Tetrathienothiophene Porphyrin as a Metal-Free Sensitizer for Room-Temperature Triplet–Triplet Annihilation Upconversion

Aleksey Vasilev1,2, Anton Kostadinov1, Meglena I. Kandinska2, Katharina Landfester1, Stanislav Baluschev1,3
1Max Planck Institute for Polymer Research, Mainz, Germany
2University of Sofia “Saint Kliment Ohridski”, Faculty of Chemistry and Pharmacy, Sofia, Bulgaria
3University of Sofia “Saint Kliment Ohridski”, Faculty of Physics, Sofia, Bulgaria

Tóm tắt

Optically excited triplet states of organic molecules serve as an energy pool for the subsequent processes, either photon energy downhill, such as room temperature phosphorescence, or photon energy uphill process—the triplet–triplet annihilation upconversion (TTA-UC). Manifestation of a high intersystem crossing coefficient is an unavoidable requirement for triplet state formation, following the absorption of a single photon. This requirement is even more inevitable if the excitation light is non-coherent, with moderate intensity and extremely low spectral power density, when compared with the light parameters of 1 Sun (1.5 AM). Coordination of a heavy atom increases substantially the probability of intersystem crossing. Nevertheless, having in mind the global shortage in precious and rare-earth metals, identification of metal-free organic moieties able to form triplet states becomes a prerequisite for environmental friendly optoelectronic technologies. This motivates us to synthesize a metal-free thienothiophene containing porphyrin, based on a condensation reaction between thienothiophene-2-carbaldehyde and pyrrole in an acidic medium by modified synthetic protocol. The upconversion couple tetrathienothiophene porphyrin/rubrene when excited at λ = 658 nm demonstrates bright, delayed fluorescence with a maximum emission at λ = 555 nm. This verifies our hypothesis that the ISC coefficient in thienothiophene porphyrin is efficient in order to create even at room temperature and low-intensity optical excitation densely populated organic triplet ensemble and is suitable for photon energy uphill processes, which makes this type of metal-free sensitizers even more important for optoelectronic applications.

Từ khóa


Tài liệu tham khảo

Askes, 2018, Solving the Oxygen Sensitivity of Sensitized Photon Upconversion in Life Science Applications, Nat. Rev. Chem., 2, 437, 10.1038/s41570-018-0057-z

Askes, 2017, Water-Dispersible Silica-Coated Upconverting Liposomes: Can a Thin Silica Layer Protect TTA-UC against Oxygen Quenching?, ACS Biomater. Sci. Eng., 3, 322, 10.1021/acsbiomaterials.6b00678

Baluschev, 2016, Annihilation Upconversion in Nanoconfinement: Solving the Oxygen Quenching Problem, Mater. Horiz., 3, 478, 10.1039/c6mh00289g

Baluschev, 2006, Up-Conversion Fluorescence: Noncoherent Excitation by Sunlight, Phys. Rev. Lett., 97, 143903, 10.1103/PhysRevLett.97.143903

Bhyrappa, 2001, Meso-tetrathienylporphyrins: Electrochemical and Axial Ligation Properties, Chem. Phys. Lett., 349, 399, 10.1016/S0009-2614(01)01189-7

Boyle, 2010, Thienyl-Appended Porphyrins: Synthesis, Photophysical and Electrochemical Properties, and Their Applications, Coord. Chem. Rev., 254, 77, 10.1016/j.ccr.2009.09.001

Bugge, 1971, Preparation of Some Methyl- and Formylthieno[2,3-B]thiophenes and Thieno[3,2-B]thiophenes, Acta Chem. Scand., 25, 27, 10.3891/acta.chem.scand.25-0027

Gray, 2018, Towards Efficient Solid-State Triplet-Triplet Annihilation Based Photon Upconversion: Supramolecular, Macromolecular and Self-Assembled Systems, Coord. Chem. Rev., 362, 54, 10.1016/j.ccr.2018.02.011

Guo, 2014, BODIPY Triads Triplet Photosensitizers Enhanced with Intramolecular Resonance Energy Transfer (RET): Broadband Visible Light Absorption and Application in Photooxidation, Chem. Sci., 5, 489, 10.1039/C3SC52323C

Heinrich, 2018, Annihilation Upconversion: Harvesting the Entire Deep-Red Spectral Range of the Sun Irradiation, J. Photonics Energy, 8, 022002, 10.1117/1.JPE.8.022002

Iyisan, 2020, Temperature Sensing in Cells Using Polymeric Upconversion Nanocapsules, Biomacromolecules, 21, 4469, 10.1021/acs.biomac.0c00377

Jin, 2021, Phosphorescence-based Ratiometric Probes: Design, Preparation and Applications in Sensing, Imaging and Biomedicine Therapy, Coord. Chem. Rev., 431, 213694, 10.1016/j.ccr.2020.213694

Koren, 2012, Complexes of IrIII-Octaethylporphyrin with Peptides as Probes for Sensing Cellular O2, ChemBioChem, 13, 1184, 10.1002/cbic.201200083

Kyriakopoulos, 2014, Deposition of Fullerene C60 on the Surface of MCM-41 via the One-step Wet Impregnation Method: Active Catalysts for the Singlet Oxygen Mediated Photooxidation of Alkenes, J. Mol. Catal. A: Chem., 381, 9, 10.1016/j.molcata.2013.09.03610.1016/j.molcata.2013.09.036

Lindsey, 1987, Rothemund and Adler-Longo Reactions Revisited: Synthesis of Tetraphenylporphyrins under Equilibrium Conditions, J. Org. Chem., 52, 827, 10.1021/jo00381a022

Liu, 1977, P-type Delayed Fluorescence from Rubrene, J. Am. Chem. Soc. j, 99, 14, 10.1021/ja00456a011

Mori, 2013, Iridium and Rhodium Complexes within a Macroreticular Acidic Resin: A Heterogeneous Photocatalyst for Visible-Light Driven H2Production without an Electron Mediator, Chem. Asian J., 8, 3207, 10.1002/asia.201301016

Ono, 1998, Synthesis of 3,4-diarylpyrroles and Conversion into Dodecaarylporphyrins; a New Approach to Porphyrins with Altered Redox Potentials, J. Chem. Soc. Perkin Trans. 1, 1, 1595, 10.1039/A801185K

Pristash, 2020, Heavy-Atom-Free Red-To-Yellow Photon Upconversion in a Thiosquaraine Composite, ACS Appl. Energ. Mater., 3, 19, 10.1021/acsaem.9b01808

Shimizu, 2018, Oxidation of Squalene by Singlet Oxygen and Free Radicals Results in Different Compositions of Squalene Monohydroperoxide Isomers, Sci. Rep., 8, 9116, 10.1038/s41598-018-27455-5

Tan, 2021, Phosphorescent Metal Complexes as Theranostic Anticancer Agents: Combining Imaging and Therapy in a Single Molecule, Chem. Sci., 12, 2357, 10.1039/d0sc06885c

Torréns, 1972, Moessbauer Studies on Oxo-Bridged Iron(III) Porphines, J. Am. Chem. Soc., 94, 4160, 10.1021/ja00767a018

Treibs, 1968, Concerning the Synthesis and the Electron Spectrum of Ms-Substituted Porphine, Justus Liebigs Ann. Chem., 718, 183, 10.1002/jlac.19687180118

Yang, 2017, Recent Advances in Organic Thermally Activated Delayed Fluorescence Materials, Chem. Soc. Rev., 46, 915, 10.1039/c6cs00368k

Zhen, 2021, The Development of Phosphorescent Probes for In Vitro and In Vivo Bioimaging, Biomater. Sci., 9, 285, 10.1039/D0BM00819B

Zhou, 2015, Upconversion Luminescent Materials: Advances and Applications, Chem. Rev., 115, 395, 10.1021/cr400478f

Zhou, 2017, Solvent Effects on the Triplet-Triplet Annihilation Upconversion of Diiodo-Bodipy and Peryleneffects on the Triplet–Triplet Annihilation Upconversion of Diiodo-Bodipy and Perylene, Phys. Chem. Chem. Phys., 19, 1516, 10.1039/c6cp06897a

Zhou, 2015, Synthesis and Optical/Electrochemical Properties of Meso-5,10,15,20-Tetrathienyl Substituted Porphyrins and Their Metal Complexes, Asian J. Chem., 27, 616, 10.14233/ajchem.2015.17089