4.6 Article

Different Quenching Effect of Intramolecular Rotation on the Singlet and Triplet Excited States of Bodipy

Journal

JOURNAL OF PHYSICAL CHEMISTRY C
Volume 122, Issue 1, Pages 185-193

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.7b10466

Keywords

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Funding

  1. NSFC [21503224, 21673031, 21473020, 21421005]
  2. Fundamental Research Funds for the Central Universities [DUT16TD25, DUT1SZD224, DUT2016TB12]
  3. Guangdong Province Universities and Colleges Young Pearl River Scholar Funded Scheme
  4. Guangzhou Science and Technology Program [201707010243]
  5. Turkish Academy of Sciences (TUBA-GEBIP)
  6. Scientific and Technological Research Council of Turkey (TUBITAK) [114Z790]
  7. Dalian University of Technology

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It is well-known that the fluorescence of a chromophore can be efficiently quenched by the free rotor effect, sometimes called intramolecillar rotation (IMR), i.e. by a large-amplitude torsional motion. Using this effect, aggregation induced enhanced emission (AIE) and fluorescent molecular probes for viscosity measurements have been devised. However, the rotor effect on triplet excited states was rarely studied. Herein, with molecular rotors of Bodipy and diiodoBodipy, and by using steady state and time resolved transient absorption/emission spectroscopies, we confirmed that the triplet excited state-of the Bodipy chromophore is not quenched by IMR. This is in stark contrast to the fluorescence (singlet excited state), which is significantly quenched by IMR. This result is rather interesting since a long-lived excited state (triplet, 276 mu s) is not quenched by the IMR, but the short-lived excited state (singlet, 3.8 ns) is quenched by the same IMR The unquenched triplet excited state of the Bodipy was used for triplet-triplet annihilation upconversion, and the upconversion quantum yield is 6.3%.

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