Synthesis of new ferrocenyl amine sulfide and selenide complexes of group 10 metals and their catalytic activities toward selective hydrogenation, isomerization, and asymmetric Grignard cross-coupling reactions
| Autor: | Carl H. Brubaker, Ahmad A. Naiini, Chung-Kung Lai, Donald L. Ward |
|---|---|
| Rok vydání: | 1990 |
| Předmět: |
Chemistry
Stereochemistry Organic Chemistry Grignard reaction chemistry.chemical_element Biochemistry Medicinal chemistry Coupling reaction Catalysis Inorganic Chemistry chemistry.chemical_compound Ferrocene Cyclopentadienyl complex Selenide Materials Chemistry Physical and Theoretical Chemistry Metallocene Palladium |
| Zdroj: | Journal of Organometallic Chemistry. 390:73-90 |
| ISSN: | 0022-328X |
| Popis: | Two series of previously unknown ferrocenyl amine sulfide and selenide ligands ( S,R )-[ER]C 5 H 4 FeC 5 H 3 [CHMeNMe 2 ] [ER] and [ER]C 5 H 4 FeC 5 H 3 [CH 2 NMe 2 ]-[ER], where E = S and Se; R = Me, Ph, Bz, 4-tolyl, and 4-ClPh, have been prepared. Lithiation of ( S )-[1-(dimethylamino)ethyl]ferrocene and [(dimethylamino)methyl] ferrocene first in the presence of ether and then TMEDA followed by treatment with different diselenides and disulfides resulted in the synthesis of these new ligands. Palladium and platinum dichloride adducts of these compounds have been prepared from a benzene solution of (PhCN) 2 MCl 2 where M = Pd and Pt. The palladium complexes are active catalysts for selective hydrogenation of dienes to monoenes both under homogeneous and heterogeneous conditions. In the case of hydrogenation of 2,3-dimethyl-1,3-butadiene, isomerization has been observed. Nickel complexes of the new sulfide ligands were prepared in situ and used as catalysts for the asymmetric Grignard cross-coupling reactions. The possible structures of Pd and Pt complexes are discussed. The X-ray crystal structure was determined for [SMe]C 5 H 4 FeC 5 H 3 [CH 2 NMe 2 ][SMe][PdCl 2 ]; it reveals that the Pd atom is coordinated to the S and N atoms of the same cyclopentadienyl ring. |
| Databáze: | OpenAIRE |
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