Issue 26, 2020

Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems

Abstract

Novel scaffolds of indenofluorene (IF)-extended tetrathiafulvalenes (TTF) were synthesized starting from a new pyrrolo-annelated IF-TTF monomer. Rigid para- and meta-phenylene linked dimers were obtained via N-arylation reactions of the monomer, and their optical and redox properties were elucidated by UV-Vis absorption spectroscopy and cyclic and differential pulse voltammetries.

Graphical abstract: Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems

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Article information

Article type
Paper
Submitted
03 Mar 2020
Accepted
31 Mar 2020
First published
16 Apr 2020
This article is Open Access
Creative Commons BY license

RSC Adv., 2020,10, 15030-15033

Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems

L. Broløs and M. B. Nielsen, RSC Adv., 2020, 10, 15030 DOI: 10.1039/D0RA02787A

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