(Pentamethylcyclopentadienyl)titanium trichloride is an organotitanium compound with the formula Cp*TiCl3 (Cp* = C5(CH3)5). It is an orange solid. The compound adopts a piano stool geometry. An early synthesis involve the combination of lithium pentamethylcyclopentadienide and titanium tetrachloride.[2]
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Other names
Cp*TiCl3
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.152.688 |
PubChem CID
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UN number | 3261 |
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Properties | |
C10H15Cl3Ti | |
Molar mass | 289.45 g·mol−1 |
Appearance | Orange solid |
Melting point | 225 °C (437 °F; 498 K) |
Hazards | |
GHS labelling:[1] | |
Danger | |
H314 | |
P280, P305+P351+P338, P310 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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The compound is an intermediate in the synthesis of decamethyltitanocene dichloride. In the presence of organoaluminium compounds and other additives, it catalyzes the polymerization of alkenes.[3][4]
See also
editReferences
edit- ^ "Trichloro(pentamethylcyclopentadienyl)titanium(IV) 446289". Sigma-Aldrich.
- ^ King, R.B.; Bisnette, M.B. (1967). "Organometallic chemistry of the transition metals XXI. Some π-pentamethylcyclopentadienyl derivatives of various transition metals". Journal of Organometallic Chemistry. 8 (2): 287–297. doi:10.1016/S0022-328X(00)91042-8.
- ^ Ishihara, N.; Kuramoto, M.; Uoi, M. (1988). "Stereospecific polymerization of styrene giving the syndiotactic polymer". Macromolecules. 21 (12): 3356–3360. Bibcode:1988MaMol..21.3356I. doi:10.1021/ma00190a003.
- ^ Stephan, Douglas W.; Stewart, Jeffrey C.; Guérin, Frédéric; Courtenay, Silke; Kickham, James; Hollink, Emily; Beddie, Chad; Hoskin, Aaron; Graham, Todd; Wei, Pingrong; Spence, Rupert E. v. H.; Xu, Wei; Koch, Linda; Gao, Xiaoliang; Harrison, Daryll G. (2003). "An Approach to Catalyst Design: Cyclopentadienyl-Titanium Phosphinimide Complexes in Ethylene Polymerization". Organometallics. 22 (9): 1937–1947. doi:10.1021/om020954t.