Repozytorium

Dimethyl group IV metal complexes of the OSO-type ligand bearing AlMe2 moieties.

Autorzy

Dorota Wiśniewska

Zofia Janas

Piotr Sobota

Lucjan B. Jerzykiewicz

Rok wydania

2006

Czasopismo

Organometallics

Numer woluminu

25

Strony

6166-6169

DOI

10.1021/om0608051

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

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 13 adopt in solution mononuclear structures. Treatment of 13 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 46 were confirmed by NMR spectroscopy; complexes 5 and 6 were further investigated by X-ray crystallography. These studies showed 46 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 16 makes them inactive in ethene polymerization

Słowa kluczowe

Catalysts, Alkyls, Metals, Ligands, Aluminum

Adres publiczny

https://doi.org/10.1021/om0608051

Strona internetowa wydawcy

https://www.acs.org/content/acs/en.html

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