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Subtle structural changes in octupolar merocyanine dyes influence the photosensitized production of singlet oxygen

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Abstract

The photophysical properties of two indoline-based octupolar merocyanine dyes and of the corresponding quinoline-based dyes were examined. This seemingly subtle structural change in the chromophore of these molecules has an appreciable effect on the yields with which these respective compounds sensitize the production of singlet molecular oxygen, O2(a1?g). The indoline-based dyes are reasonably efficient O2(a1?g) sensitizers (?? ~ 0.35), whereas the quinoline-based dyes are poor O2(a1?g) sensitizers (?? ~ 0.005). A series of experiments, including Laser-Induced Optoacoustic Calorimetric (LIOAC) measurements, reveal that this difference principally reflects the fact that the excited singlet state of the quinoline-based dyes rapidly and efficiently decays via nonradiative channels to regenerate the ground state molecule. It is likely that a charge-transfer state mediates this efficient coupling between the excited and ground states. Such subtle, structure-dependent effects are important in elucidating and ultimately understanding phenomena that influence the efficiency of photosensitized O2(a1?g) production. In turn, the knowledge gained facilitates the rational design and preparation of O2(a1?g) sensitizers with explicitly controlled properties.

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References

  1. H. K. Ledford and K. K. Niyogi, Singlet oxygen and photo-oxidative stress management in plants and algae, Plant, Cell Environ., 2005, 28, 1037–1045.

    Article  CAS  Google Scholar 

  2. A. Krieger-Liszkay, Singlet oxygen production in photosynthesis, J. Expt. Bot., 2004, 56, 337–346.

    Article  Google Scholar 

  3. R. Bonnett, Chemical Aspects of Photodynamic Therapy, Gordon and Breach Science Publishers, Amsterdam, 2000.

    Book  Google Scholar 

  4. C. Schweitzer and R. Schmidt, Physical Mechanisms of Generation and Deactivation of Singlet Oxygen, Chem. Rev., 2003, 103, 1685–1757.

    Article  CAS  Google Scholar 

  5. M. Westberg, L. Holmegaard, F. M. Pimenta, M. Etzerodt and P. R. Ogilby, Rational Design of an Efficient, Genetically Encodable, Protein-Encased Singlet Oxygen Photosensitizer, J. Am. Chem. Soc., 2015, 137, 1632–1642.

    Article  CAS  Google Scholar 

  6. F. Wilkinson, W. P. Helman and A. B. Ross, Quantum Yields for the Photosensitized Formation of the Lowest Electronically Excited Singlet State of Molecular Oxygen in Solution, J. Phys. Chem. Ref. Data, 1993, 22, 113–262.

    Article  CAS  Google Scholar 

  7. R. W. Redmond and J. N. Gamlin, A compilation of singlet oxygen yields from biologically relevant molecules, Photochem. Photobiol., 1999, 70, 391–475.

    Article  CAS  Google Scholar 

  8. Y. M. Poronik, V. Hugues, M. Blanchard-Desce and D. T. Gryko, Octupolar Merocyanine Dyes: A New Class of Nonlinear Optical Chromophores, Chem.–Eur. J., 2012, 18, 9258–9266.

    Article  CAS  Google Scholar 

  9. E. Pottier, M. Sergent, R. P. T. Luu and R. Guglielmetti, Synthese De Quelques Spiro[Indoline-Naphtoxazines] Et Spiro [Indoline-Pyridobenzoxazines] Photochromiques, Bull. Soc. Chim. Belg., 1992, 101, 719–739.

    Article  CAS  Google Scholar 

  10. J. H. Chong, M. Sauer, B. O. Patrick and M. J. MacLachlan, Highly Stable Keto-Enamine Salicylideneanilines, Org. Lett., 2003, 5, 3823–3826.

    Article  Google Scholar 

  11. M. Wang, M. Gao, K. D. Miller, G. W. Sledge, G. D. Hutchins, Q.-H. Zheng, Simple synthesis of carbon-11 labeled styryl dyes as new potential PET RNA-specific living cell imaging probes, Eur. J. Medchem., 2009, 44, 2300–2306.

    Article  CAS  Google Scholar 

  12. J. Arnbjerg, M. Johnsen, P. K. Frederiksen, S. E. Braslavsky and P. R. Ogilby, Two-Photon Photosensitized Production of Singlet Oxygen: Optical and Optoacoustic Characterization of Absolute Two-Photon Absorption Cross Sections for Standard Sensitizers in Different Solvents, J. Phys. Chem. A, 2006, 110, 7375–7385.

    Article  CAS  Google Scholar 

  13. P. Salice, J. Arnbjerg, B. W. Pedersen, R. Toftegaard, L. Beverina, G. A. Pagani and P. R. Ogilby, Photophysics of Squaraine Dyes: Role of Charge-Transfer in Singlet Oxygen Production and Removal, J. Phys. Chem. A, 2010, 114, 2518–2525.

    Article  CAS  Google Scholar 

  14. T. Keszthelyi, D. Weldon, T. N. Andersen, T. D. Poulsen, K. V. Mikkelsen and P. R. Ogilby, Radiative Transitions of Singlet Oxygen: New Tools, New Techniques, and New Interpretations, Photochem. Photobiol., 1999, 70, 531–539.

    Article  CAS  Google Scholar 

  15. J. Arnbjerg, M. J. Paterson, C. B. Nielsen, M. Jørgensen, O. Christiansen and P. R. Ogilby, One- and Two-Photon Photosensitized Singlet Oxygen Production: Characterization of Aromatic Ketones as Sensitizer Standards, J. Phys. Chem. A, 2007, 111, 5756–5767.

    Article  CAS  Google Scholar 

  16. P. Seybold and M. Gouterman, Porphyrins XIII: Fluorescence Spectra and Quantum Yields, J. Mol. Spectrosc., 1969, 31, 1–13.

    Article  CAS  Google Scholar 

  17. R. D. Scurlock, S. Nonell, S. E. Braslavsky and P. R. Ogilby, Effect of Solvent on the Radiative Decay of Singlet Molecular Oxygen (a1?g), J. Phys. Chem., 1995, 99, 3521–3526.

    Article  CAS  Google Scholar 

  18. R. D. Scurlock, D. O. Mártire, P. R. Ogilby, V. L. Taylor and R. L. Clough, Quantum Yield of Photosensitized Singlet Oxygen (a1?g) Production in Solid Polystyrene, Macromolecules, 1994, 27, 4787–4794.

    Article  CAS  Google Scholar 

  19. R. Schmidt, C. Tanielian, R. Dunsbach and C. Wolff, Phenalenone, a Universal Reference Compound for the Determination of Quantum Yields of Singlet Oxygen Sensitization, J. Photochem. Photobiol., A, 1994, 79, 11–17.

    Article  CAS  Google Scholar 

  20. N. J. Turro, V. Ramamurthy and J. C. Scaiano, Principles of Molecular Photochemistry, University Science Books, Sausalito, 2009.

    Google Scholar 

  21. S. E. Braslavsky and G. E. Heibel, Time-Resolved Photothermal and Photoacoustic Methods Applied to Photoinduced Processes in Solution, Chem. Rev., 1992, 92, 1381–1410.

    Article  CAS  Google Scholar 

  22. T. Suzuki, Y. Kajii, K. Shibuya and K. Obi, Calorimetric standards for photothermal methods in ultraviolet and visible spectral regions, Res. Chem. Intermed., 1991, 15, 261–270.

    Article  CAS  Google Scholar 

  23. N. P. Ernsting, Transient Optical Absorption Spectroscopy of the Photochemical Spiropyran-Merocyanine Conversion, Chem. Phys. Lett., 1989, 159, 526–531.

    Article  CAS  Google Scholar 

  24. A. K. Chibisov, H. Görner, Photoprocesses in Spiropyran-Derived Merocyanines, J. Phys. Chem. A, 1997, 101, 4305–4312.

    Article  CAS  Google Scholar 

  25. J. Buback, M. Kullmann, F. Langhojer, P. Nuernberger, R. Schmidt, F. Würthner and T. Brixner, Ultrafast Bidirectional Photoswitching of a Spiropyran, J. Am. Chem. Soc., 2010, 132, 16510–16519.

    Article  CAS  Google Scholar 

  26. S. P. McGlynn, T. Azumi and M. Kinoshita, Molecular Spectroscopy of the Triplet State, Prentice-Hall, Englewood Cliffs, 1969.

    Google Scholar 

  27. P.-G. Jensen, J. Arnbjerg, L. P. Tolbod, R. Toftegaard and P. R. Ogilby, Influence of an Intermolecular Charge-Transfer State on Excited-State Relaxation Dynamics: Solvent Effect on the Methylnaphthalene-Oxygen System and its Significance for Singlet Oxygen Production, J. Phys. Chem. A, 2009, 113, 9965–9973.

    Article  CAS  Google Scholar 

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Correspondence to Daniel T. Gryko.

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Electronic supplementary information (ESI) available: NMR spectra and X-Ray crystallographic data of compounds synthesized. CCDC 1057779. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5pp00080g

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Bregnhøj, M., Pimenta, F.M., Poronik, Y.M. et al. Subtle structural changes in octupolar merocyanine dyes influence the photosensitized production of singlet oxygen. Photochem Photobiol Sci 14, 1138–1146 (2015). https://doi.org/10.1039/c5pp00080g

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  • DOI: https://doi.org/10.1039/c5pp00080g

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