Abstract
The reaction of the lithium salt of the aminodiamide ligand Li-2[(SiMe(3))N{CH2CH2N(SiMe(3))}(2)](Li(2)L) (1) with [TiCl4(THF)(2)] (THF = tetrahydrofuran) forms [TiCl2(L)] (2), from which Ti-IV mono and dialkyl complexes are accessible. The treatment of 2 with Me(2)Mg,LiCH2(SiMe(3)) or LiCH(SiMe(3))(2) results in the formation of [TiMe(2)(L)] (3), [Ti{CH2(SiMe(3))}(2)(L)] (4) or [TiCl{CH(SiMe(3))(2)}(L)] (5) respectively, in which only partial coordination of the amino-nitrogen is observed in solution and the solid state. The X-ray crystal structures of 3 and 5, and an improved synthesis of 1, are described.
Original language | English |
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Pages (from-to) | 333-340 |
Number of pages | 8 |
Journal | Journal of organometallic chemistry |
Volume | 501 |
Issue number | 1-2 |
Publication status | Published - 4 Oct 1995 |
Keywords
- TITANIUM
- AMIDE
- ALKYL COMPLEX
- X-RAY STRUCTURE
- NMR SPECTROSCOPY
- MASS SPECTROSCOPY
- M = ZR
- REACTIVITY
- ZIRCONIUM
- HAFNIUM
- HF