Issue 61, 2015

Diindenothienoacene–tetrathiafulvalene redox systems

Abstract

Extended tetrathiafulvalenes with central diindenothienoacene cores were prepared and studied for their redox and spectroelectrochemical properties, which depended strongly on the orientation of the thiophene rings. The cations undergo remarkably strong associations, rendering them attractive as redox-controllable tectons in supramolecular chemistry, and in one case crystals were grown by electrocrystallization.

Graphical abstract: Diindenothienoacene–tetrathiafulvalene redox systems

Supplementary files

Article information

Article type
Communication
Submitted
30 Apr 2015
Accepted
28 May 2015
First published
28 May 2015

RSC Adv., 2015,5, 49748-49751

Diindenothienoacene–tetrathiafulvalene redox systems

M. A. Christensen, G. E. Rudebusch, C. R. Parker, C. L. Andersen, A. Kadziola, M. M. Haley, O. Hammerich and M. B. Nielsen, RSC Adv., 2015, 5, 49748 DOI: 10.1039/C5RA09581F

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