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Spectral and luminescent properties of triareno-substituted tetraazachlorins

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Journal of Applied Spectroscopy Aims and scope

Spectral and luminescent properties of recently synthesized compounds of a class of hydroporphyrazines, triarenotetraazachlorins, in polyvinylbutyral films have been studied. Fluorescence lifetimes have been measured in film and in solution. Fluorescence quantum yields have been estimated. It is found that annelation of aromatic rings to the pyrrole rings of the tetraazachlorin macrocycle enhances fluorescence. Quantum-chemical optimization of the geometrical structures of the free-base 1,2-trinaphthotetraazachlorins has been carried out using the AM1 method. The two isomers were shown to be highly non-planar. Spectral hole burning in absorption bands of both this compound and free-base 2,3-trinaphthotetraazachlorin in polyvinylbutyral films at 5 K in the wavelength region of titanium-sapphire laser radiation is possible and is ascribed to NH-photoisomerization.

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Authors and Affiliations

  1. Belarusian State Agrarian Technical University, 99 Nezavisimosti Ave., 220023, Minsk, Belarus

    S. M. Arabei

  2. Laboratoire Aime′ Cotton, Centre Universitaire d’Orsay, Orsay, France

    J.-P. Galaup

  3. B. I. Stepanov Institute of Physics, National Academy of Sciences of Belarus, Minsk, Belarus

    A. P. Stupak, T. A. Pavich & K. N. Solovyov

  4. Organic Intermediates and Dyes Institute (NIOPIK), Moscow, Russia

    E. A. Makarova

Authors
  1. S. M. Arabei
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  2. J.-P. Galaup
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  3. A. P. Stupak
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  4. T. A. Pavich
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  5. E. A. Makarova
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  6. K. N. Solovyov
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Correspondence to S. M. Arabei.

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Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 76, No. 3, pp. 376–386, May–June, 2009.

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Arabei, S.M., Galaup, JP., Stupak, A.P. et al. Spectral and luminescent properties of triareno-substituted tetraazachlorins. J Appl Spectrosc 76, 352–361 (2009). https://doi.org/10.1007/s10812-009-9187-x

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  • DOI: https://doi.org/10.1007/s10812-009-9187-x

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