations using one-electron oxidation/reduction. In state I, the arm is attached via Cu+ complexation to a sterically encumbered phenanthroline and in state II to a zinc porphyrin station. Toggling is realised by charging and discharging an external input signal, the ferrocene-appended diimine ligand 2. Addition of 2 leads to formation of the intermolecular complex [Cu(1)(2)]+ paralleled by a move of the py–pym arm to the zinc porphyrin station. Upon oxidation at the ferrocenyl unit, 2+ detaches from [Cu(1)(2)]2+ so that [Cu(1)]+ is formed in state I. Switching was ascertained by NMR, UV-Vis spectroscopy and cyclic voltammetry.

Graphical abstract: Redox-dependent self-sorting toggles a rotary nanoswitch

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Supplementary files

Article information


Submitted
22 May 2015
Accepted
14 Jul 2015
First published
27 Jul 2015

Org. Biomol. Chem., 2015,13, 8937-8944
Article type
Paper

Redox-dependent self-sorting toggles a rotary nanoswitch

M. Schmittel, S. De and S. Pramanik, Org. Biomol. Chem., 2015, 13, 8937
DOI: 10.1039/C5OB01041A

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