Document Type

Article

Disciplines

Optics, 1.4 CHEMICAL SCIENCES

Publication Details

From Journal of Materials Chemistry C:

https://doi.org/10.1039/d3tc02640j

Abstract

A series of new heavy-atom-free photosensitizers based on 2,6-diethoxycarbonyl-BODIPY scaffold was designed and applied for holographic recording in a photopolymerizable material. Photoinduced electron transfer between the BODIPY and meso-aryl subunits, followed by the formation of BODIPY triplet excited states via spin-orbit charge transfer intersystem crossing (SOCT-ISC) was studied by steady-state and ultrafast pump-probe transient optical spectroscopy. Highly efficient photosensitization was observed for dyads bearing pyrene and anthracene substituents, which exhibited singlet oxygen generation quantum yields () of up to 94%. Charge transfer and SOCT-ISC were observed in non-polar solvent (toluene) due to the increased electron accepting ability of the diethoxycarbonyl-BODIPY. In combination with N-phenylglycin (NPG) as a co-initiator, new BODIPYs initiate a free-radical polymerization of acrylamide monomers under 532 nm irradiation that was used for creation of volume phase transmission gratings in a photopolymerizable material based on cellulose acetate and polyethylene glycol (CA-PEG). As a result of holographic recording, diffractive structures with diffraction efficiency of up to 56% were obtained for CA-PEG layers sensitized with BODIPY-pyrene dyad as compared to a reference heavy-atom-containing diiodo-BODIPY dye (27%). The developed materials showed refractive index modulation of up to 2.3 × 10-3, which demonstrate the potential of diethoxycarbonyl-BODIPYs photosensitizers for holographic recording applications.

DOI

https://doi.org/10.1039/d3tc02640j

Funder

Science Foundation Ireland

Creative Commons License

Creative Commons Attribution-NonCommercial 4.0 International License
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License

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