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

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...

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Detalles Bibliográficos
Autores principales: Broløs, Line, Nielsen, Mogens Brøndsted
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052312/
https://www.ncbi.nlm.nih.gov/pubmed/35495470
http://dx.doi.org/10.1039/d0ra02787a
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author Broløs, Line
Nielsen, Mogens Brøndsted
author_facet Broløs, Line
Nielsen, Mogens Brøndsted
author_sort Broløs, Line
collection PubMed
description 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.
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spelling pubmed-90523122022-04-29 Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems Broløs, Line Nielsen, Mogens Brøndsted RSC Adv Chemistry 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. The Royal Society of Chemistry 2020-04-16 /pmc/articles/PMC9052312/ /pubmed/35495470 http://dx.doi.org/10.1039/d0ra02787a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Broløs, Line
Nielsen, Mogens Brøndsted
Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems
title Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems
title_full Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems
title_fullStr Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems
title_full_unstemmed Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems
title_short Dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems
title_sort dimers of pyrrolo-annelated indenofluorene-extended tetrathiafulvalenes – large multiredox systems
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052312/
https://www.ncbi.nlm.nih.gov/pubmed/35495470
http://dx.doi.org/10.1039/d0ra02787a
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