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  4. Why are (NN2)Ni pincer complexes active for alkyl-alkyl coupling: ß-H elimination is kinetically accessible but thermodynamically uphill
 
research article

Why are (NN2)Ni pincer complexes active for alkyl-alkyl coupling: ß-H elimination is kinetically accessible but thermodynamically uphill

Breitenfeld, Jan  
•
Vechorkin, Oleg  
•
Corminboeuf, Clémence  
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2010
Organometallics

Isomerization and olefin exchange experiments show that β-H elimination is kinetically viable but thermodynamically unfavorable in [(MeNN2)Ni-alkyl] complexes. The intermediacy of Ni-hydride species was corroborated by a trapping experiment. The alkyl complex [(MeNN2)Ni-propyl] catalyzes olefin isomerization.

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Type
research article
DOI
10.1021/om1007506
Web of Science ID

WOS:000281472500002

Author(s)
Breitenfeld, Jan  
Vechorkin, Oleg  
Corminboeuf, Clémence  
Scopelliti, Rosario  
Hu, Xile  
Date Issued

2010

Publisher

American Chemical Society

Published in
Organometallics
Volume

29

Issue

17

Start page

3686

End page

3689

Subjects

Catalyzed Cross-Couplings

•

Grignard-Reagents

•

Hydride Complexes

•

Nickel-Complexes

•

Halides

•

Bromides

•

Iodides

•

Ligand

•

Ni

•

Hydrosilylation

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCI  
LCMD  
Available on Infoscience
August 12, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/52151
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