Abstract
Reactions of [(η5-C5Me5)TiCl3] with dialkyl and diarylamido-lithium complexes in 1:1, 1:2 or 1:3 molar ratios afford the mono(pentamethylcyclopentadienyl)titanium(IV) dialkylamido- complexes [(η5-C5Me5)TiCl3-n(NR2)n (n = 1; R = Me or SiMe3) (n = 2, R = Me or Ph) (n = 3, R = Me or Et). Similar reactions of [(η5-C5Me5)TiCl 22(μ-O)] and [(η5-C5Me5)TiCl3(μ-O)3] gave the corresponding complexes [(η5-C5Me5)TiCl2-n(NR2)ni2(μ-O)] (n = 1; R = Me or Ph) (n = 2, R = Me) and [(η5-C5Me5)3Ti3Cl3-n(NMe2)n(μ-O) 3] (n = 1 or 3). The crystal structure of [(η5-C5Me5)Ti(NMe2)3] has been established by X-ray crystallography and is shown to be monomeric with the typical three-legged piano- stool structure.
Original language | English |
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Pages (from-to) | 79-84 |
Number of pages | 6 |
Journal | Journal of Organometallic Chemistry |
Volume | 467 |
Issue number | 1 |
DOIs | |
Publication status | Published - 8 Mar 1994 |
Funding
Generous financial support from the Comunidad Autdnoma de Madrid (CAM C198/91) and the Uni-versidad de Alcall de Henares is gratefully acknowledged.
Funders | Funder number |
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Uni-versidad de Alcall de Henares | |
Comunidad Autónoma de Madrid | CAM C198/91 |
Keywords
- Amide
- Oxide
- Titanium
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
- Materials Chemistry