| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1323044 | Journal of Organometallic Chemistry | 2012 | 7 Pages |
New imino-imidazole ligands bearing a pendant donor function L were synthesized in excellent yields. The corresponding nickel(II) complexes [NiCl2(imino-imidazole-L)]n (L = (CH2)2SMe (2a), (CH2)2OMe (2b), (CH2)2NEt2 (2c), (CH2)2PPh2 (2d), (C6H4)-p-OMe (2e), (CH2)3OMe (2f), (CH2)3CH3 (2g); n = 1, 2) were prepared and characterized by FT-IR spectroscopy and elemental analysis. Furthermore, the coordination geometry around the metal center in the dinuclear complex 2a and the mononuclear complexes 2c and 2e was unambiguously established by single crystal X-ray diffraction. All complexes have been evaluated for the oligomerization of ethylene in the presence of EtAlCl2 or MAO (methylaluminoxane) as cocatalyst, and mostly dimers and trimers were produced. Better activities were observed with EtAlCl2 as cocatalyst than with MAO.
Graphical abstractA series of imino-imidazole ligands bearing a pendant donor function L were synthesized. The corresponding nickel complexes were characterized and led to active catalysts in the oligomerization of ethylene upon activation with EtAlCl2 or MAO.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► New imino-imidazole ligands bearing a pendant donor function L were synthesized. ► The tridentate coordination fashion of the ligands on nickel center is established by X-ray diffraction. ► Better activities are obtained with precatalysts activated with EtAlCl2 than with MAO.
