Research on Chemical Intermediates

, 35:939

UV absorption and fluorescence properties of fused aromatic hydrocarbons having trimethylsilyl, trimethylgermyl, and trimethylstannyl groups

  • Hajime Maeda
  • Hideki Ishida
  • Yohtaro Inoue
  • Abdurisit Merpuge
  • Tomohiro Maeda
  • Kazuhiko Mizuno
Article

DOI: 10.1007/s11164-009-0076-y

Cite this article as:
Maeda, H., Ishida, H., Inoue, Y. et al. Res Chem Intermed (2009) 35: 939. doi:10.1007/s11164-009-0076-y

Abstract

Effects of trimethylsilyl, trimethylgermyl, and trimethylstannyl substituents attached to fused aromatic hydrocarbons such as pyrene, anthracene, phenanthrene, and naphthalene were studied in terms of UV absorption and fluorescence properties in aerated cyclohexane solutions. Absorption maxima of trimethylsilyl-, trimethylgermyl-, and trimethylstannyl-substituted aromatic hydrocarbons shifted to longer wavelengths than those of unsubstituted ones. Absorption maxima of mono-, bis-, tris-, and tetrakis(trimethylsilyl)pyrenes shifted to longer wavelength consecutively at intervals of 10 nm. Fluorescence intensities and fluorescence lifetimes of trimethylsilyl-substituted aromatic hydrocarbons were larger and longer than those of unsubstituted ones, and they decreased in the order of Me3SiAr > Me3GeAr > Me3SnAr. Fluorescence intensity of 1,3,6,8-tetrakis(trimethylsilyl)pyrene was largest among those of a series of mono-, bis-, tris-, and tetrakis(trimethylsilyl)pyrenes under aerated conditions.

Keywords

AbsorptionFluorescenceAromatic hydrocarbonsGroup 14 elements

Copyright information

© Springer Science+Business Media BV 2009

Authors and Affiliations

  • Hajime Maeda
    • 1
  • Hideki Ishida
    • 1
  • Yohtaro Inoue
    • 1
  • Abdurisit Merpuge
    • 1
  • Tomohiro Maeda
    • 1
  • Kazuhiko Mizuno
    • 1
  1. 1.Department of Applied Chemistry, Graduate School of EngineeringOsaka Prefecture UniversityOsakaJapan