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Ligand and Gold(I) Fluorescein–AIEgens as Photosensitizers in Solution and Doped Polymers

[Image: see text] The synthesis of fluorescein propargyl diether (L) and two different dinuclear gold(I) derivatives containing a water-soluble phosphane [1,3,5-triaza-7-phosphatricyclo[3.3.1.13.7]decane (PTA) for complex 1 and 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane (DAPTA) for comp...

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Autores principales: Pinto, Andrea, Llanos, Alejandro, Gomila, Rosa M., Frontera, Antonio, Rodríguez, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189736/
https://www.ncbi.nlm.nih.gov/pubmed/37139684
http://dx.doi.org/10.1021/acs.inorgchem.3c00197
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author Pinto, Andrea
Llanos, Alejandro
Gomila, Rosa M.
Frontera, Antonio
Rodríguez, Laura
author_facet Pinto, Andrea
Llanos, Alejandro
Gomila, Rosa M.
Frontera, Antonio
Rodríguez, Laura
author_sort Pinto, Andrea
collection PubMed
description [Image: see text] The synthesis of fluorescein propargyl diether (L) and two different dinuclear gold(I) derivatives containing a water-soluble phosphane [1,3,5-triaza-7-phosphatricyclo[3.3.1.13.7]decane (PTA) for complex 1 and 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane (DAPTA) for complex 2] has been successfully performed. All compounds display intrinsic emission from fluorescein, being less intense for gold(I) complexes due to the heavy-atom effect. All compounds aggregate in acetonitrile/water mixtures with the formation of larger aggregates for those samples containing more water content, as evidenced by dynamic light scattering and small-angle X-ray scattering experiments, in agreement with the absorption and emission data. The emission of the samples increases when they are used to obtain luminescent materials with four different organic matrices [poly(methyl methacrylate, polystyrene (PS), cellulose, and Zeonex]. The compounds display very high values of singlet oxygen ((1)O(2)) production in dichloromethane. Singlet oxygen production was also evaluated in the doped matrices, being the highest in PS and with an exciting increase on PS microspheres. Density functional theory (BP86-D3) and GFN2-xTB calculations were used to model the assembly of L and complexes 1 and 2 with the different organic matrices and rationalize the experimental findings based on the geometries, molecular electrostatic potential surfaces, and complementarity and HOMO–LUMO gaps.
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spelling pubmed-101897362023-05-18 Ligand and Gold(I) Fluorescein–AIEgens as Photosensitizers in Solution and Doped Polymers Pinto, Andrea Llanos, Alejandro Gomila, Rosa M. Frontera, Antonio Rodríguez, Laura Inorg Chem [Image: see text] The synthesis of fluorescein propargyl diether (L) and two different dinuclear gold(I) derivatives containing a water-soluble phosphane [1,3,5-triaza-7-phosphatricyclo[3.3.1.13.7]decane (PTA) for complex 1 and 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane (DAPTA) for complex 2] has been successfully performed. All compounds display intrinsic emission from fluorescein, being less intense for gold(I) complexes due to the heavy-atom effect. All compounds aggregate in acetonitrile/water mixtures with the formation of larger aggregates for those samples containing more water content, as evidenced by dynamic light scattering and small-angle X-ray scattering experiments, in agreement with the absorption and emission data. The emission of the samples increases when they are used to obtain luminescent materials with four different organic matrices [poly(methyl methacrylate, polystyrene (PS), cellulose, and Zeonex]. The compounds display very high values of singlet oxygen ((1)O(2)) production in dichloromethane. Singlet oxygen production was also evaluated in the doped matrices, being the highest in PS and with an exciting increase on PS microspheres. Density functional theory (BP86-D3) and GFN2-xTB calculations were used to model the assembly of L and complexes 1 and 2 with the different organic matrices and rationalize the experimental findings based on the geometries, molecular electrostatic potential surfaces, and complementarity and HOMO–LUMO gaps. American Chemical Society 2023-05-04 /pmc/articles/PMC10189736/ /pubmed/37139684 http://dx.doi.org/10.1021/acs.inorgchem.3c00197 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Pinto, Andrea
Llanos, Alejandro
Gomila, Rosa M.
Frontera, Antonio
Rodríguez, Laura
Ligand and Gold(I) Fluorescein–AIEgens as Photosensitizers in Solution and Doped Polymers
title Ligand and Gold(I) Fluorescein–AIEgens as Photosensitizers in Solution and Doped Polymers
title_full Ligand and Gold(I) Fluorescein–AIEgens as Photosensitizers in Solution and Doped Polymers
title_fullStr Ligand and Gold(I) Fluorescein–AIEgens as Photosensitizers in Solution and Doped Polymers
title_full_unstemmed Ligand and Gold(I) Fluorescein–AIEgens as Photosensitizers in Solution and Doped Polymers
title_short Ligand and Gold(I) Fluorescein–AIEgens as Photosensitizers in Solution and Doped Polymers
title_sort ligand and gold(i) fluorescein–aiegens as photosensitizers in solution and doped polymers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10189736/
https://www.ncbi.nlm.nih.gov/pubmed/37139684
http://dx.doi.org/10.1021/acs.inorgchem.3c00197
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