Six states switching of redox-active molecular tweezers by three orthogonal stimuli

Author

Doistau, Benjamin

Benda, Lorien

Cantin, Jean-Louis

Chamoreau, Lise-Marie

Ruiz Sabín, Eliseo

Marvaud, Valerie

Hasenknopf, Bernold

Vives, Guillaume

Publication date

2020-04-01T10:22:10Z

2020-04-01T10:22:10Z

2017-07-12

2020-04-01T10:22:10Z

Abstract

A six level molecular switch based on terpyridine(Ni-salphen)(2) tweezers and addressable by three orthogonal stimuli (metal coordination, redox reaction, and guest binding) is reported. By a metal coordination stimulus, the tweezers can be mechanically switched from an open 'W'-shaped conformation to a closed 'U'-shaped form. Theses two states can each be reversibly oxidized by the redox stimulus and bind to a pyrazine guest resulting in four additional states. All six states are stable and accessible by the right combination of stimuli and were studied by NMR, XRD, EPR spectroscopy, and DFT calculations. The combination of the supramolecular concepts of mechanical motion and guest binding with the redox noninnocent and valence tautomerism properties of Ni-salphen complexes added two new dimensions to a mechanical switch.

Document Type

Article
Accepted version

Language

English

Subjects and keywords

Lligands; Radicals (Química); Oxidoreductases; Glucosa; Ligands; Radicals (Chemistry); Oxidoreductases; Glucose

Publisher

American Chemical Society

Related items

Versió postprint del document publicat a: https://doi.org/10.1021/jacs.7b02945

Journal of the American Chemical Society, 2017, vol. 139, num. 27, p. 9213-9220

https://doi.org/10.1021/jacs.7b02945

Rights

(c) American Chemical Society , 2017

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