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

Synthesis and photochromism of a novel selenazolyl fulgide

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.

This Article is currently unavailable for purchase.
Add to Favorites
You must be logged in to use this functionality

Cover image Placeholder

Novel fulgides, 5-selenazolyl fulgides, were synthesized and E and Z isomers were directly separated by column chromatography. E↔Z photo-isomerization was only observed during conventional UV light irradiation. Using the pulse laser-photolysis method, photochromic processes were studied. Both the excited singlet state and excited triplet state contribute to photo-cyclization reaction to form the colored form (closed form). The closed form is unstable and quickly goes back to the open form. Solvent has remarkable effect on absorption spectra of the closed form.


Full text loading...


Data & Media loading...

Article metrics loading...



Can't access your account?
  • Key

  • Full access
  • Open Access
  • Partial/No accessInformation