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 History  





2 Uses  





3 Reactions  





4 References  














4,4'-Bipyridine






العربية
تۆرکجه
Čeština
Deutsch
فارسی
Français

Português
Српски / srpski
Srpskohrvatski / српскохрватски

 

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
 


4,4′-Bipyridine
4,4′-bipyridine
4,4′-Bipyridine molecule
Names
Preferred IUPAC name

4,4′-Bipyridine

Identifiers

CAS Number

3D model (JSmol)

Beilstein Reference

113176
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.008.216 Edit this at Wikidata
EC Number
  • 209-036-3

Gmelin Reference

3759

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C10H8N2/c1-5-11-6-2-9(1)10-3-7-12-8-4-10/h1-8H ☒N

    Key: MWVTWFVJZLCBMC-UHFFFAOYSA-N ☒N

  • c1cnccc1-c2ccncc2

Properties

Chemical formula

C10H8N2
Molar mass 156.188 g·mol−1
Melting point 114 °C (237 °F; 387 K)
Boiling point 305 °C (581 °F; 578 K)
Structure

Dipole moment

D
Related compounds

Related compounds

2,2′-Bipyridine
Pyridine
4-Pyridylnicotinamide
Terpyridine
Biphenyl

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

4,4′-Bipyridine (abbreviated to 4,4′-bipyor4,4′-bpy) is an organic compound with the formula (C5H4N)2. It is one of several isomers of bipyridine. It is a colorless solid that is soluble in organic solvents. is mainly used as a precursor to N,N′-dimethyl-4,4′-bipyridinium [(C5H4NCH3)2]2+, known as paraquat.

History

[edit]

4,4′-Bipyridine was first obtained in 1868 by the Scottish chemist Thomas Anderson via heating pyridine with sodium metal.[1] However, Anderson's empirical formula for 4,4′-bipyridine was incorrect.[2] The correct empirical formula, and the correct molecular structure, for 4,4′-bipyridine was provided in 1882 by the Austrian chemist Hugo Weidel and his student M. Russo.[3]

Uses

[edit]

4,4'-Bipyridine is an intermediate in the production of paraquat, a widely-used herbicide. In this process, pyridine is oxidized to 4,4'-bipyridine in a coupling reaction, followed by dimethylation to form paraquat.[4]

Reactions

[edit]

The reducing agent is N,N'-bis(trimethylsilyl)-4,4'-bipyridinylidene is produced by reduction of 4,4'-bipyridine in the presence of trimethylsilyl chloride (Me = CH3):

NC5H4C5H4N + 2 Li + 2 Me3SiCl → Me3SiNC5H4C5H4NSiMe3 + 2 LiCl

The silylated derivative, which is red, is used in salt-free reductions.[5]

4,4′-bipyridine forms a variety of coordination polymers.[6]

References

[edit]
  1. ^ See:
    • Anderson, Thomas (1868). "On the products of the destructive distillation of animal substances. Part V." Transactions of the Royal Society of Edinburgh. 25: 205–216. doi:10.1017/S0080456800028167. S2CID 251577345. Anderson called 4,4′-bipyridine "Dipyridine".
  • German translation: Anderson, Th. (1870). "Ueber die Producte der trockenen Destillation thierischer Materien. Fünfter Theil" [On the products of the dry distillation of animal materials. Fifth part.]. Annalen der Chemie und Pharmacie (in German). 154: 270–286. doi:10.1002/jlac.18701540303.
  • See also: Fehling, Hermann Christian von, ed. (1890). Neues Handwörterbuch der Chemie [New Concise Dictionary of Chemistry] (in German). Vol. 5. Braunschweig, Germany: Friedrich Vieweg und Sohn. p. 974. See γ-Dipyridyl.
  • ^ Anderson gave the empirical formula for 4,4′-bipyridine as C10H10N2. See:
    • (Anderson, 1868), p. 209.
    • (Fehling, 1890), p. 974 (γ-Dipyridyl).
  • ^ Weidel, H.; Russo, M. (1882). "Studien über das Pyridin" [Studies of pyridine]. Monatshefte für Chemie (in German). 3: 850–885. doi:10.1007/BF01516855. S2CID 97065714. The empirical formula for 4,4′-bipyridine (γ-Dipyridyl) appears on p. 856 ; the molecular structure of 4,4′-bipyridine (γ-Dipyridyl) appears on p. 867.
  • ^ "Paraquat and Diquat". IPCS INCHEM.
  • ^ Tsurugi, Hayato; Mashima, Kazushi (2019). "Salt-Free Reduction of Transition Metal Complexes by Bis(trimethylsilyl)cyclohexadiene, -dihydropyrazine, and -4,4′-bipyridinylidene Derivatives". Accounts of Chemical Research. 52 (3): 769–779. doi:10.1021/acs.accounts.8b00638. PMID 30794373. S2CID 73505603.
  • ^ Biradha, K.; Sarkar, M.; Rajput, L. (2006). "Crystal engineering of coordination polymers using 4,4′-bipyridine as a bond between transition metal atoms". Chemical Communications (40): 4169–79. doi:10.1039/B606184B. PMID 17031423.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=4,4%27-Bipyridine&oldid=1195570373"

    Categories: 
    Bipyridines
    4-Pyridyl compounds
    Substances discovered in the 19th century
    Hidden categories: 
    CS1 German-language sources (de)
    Articles without InChI source
    Articles without KEGG source
    ECHA InfoCard ID from Wikidata
    Articles with changed InChI identifier
    Articles containing unverified chemical infoboxes
    Articles with short description
    Short description matches Wikidata
     



    This page was last edited on 14 January 2024, at 11:20 (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