Cargando…

Relating Design and Optoelectronic Properties of 1,4-Dihydropyrrolo[3,2-b]pyrroles Bearing Biphenyl Substituents

[Image: see text] Understanding the influence of peripheral functionality on optoelectronic properties of conjugated materials is an important task for the continued development of chromophores for myriad applications. Here, π-extended 1,4-dihydropyrrolo[3,2-b]pyrrole (DHPP) chromophores with varyin...

Descripción completa

Detalles Bibliográficos
Autores principales: Hawks, Allison M., Altman, Drake, Faddis, Ryan, Wagner, Ethan M., Bell, Kenneth-John J., Charland-Martin, Ariane, Collier, Graham S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461294/
https://www.ncbi.nlm.nih.gov/pubmed/37561612
http://dx.doi.org/10.1021/acs.jpcb.3c03061
_version_ 1785097819012464640
author Hawks, Allison M.
Altman, Drake
Faddis, Ryan
Wagner, Ethan M.
Bell, Kenneth-John J.
Charland-Martin, Ariane
Collier, Graham S.
author_facet Hawks, Allison M.
Altman, Drake
Faddis, Ryan
Wagner, Ethan M.
Bell, Kenneth-John J.
Charland-Martin, Ariane
Collier, Graham S.
author_sort Hawks, Allison M.
collection PubMed
description [Image: see text] Understanding the influence of peripheral functionality on optoelectronic properties of conjugated materials is an important task for the continued development of chromophores for myriad applications. Here, π-extended 1,4-dihydropyrrolo[3,2-b]pyrrole (DHPP) chromophores with varying electron-donating or electron-withdrawing capabilities were synthesized via Suzuki cross-coupling reactions, and the influence of functionality on optoelectronic properties was elucidated. First, chromophores display distinct differences in the UV–vis absorbance spectra measured via UV–vis absorbance spectroscopy in addition to changes in the onset of oxidation measured with cyclic voltammetry and differential pulse voltammetry. Solution oxidation studies found that variations in the electron-donating and -withdrawing capabilities result in different absorbance profiles of the radical cations that correspond to quantifiably different colors. In addition to fundamental insights into the molecular design of DHPP chromophores and their optoelectronic properties, two chromophores display high-contrast electrochromism, which makes them potentially compelling in electronic devices. Overall, this study represents the ability to fine-tune the optoelectronic properties of DHPP chromophores in their neutral and oxidized states and expands the understanding of structure–property relationships that will guide the continued development of DHPP-based materials.
format Online
Article
Text
id pubmed-10461294
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Chemical Society
record_format MEDLINE/PubMed
spelling pubmed-104612942023-08-29 Relating Design and Optoelectronic Properties of 1,4-Dihydropyrrolo[3,2-b]pyrroles Bearing Biphenyl Substituents Hawks, Allison M. Altman, Drake Faddis, Ryan Wagner, Ethan M. Bell, Kenneth-John J. Charland-Martin, Ariane Collier, Graham S. J Phys Chem B [Image: see text] Understanding the influence of peripheral functionality on optoelectronic properties of conjugated materials is an important task for the continued development of chromophores for myriad applications. Here, π-extended 1,4-dihydropyrrolo[3,2-b]pyrrole (DHPP) chromophores with varying electron-donating or electron-withdrawing capabilities were synthesized via Suzuki cross-coupling reactions, and the influence of functionality on optoelectronic properties was elucidated. First, chromophores display distinct differences in the UV–vis absorbance spectra measured via UV–vis absorbance spectroscopy in addition to changes in the onset of oxidation measured with cyclic voltammetry and differential pulse voltammetry. Solution oxidation studies found that variations in the electron-donating and -withdrawing capabilities result in different absorbance profiles of the radical cations that correspond to quantifiably different colors. In addition to fundamental insights into the molecular design of DHPP chromophores and their optoelectronic properties, two chromophores display high-contrast electrochromism, which makes them potentially compelling in electronic devices. Overall, this study represents the ability to fine-tune the optoelectronic properties of DHPP chromophores in their neutral and oxidized states and expands the understanding of structure–property relationships that will guide the continued development of DHPP-based materials. American Chemical Society 2023-08-10 /pmc/articles/PMC10461294/ /pubmed/37561612 http://dx.doi.org/10.1021/acs.jpcb.3c03061 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Hawks, Allison M.
Altman, Drake
Faddis, Ryan
Wagner, Ethan M.
Bell, Kenneth-John J.
Charland-Martin, Ariane
Collier, Graham S.
Relating Design and Optoelectronic Properties of 1,4-Dihydropyrrolo[3,2-b]pyrroles Bearing Biphenyl Substituents
title Relating Design and Optoelectronic Properties of 1,4-Dihydropyrrolo[3,2-b]pyrroles Bearing Biphenyl Substituents
title_full Relating Design and Optoelectronic Properties of 1,4-Dihydropyrrolo[3,2-b]pyrroles Bearing Biphenyl Substituents
title_fullStr Relating Design and Optoelectronic Properties of 1,4-Dihydropyrrolo[3,2-b]pyrroles Bearing Biphenyl Substituents
title_full_unstemmed Relating Design and Optoelectronic Properties of 1,4-Dihydropyrrolo[3,2-b]pyrroles Bearing Biphenyl Substituents
title_short Relating Design and Optoelectronic Properties of 1,4-Dihydropyrrolo[3,2-b]pyrroles Bearing Biphenyl Substituents
title_sort relating design and optoelectronic properties of 1,4-dihydropyrrolo[3,2-b]pyrroles bearing biphenyl substituents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10461294/
https://www.ncbi.nlm.nih.gov/pubmed/37561612
http://dx.doi.org/10.1021/acs.jpcb.3c03061
work_keys_str_mv AT hawksallisonm relatingdesignandoptoelectronicpropertiesof14dihydropyrrolo32bpyrrolesbearingbiphenylsubstituents
AT altmandrake relatingdesignandoptoelectronicpropertiesof14dihydropyrrolo32bpyrrolesbearingbiphenylsubstituents
AT faddisryan relatingdesignandoptoelectronicpropertiesof14dihydropyrrolo32bpyrrolesbearingbiphenylsubstituents
AT wagnerethanm relatingdesignandoptoelectronicpropertiesof14dihydropyrrolo32bpyrrolesbearingbiphenylsubstituents
AT bellkennethjohnj relatingdesignandoptoelectronicpropertiesof14dihydropyrrolo32bpyrrolesbearingbiphenylsubstituents
AT charlandmartinariane relatingdesignandoptoelectronicpropertiesof14dihydropyrrolo32bpyrrolesbearingbiphenylsubstituents
AT colliergrahams relatingdesignandoptoelectronicpropertiesof14dihydropyrrolo32bpyrrolesbearingbiphenylsubstituents