Journal
DALTON TRANSACTIONS
Volume 43, Issue 5, Pages 2098-2103Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3dt52970c
Keywords
-
Categories
Funding
- 973 Program [2010CB933501, 2011CBA00502]
- Natural Science Foundation of China [21273239]
- Natural Science Foundation of Fujian Province [2011J01064]
- Chinese Academy of Sciences
Ask authors/readers for more resources
The commercially available 2,2'-dipyridylamine was used as a supporting ligand in the palladium-catalyzed Sonogashira cross-coupling reaction. The reactions between aryl iodides and terminal alkynes with different steric hindrance can be efficiently performed in the absence of copper in neat water at room temperature. The superior catalytic performance of the catalytic system was attributed to water solubility of the palladium 2,2'-dipyridylamine complex. Palladium nanoparticles with small size and narrow size distribution were formed after the cross-coupling reaction.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available