(Cyclopentadienyl)titanium trichloride
Jump to navigation
Jump to search
| |
| Names | |
|---|---|
| Other names
Titanocene trichloride
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
| ECHA InfoCard | 100.156.156 |
PubChem CID
|
|
| UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| C5H5Cl3Ti | |
| Molar mass | 219.31 g·mol−1 |
| Appearance | orange solid |
| Density | 1.768 g/cm3 |
| Melting point | 210 °C (410 °F; 483 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
(Cyclopentadienyl)titanium trichloride is an organotitanium compound with the formula (C5H5)TiCl3. It is a moisture sensitive orange solid. The compound adopts a piano stool geometry.[1]
Preparation and reactions
[edit](C5H5)TiCl3 is prepared by the reaction of titanocene dichloride and titanium tetrachloride:
- (C5H5)2TiCl2 + TiCl4 → 2 (C5H5)TiCl3
The complex is electrophilic, readily forming alkoxide complexes upon treatment with alcohols.[2]
Reduction of (cyclopentadienyl)titanium trichloride with zinc powder gives the polymeric Ti(III) derivative (cyclopentadienyl)titanium dichloride:[3]
- (C5H5)TiCl3 + 0.5 Zn → 1/n [(C5H5)TiCl2]n + ZnCl2
A related reduction can be effected with cobaltocene:[4]
- (C5H5)TiCl3 + (C5H5)2Co → [(C5H5)2Co]+[(C5H5)TiCl3]−
Other evidence for the Lewis acidity of the trichloride is the ready formation of adducts with phosphine ligands:[5]
- (C5H5)TiCl3 + P(CH3)3 → (C5H5)TiCl3(P(CH3)3
See also
[edit]- (Cyclopentadienyl)zirconium trichloride
- (Pentamethylcyclopentadienyl)titanium trichloride
- (Indenyl)titanium trichloride[6]
References
[edit]- ^ Rossini, A. J.; Mills, R. W.; Briscoe, G. A.; Norton, E. L.; et al. (2009). "Solid-State Chlorine NMR of Group IV Transition Metal Organometallic Complexes". Journal of the American Chemical Society. 131 (9): 3317–3330. doi:10.1021/ja808390a. PMID 19256569.
- ^ Andreas Hafner; Rudolf O. Duthaler (2001). "Trichloro(cyclopentadienyl)titanium". EEROS. doi:10.1002/047084289X.rt202m. ISBN 0-471-93623-5.
- ^ Lucas, C. R.; Green, M. L. H. (2007) [1976]. "Some η-Cyclopentadienyl Complexes of Titanium(III)". Inorganic Syntheses. Vol. 16. pp. 237–240. doi:10.1002/9780470132470.ch62. ISBN 978-0-470-13178-7.
- ^ Hughes, D.L.; Jimenez-Tenorio, M.; Leigh, G.J. (1989). "Synthesis of [Co(η5-C5H5)2][M(η5-C5H5)Cl3] salts (M = Ti or V): Crystal structure of [Co(η5-C5H5)2][Tc(η5-C5H5)Cl3]". Polyhedron. 8 (13–14): 1780–1781. doi:10.1016/S0277-5387(00)80641-5.
- ^ Nadasdi, T. Timothy; Stephan, Douglas W. (1993). "Radical Routes to Titanium(IV) Thiolate Complexes: Structure and Reactivity of ((η5--C5H5)TiIII and -TiIV Donor and Thiolate Derivatives". Inorganic Chemistry. 32 (26): 5933–5938. doi:10.1021/ic00078a008.
- ^ Morris, Robert J.; Shaw, Scott L.; Jefferis, Jesse M.; Storhoff, James J.; Goedde, Dean M. (1998). "Monoindenyltrichloride Complexes of Titanium(IV), Zirconium(IV), and Hafnium(IV)". Inorganic Syntheses. Vol. 32. pp. 215–221. doi:10.1002/9780470132630.ch36. ISBN 978-0-471-24921-4.