Insights into the Structure–Property Relationship of Difluoro Boron Dipyridomethene Derivatives

To elucidate the molecular structure of the difluoro dipyridomethene system and to establish structure–property relationships, an extensive synthetic work is reported. Four classes of novel fluorescent BF 2 ‐DIPYR complexes are prepared via Suzuki–Miyaura cross‐coupling reaction from the corresponding mono‐ and bis‐brominated dyes in moderate to good yields. The strategy allows the introduction of a large panel of electron‐donating and ‐withdrawing groups on the meso , 3 and/or 7 position of the aromatic BF 2 ‐DIPYR core. The new symmetric and asymmetric mono‐, bis‐, and tris substituted dyes are thoroughly characterized by X‐ray diffraction analysis and spectroscopic measurements. Furthermore, the latter are rationalized by TD‐DFT calculations.

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Publication Details

Journal
ChemPhotoChem
Published
2025-03-17
DOI
https://doi.org/10.1002/cptc.202400395
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.00
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article

Insights into the Structure–Property Relationship of Difluoro Boron Dipyridomethene Derivatives

Camille Chériaux, Gilles Ulrich, Denis Jacquemin, Carlotta Figliola et al.
ChemPhotoChem
Fluorine in Organic Chemistry
article

Insights into the Structure–Property Relationship of Difluoro Boron Dipyridomethene Derivatives

Camille Chériaux, Gilles Ulrich, Denis Jacquemin, Carlotta Figliola, Pascal Retailleau, Thomas V. Papineau
article en

Abstract

To elucidate the molecular structure of the difluoro dipyridomethene system and to establish structure–property relationships, an extensive synthetic work is reported. Four classes of novel fluorescent BF 2 ‐DIPYR complexes are prepared via Suzuki–Miyaura cross‐coupling reaction from the corresponding mono‐ and bis‐brominated dyes in moderate to good yields. The strategy allows the introduction of a large panel of electron‐donating and ‐withdrawing groups on the meso , 3 and/or 7 position of the aromatic BF 2 ‐DIPYR core. The new symmetric and asymmetric mono‐, bis‐, and tris substituted dyes are thoroughly characterized by X‐ray diffraction analysis and spectroscopic measurements. Furthermore, the latter are rationalized by TD‐DFT calculations.

ChemPhotoChemVol. 9(7)
Centre National de la Recherche Scientifique (FR), Institut Universitaire de France (FR), Université Paris-Saclay (FR), Laboratoire de Cristallographie et RMN Biologiques (FR), Institut de Chimie de Strasbourg (FR), Institut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé (FR), Chimie et Interdisciplinarité, Synthèse, Analyse, Modélisation (FR), Université de Strasbourg (FR), Nantes Université (FR)
Openalex Percentile: Top 96%
Fluorine in Organic Chemistry
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Insights into the Structure–Property Relationship of Difluoro Boron Dipyridomethene Derivatives — Camille Chériaux, Gilles Ulrich, et al. · ChemPhotoChem (2025) | TGRS Research Map | TGRS