AI Article Synopsis

  • Two dyads were created using tetraarylpyrrolo[3,2-b]pyrrole (TAPP) as a blue energy donor and BODIPY, with different connection methods: direct in dyad 1 and through phenylethynyl linkers in dyad 2.
  • This is the first time TAPP has been reported as an energy donor in combination with BODIPY, showing over 99.9% quenching of TAPP fluorescence, indicating efficient energy transfer.
  • Energy transfer rates were measured at 125 femtoseconds for dyad 1 and 480 femtoseconds for dyad 2, with theoretical models helping to explain the differences in their performance, suggesting potential for

Article Abstract

We have synthesized two dyads (dyad 1 and 2) comprising of tetraarylpyrrolo[3,2-b]pyrrole (TAPP) and BODIPY. In dyad 1, two BODIPYs are directly connected with TAPP moiety whereas in dyad 2, BODIPYs are connected through phenylethynyl linkers. TAPP is a blue energy donor which is easy to synthesize and functionalize as compared to other well-known blue energy donors like pyrene, perylene etc. This is the first report of using TAPP as an energy donor in BODIPY based dyad molecules. Complete quenching of TAPP fluorescence in the dyads suggests fast energy transfer from TAPP to BODIPY unit (ETE~99.9 %). Ultrafast fluorescence and transient absorption spectroscopic studies of dyad 1 showed TAPP to BODIPY energy transfer in 125 fs (k=8.0×10 s) which is one of the fastest energy transfer events in BODIPY based dyad reported so far. Whereas, in dyad 2, energy transfer is almost four times slower (480 fs, k=2.1×10 s). These results were rationalized by theoretical Förster formulations. This study shows that suitably matched optical properties of TAPP and BODIPY dyes along with their easy syntheses will be the key to develop highly efficient energy transfer systems in future for multiple applications.

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Source
http://dx.doi.org/10.1002/chem.202402669DOI Listing

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