Synthesis and Properties of Cross‐Shaped Donor–Acceptor Dyes: Tunable Emission From Visible to Near‐Infrared in Solution and Solid‐State

This article reports the synthesis and characterization of cross‐conjugated donor–acceptor dyes based on a N , N , N ’, N ’‐tetraphenyl‐1,4‐phenylenediamine core, substituted at the 2,5‐positions with various electron‐withdrawing groups (carbonyl, imines, nitriles, or electron‐poor heterocycles). Electrochemical studies reveal electronic communication between para ‐substituted donor groups and, in some cases, between acceptor groups. Photophysical studies show tunable absorption and emission properties based on the strength of the electron‐withdrawing groups, a trend that is rationalized through computational analysis. Notably, some compounds exhibit long emission lifetimes in solution, whereas all dyes emit in the solid state, with emission extending into the near‐infrared (up to > 1000 nm).

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2026-06-30
DOI
https://doi.org/10.1002/ejoc.70650
Primary Topic
Luminescence and Fluorescent Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis and Properties of Cross‐Shaped Donor–Acceptor Dyes: Tunable Emission From Visible to Near‐Infrared in Solution and Solid‐State

Olivier Siri, Denis Jacquemin, Benjamin Mourot, Simon Pascal et al.
European Journal of Organic Chemistry
Luminescence and Fluorescent Materials
article

Synthesis and Properties of Cross‐Shaped Donor–Acceptor Dyes: Tunable Emission From Visible to Near‐Infrared in Solution and Solid‐State

Olivier Siri, Denis Jacquemin, Benjamin Mourot, Simon Pascal, Michel Giorgi, Gabriel Canard
article en

Abstract

This article reports the synthesis and characterization of cross‐conjugated donor–acceptor dyes based on a N , N , N ’, N ’‐tetraphenyl‐1,4‐phenylenediamine core, substituted at the 2,5‐positions with various electron‐withdrawing groups (carbonyl, imines, nitriles, or electron‐poor heterocycles). Electrochemical studies reveal electronic communication between para ‐substituted donor groups and, in some cases, between acceptor groups. Photophysical studies show tunable absorption and emission properties based on the strength of the electron‐withdrawing groups, a trend that is rationalized through computational analysis. Notably, some compounds exhibit long emission lifetimes in solution, whereas all dyes emit in the solid state, with emission extending into the near‐infrared (up to > 1000 nm).

European Journal of Organic Chemistry
Centre National de la Recherche Scientifique (FR), Institut Universitaire de France (FR), Chimie et Interdisciplinarité, Synthèse, Analyse, Modélisation (FR), Centrale Méditerranée (FR), Centre Interdisciplinaire de Nanoscience de Marseille (FR), Nantes Université (FR)
Agence Nationale de la Recherche
Openalex Percentile: Top 16%
Luminescence and Fluorescent Materials
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