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Dimethyl group IV metal complexes of the OSO-type ligand bearing AlMe2 moieties.
Autorzy
Rok wydania
2006
Czasopismo
Numer woluminu
25
Strony
6166-6169
DOI
10.1021/om0608051
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
Complexes having two ancillary (tbop)2- ligands where tbopH2 = 2,2‘-thiobis{4-(1,1,3,3-tetramethylbutyl)phenol}, viz., [M(tbop-κ3O,S,O)2] (M = Ti, 1; M = Zr, 2; M = Hf, 3), have been prepared in good yields by amine or HCl elimination from tbopH2. The 1H and 13C NMR studies showed that complexes 1−3 adopt in solution mononuclear structures. Treatment of 1−3 with 2 equiv or an excess of AlMe3 generates heterometallic [M(μ-tbop-κ3O,S,O)2Me2(μ-AlMe2)2] (M = Ti, 4; M = Zr, 5; M = Hf, 6) complexes. The structures of 4−6 were confirmed by NMR spectroscopy; complexes 5 and 6 were further investigated by X-ray crystallography. These studies showed 4−6 to be trimers either in the solid state or in solution. The crystals of 5·CH2Cl2 and 6·CH2Cl2 consist of eight-coordinate dimethyl Zr or Hf centers and two AlMe2 moieties attached to oxygen atoms of the tbop ligands. The saturated coordination sphere of the metal centers in 1−6 makes them inactive in ethene polymerization
Słowa kluczowe
Catalysts, Alkyls, Metals, Ligands, Aluminum
Adres publiczny
https://doi.org/10.1021/om0608051
Strona internetowa wydawcy
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