Study on the intermediate of photooxidative degradation of phenylenevinylene oligomers

Study on the intermediate of photooxidative degradation of phenylenevinylene oligomers The results of the investigation on photooxidative degradation of five phenylenevinylene oligomers are as follows. The sequence of the photodegradation rate in self-sensitized reaction is the same as that in the biacetyl-sensitized reaction and the rate of photooxidative degradation increases upon the incorporation of electron-donating groups and decreases upon the incorporation of electron-accepting groups on the oligomers. The self-sensitized reaction rate of oligomers increases as the solvent changing from benzene to deuterated benzene and decreases with the addition of the singlet oxygen (1O2) scavenger. 1O2 is shown to be the main reactive intermediate in self-sensitized photolysis of phenylenevinylene oligomers, which was directly confirmed by ESR spin trapping experiments. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Study on the intermediate of photooxidative degradation of phenylenevinylene oligomers

Loading next page...
 
/lp/springer_journal/study-on-the-intermediate-of-photooxidative-degradation-of-f8Nn0oOtBP
Publisher
Brill Academic Publishers
Copyright
Copyright © 2001 by VSP 2001
Subject
Chemistry; Inorganic Chemistry; Physical Chemistry
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1163/156856701317051716
Publisher site
See Article on Publisher Site

Abstract

The results of the investigation on photooxidative degradation of five phenylenevinylene oligomers are as follows. The sequence of the photodegradation rate in self-sensitized reaction is the same as that in the biacetyl-sensitized reaction and the rate of photooxidative degradation increases upon the incorporation of electron-donating groups and decreases upon the incorporation of electron-accepting groups on the oligomers. The self-sensitized reaction rate of oligomers increases as the solvent changing from benzene to deuterated benzene and decreases with the addition of the singlet oxygen (1O2) scavenger. 1O2 is shown to be the main reactive intermediate in self-sensitized photolysis of phenylenevinylene oligomers, which was directly confirmed by ESR spin trapping experiments.

Journal

Research on Chemical IntermediatesSpringer Journals

Published: Oct 13, 2004

References

You’re reading a free preview. Subscribe to read the entire article.


DeepDyve is your
personal research library

It’s your single place to instantly
discover and read the research
that matters to you.

Enjoy affordable access to
over 12 million articles from more than
10,000 peer-reviewed journals.

All for just $49/month

Explore the DeepDyve Library

Unlimited reading

Read as many articles as you need. Full articles with original layout, charts and figures. Read online, from anywhere.

Stay up to date

Keep up with your field with Personalized Recommendations and Follow Journals to get automatic updates.

Organize your research

It’s easy to organize your research with our built-in tools.

Your journals are on DeepDyve

Read from thousands of the leading scholarly journals from SpringerNature, Elsevier, Wiley-Blackwell, Oxford University Press and more.

All the latest content is available, no embargo periods.

See the journals in your area

DeepDyve Freelancer

DeepDyve Pro

Price
FREE
$49/month

$360/year
Save searches from
Google Scholar,
PubMed
Create lists to
organize your research
Export lists, citations
Read DeepDyve articles
Abstract access only
Unlimited access to over
18 million full-text articles
Print
20 pages/month
PDF Discount
20% off