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On the Study of Catalytic Cross-Coupling Reactions by Amine or Phosphine Ligated Nickel and Palladium Complexes

We successfully synthesize three different tertiary amine phosphinoamine ligands, which are 1-(2-(dicyclohexylphosphino)phenyl)pyrrole (L2), N-(2-(dicyclohexylphosphino)phenyl) morpholine (L3), and N-(2-(diisopropylphosphino)phenyl)morpholine (L4) separately. With another referenced ligand o-(dicyclohexylphosphino)biphenyl (L1) as comparison and test the reactivities toward palladium and nickel by in situ method with the four different ligands.
We test Kumada-Corriu coupling reactivity of different nickel precursors to L1, L2 and L3, surprisingly, we find that under room temperature, reaction of NiCl2(DME) as precursor and TMEDA (1.1 equiv.) as ligand to replace phosphinoamine ligands (L1¡BL2¡BL3) can effectively couple iododecane with hexyllmagnesium bromide, and the catalytic condition possesses quite high selectivity. This new Ni-catalyzed cross-coupling reactions employing secondary isopropylmagnesium chloride have led to the exclusive formation of linear isomerized cross-coupling products due to reinsertion after rapid £]-H elimination.

Identiferoai:union.ndltd.org:NSYSU/oai:NSYSU:etd-0724112-112013
Date24 July 2012
CreatorsKao, Ting-Yin
ContributorsDong, T.-Y., Liang, L.-C., Wu, M.-J., Lee, T.-Y.
PublisherNSYSU
Source SetsNSYSU Electronic Thesis and Dissertation Archive
LanguageCholon
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0724112-112013
Rightsuser_define, Copyright information available at source archive

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