Tuning the Electronic Properties of Bridged Dithienyl‐, Difuryl‐, Dipyrrolyl‐Vinylene as Precursors of Small‐Bandgap Conjugated Polymer.

Optoelectronic properties of linear π-conjugated polymers/oligomers are of great importance for the fabrication of organic photonic and electronic devices. To this end, the π-conjugated polymers/oligomers need to meet both optoelectronic and key structural properties in order to fulfill their implementation as active components. In particular, they need to possess low bandgap and high thermal, conformational, and photochemical stabilities. So far, several strategies have been developed to attain such requirements including the covalent and non-covalent rigidification concepts of the π-conjugated systems. On the basis of these findings, we describe herein the theoretical studies of novel series of covalently bridged derivatives demonstrating the benefits of the strategy. Comparison of these derivatives with compounds previously described in the literature highlights enhanced optoelectronic properties and behaviors that would be beneficial for the construction and development of new linear π-conjugated polymers.

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Publication Details

Journal
Chemistry - A European Journal
Published
2024-08-13
DOI
https://doi.org/10.1002/chem.202402461
Citations
2
Primary Topic
Organic Electronics and Photovoltaics
Type
article
Field-Weighted Citation Impact
0.42

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article

Tuning the Electronic Properties of Bridged Dithienyl‐, Difuryl‐, Dipyrrolyl‐Vinylene as Precursors of Small‐Bandgap Conjugated Polymer.

Tommaso Nicolini, Jean‐Marc Sotiropoulos, Jean‐Manuel Raimundo, Jordan Garo
2 citations
Chemistry - A European Journal
Organic Electronics and Photovoltaics
0.42
article

Tuning the Electronic Properties of Bridged Dithienyl‐, Difuryl‐, Dipyrrolyl‐Vinylene as Precursors of Small‐Bandgap Conjugated Polymer.

Tommaso Nicolini, Jean‐Marc Sotiropoulos, Jean‐Manuel Raimundo, Jordan Garo
article en
2 citations

Abstract

Optoelectronic properties of linear π-conjugated polymers/oligomers are of great importance for the fabrication of organic photonic and electronic devices. To this end, the π-conjugated polymers/oligomers need to meet both optoelectronic and key structural properties in order to fulfill their implementation as active components. In particular, they need to possess low bandgap and high thermal, conformational, and photochemical stabilities. So far, several strategies have been developed to attain such requirements including the covalent and non-covalent rigidification concepts of the π-conjugated systems. On the basis of these findings, we describe herein the theoretical studies of novel series of covalently bridged derivatives demonstrating the benefits of the strategy. Comparison of these derivatives with compounds previously described in the literature highlights enhanced optoelectronic properties and behaviors that would be beneficial for the construction and development of new linear π-conjugated polymers.

Chemistry - A European JournalVol. 30(57)
Centre National de la Recherche Scientifique (FR), Université de Pau et des Pays de l'Adour (FR), Aix-Marseille Université (FR), Institut des Sciences Analytiques et de Physico-Chimie pour l'Environnement et les Matériaux (FR), Centre Interdisciplinaire de Nanoscience de Marseille (FR)
Ministère de l'Enseignement Supérieur et de la Recherche, Centre National de la Recherche Scientifique
Openalex Percentile: Top 39%
Organic Electronics and Photovoltaics
0.42
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Tuning the Electronic Properties of Bridged Dithienyl‐, Difuryl‐, Dipyrrolyl‐Vinylene as Precursors of Small‐Bandgap Conjugated Polymer. — Tommaso Nicolini, Jean‐Marc Sotiropoulos, et al. · Chemistry - A European Journal (2024) | TGRS Research Map | TGRS