Cookies Policy

This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies.

I accept this policy

Find out more here

Intramolecular Charge Delocalization in the Singlet Excited State of Blocked Pyrylium Ions

No metrics data to plot.
The attempt to load metrics for this article has failed.
The attempt to plot a graph for these metrics has failed.
The full text of this article is not currently available.

Brill’s MyBook program is exclusively available on BrillOnline Books and Journals. Students and scholars affiliated with an institution that has purchased a Brill E-Book on the BrillOnline platform automatically have access to the MyBook option for the title(s) acquired by the Library. Brill MyBook is a print-on-demand paperback copy which is sold at a favorably uniform low price.

Access this article

+ Tax (if applicable)
Add to Favorites
You must be logged in to use this functionality

image of Research on Chemical Intermediates

The dual fluorescence emission of the pyrylium ion 3 and of the partly blocked 4 has been studied extensively under various conditions. The short-wavelength emitting species N* of 3 is short-lived ( 200 ps at room temperature) while the long-wavelength emitting species A* is long-lived (> 3 ns, except in acetic acid). This long-wavelength fluorescence undergoes an important solvatochromic shift and the difference ΔŪ , between the absorption and fluorescence maxima versus Lippert's solvent polarity function Δf is linear. Increasing the viscosity of the medium, or decreasing the temperature, decreases the long-wavelength emission quantum yield while that of the short-wavelength fluorescence and its lifetime (from < 100 ps to > 4 ns) both increase, indicating that A* is formed from N*. Introducing an ortho methyl group on the paraanisyl substituent (compound 4) blocks its rotation and reduces the fluorescence IA. / IN. ratio, but it does not suppress completely the long-wavelength emission. This favors a ground state configuration where the phenyl substituent would be orthogonal to the xanthylium moiety. A strong interaction of 3 and 4 with aliphatic nitriles is characterized from the quenching of the fluorescence emission (with rate constants of ca. 2 x 108 M-1 s-1). A static quenching process also occurs indicating a ground state interaction with the solvent. In pure aliphatic nitriles, this interaction is the main deactivation pathway of the singlet excited state, and practically no fluorescence nor triplet formation can be observed. An important effect of the position where the methoxy group is bound to the molecule is pointed out.

Affiliations: 1: Laboratoire des Matériaux Moléculaires, U.P.R. 241 du C.N.R.S., 2-8 rue H. Dunant, 94320 - Thiais, France


Full text loading...


Data & Media loading...

Article metrics loading...



Can't access your account?
  • Tools

  • Add to Favorites
  • Printable version
  • Email this page
  • Subscribe to ToC alert
  • Get permissions
  • Recommend to your library

    You must fill out fields marked with: *

    Librarian details
    Your details
    Why are you recommending this title?
    Select reason:
    Research on Chemical Intermediates — Recommend this title to your library
  • Export citations
  • Key

  • Full access
  • Open Access
  • Partial/No accessInformation