Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1315726 | Journal of Fluorine Chemistry | 2006 | 4 Pages |
Abstract
A series of nickel-salicylideneimines complexes were prepared in wild way and these complexes were stable to air and moisture. The nickel-salicylideneimines complexes exhibited good activity in catalyzing Grignard reagents with aryl halids to biphenyl derivatives and the more fluorine atoms contained by N-substituted benzene moiety could function the better activity.
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Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Jing-Wei Zhao, Li-Ping Song, Yong-Kang Wang, Shi-Zheng Zhu,