Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 Main types of initiation reaction  





2 Safety  





3 References  














Radical initiator






العربية
Azərbaycanca
Bosanski
Čeština
Deutsch
Eesti
Ελληνικά
Euskara
فارسی
Français

Português
Suomi

 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 




In other projects  



Wikimedia Commons
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


Inchemistry, radical initiators are substances that can produce radical species under mild conditions and promote radical reactions.[1] These substances generally possess weak bonds—bonds that have small bond dissociation energies. Radical initiators are utilized in industrial processes such as polymer synthesis. Typical examples are molecules with a nitrogen-halogen bond, azo compounds, and organic and inorganic peroxides.[2]

Main types of initiation reaction

[edit]
AIBN initiator
[O3SO-OSO3]2− ⇌ 2 [SO4]

The sulfate radical adds to an alkene forming radical sulfate esters, e.g. .CHPhCH2OSO3, that add further alkenes via formation of C-C bonds. Many styrene and fluoroalkene polymers are produced in this way.

General ATRP Reaction. A. Initiation. B. Equilibrium with dormant species. C.Propagation

Safety

[edit]

Some radical initiators such as azo compounds and peroxides can detonate at elevated temperatures so they must be stored cold.

References

[edit]
  1. ^ March, Jerry (1985), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure, 3rd edition, New York: Wiley, ISBN 9780471854722, OCLC 642506595
  • ^ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, ISBN 978-0-471-72091-1
  • ^ Harald Jakob, Stefan Leininger, Thomas Lehmann, Sylvia Jacobi, Sven Gutewort. "Peroxo Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_177.pub2. ISBN 978-3527306732.{{cite encyclopedia}}: CS1 maint: multiple names: authors list (link)

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Radical_initiator&oldid=1113729180"

    Category: 
    Radical initiators
    Hidden categories: 
    CS1 maint: multiple names: authors list
    Articles with short description
    Short description is different from Wikidata
     



    This page was last edited on 3 October 2022, at 00:25 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki