2021
DOI: 10.1016/j.dyepig.2021.109382
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Design of flexible dendritic systems bearing donor-acceptor groups (pyrene-porphyrin) for FRET applications

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Cited by 7 publications
(3 citation statements)
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“…Conveniently, the metallation of dendrimer centers of different generations having a molecule suitable (e.g.,porphyrins)forhosting metal ions and pyrene molecules at the periphery has been developed to study their absorption and emission behaviors. The porphyrinicdendrimeric center's complexation of Zn (II) and Mg (II) ions resulted in a red and blue shift of the absorption and emission bands, respectively [166] (Figure 12). Notably, this dendrimers type showed high non-radiative energy-transfer efficiency, reaching values higher than 99%.…”
Section: Dendrimer-based Molecular Systems For Fret Phenomenonmentioning
confidence: 99%
“…Conveniently, the metallation of dendrimer centers of different generations having a molecule suitable (e.g.,porphyrins)forhosting metal ions and pyrene molecules at the periphery has been developed to study their absorption and emission behaviors. The porphyrinicdendrimeric center's complexation of Zn (II) and Mg (II) ions resulted in a red and blue shift of the absorption and emission bands, respectively [166] (Figure 12). Notably, this dendrimers type showed high non-radiative energy-transfer efficiency, reaching values higher than 99%.…”
Section: Dendrimer-based Molecular Systems For Fret Phenomenonmentioning
confidence: 99%
“…Our research group has focused on the study of diverse pyrene systems, such as pyrene-labeled dendronized porphyrins [ 41 ], donor-acceptor molecules with a pyrene-BODIPY architecture [ 42 ], pyrene-porphyrin dyads in flexible dendritic systems, and cyclen-cored star compounds decorated with pyrene and their copper complexes [ 43 ]. Furthermore, we have successfully used FP to prepare fluorescent acrylate polymers containing pyrene and hydrogels containing tetraphenylporphyrin fluorophores [ 44 , 45 , 46 ].…”
Section: Introductionmentioning
confidence: 99%
“…Several lab-made artificial photosynthetic systems comprising naphthyl or pyrenyl moieties covalently tethered to photo- and electro-active entities such as ferrocene, 23–29 porphyrin, 14,30–41 corrole, 16,42–45 perylene, 46–50 borondipyrromethenes (BODIPYs), 51–60 azaBODIPYs, 8,17,61,62 and C 60 63–65 have been synthesized and effectively utilized as light harvesting molecules, 8,14,16,17,34,36,38,47,48,54–56,62,63,66–71 light capturers in dye sensitized solar cells (DSSCs) 30,35,37,40,41,72 and organic solar cells, 46,60,64,65 catalysts in H 2 and O 2 evolution, 44,45 photocatalysts, 32,73 molecular sensors, 23–26,52 sensitizers in photodynamic therapy and singlet oxygen generation, 31,33,59,61 DNA binders, 42 and biological imaging agents, 57 and also for photo-upconversion. 74…”
Section: Introductionmentioning
confidence: 99%