EventsThe 26th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session S1. General Organic Synthesis of the event The 26th International Electronic Conference on Synthetic Organic Chemistry
Published date
17 Nov, 2022
Academic Editor
author-avatarJulio A. Seijas
Citation
Beatriz L. Maroto, Sergio Serrano, Josué Jiménez, Ruth Prieto-Montero, Florencio Moreno, Virginia Martínez-Martínez, Santiago de la Moya, Exploring BINOL-O-BODIPY-based dimers as advanced chromophoric platforms enabling triplet state population, in Proceedings of The 26th International Electronic Conference on Synthetic Organic Chemistry, 15 November–30 November 2022, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-26-13671
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Exploring BINOL-O-BODIPY-based dimers as advanced chromophoric platforms enabling triplet state population

Sergio Serrano 1
Josué Jiménez 1
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1. Dpto. Química Orgánica I. Facultad de Ciencias Químicas. Universidad Complutense de Madrid. Ciudad Universitaria s/n, 28040 Madrid, Spain
2. Departamento de Química Física, Facultad de Ciencia y Tecnología. Universidad del País Vasco, 48080 Bilbao, Spain
3. Departamento de Química Física, Facultad de Ciencia y Tecnología Universidad del País Vasco, 48080 Bilbao, Spain
Abstract

The development of chromophoric systems that populate triplet states upon light absorption, i.e. triplet state photosensitizers (TS-PSs), has great interest for many applications in diverse fields beyond Organic Photochemistry, such as Biomedicine (e.g., in singlet-oxygen-based photodynamic therapy, PDT, and phototheranosis) or Sustainable Energy (e.g., in photocatalytic water splitting). Despite the high fluorescence of the BODIPY (boron dipyrromethene) dyes, they can be suitable and valuable candidates as advanced TS-PS scaffolds, owing to their outstanding light-absorption capability and their tuneability by workable organic chemistry, as well as to the existence of well-known designing strategies to promote the required intersystem crossing (ISC) towards the TS. Among these strategies, the use of heavy atoms, such as iodine or heavy metals is one of the most used. However, these dyes usually suffer from the potential toxicity of said heavy atoms, limiting their application in Biomedicine. Another approach is based on the construction of orthogonal (directly-linked) BODIPY dimers, although this strategy is not general and usually requires complex syntheses. Additionally, modulating the population of intramolecular charge transfer (ICT) states in BODIPYs has emerged as a potential tool for designing TS-PSs, since ICT states can serve as runways promoting the ISC. Among these ICT-modulable-BODIPYs, two easily-accessible designs have been studied: meso-meso p-phenylene-bridged BODIPY-BODIPY dimers and BINOL-O-BODIPYs. In this context, we hypothesized that putting both designs together within the same molecule could be a potential strategy to boost triplet population in heavy-atom-free BODIPYs. This communication shows preliminary results related to this investigation, concerning the design, synthesis and photophysical characterization, including fluorescence and singlet oxygen generation, of the new dyes combining both features.

Keywords
Keywords: BODIPY
Triplet state
Photosensitizer
Fluorescence
Singlet Oxygen
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