Names | |
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Preferred IUPAC name
Tetrakis(dimethylamino)titanium(IV) | |
Systematic IUPAC name
Dimethyl[tris(dimethylamino)titanio]amine | |
Other names
Titanium(IV) dimethylamide
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Identifiers | |
3D model (JSmol)
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Abbreviations | TDMAT |
ChemSpider | |
ECHA InfoCard | 100.019.914 |
EC Number |
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PubChem CID
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UN number | 2924 3398 |
CompTox Dashboard (EPA)
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Properties | |
C8H24N4Ti | |
Molar mass | 224.19 g/mol |
Appearance | yellow liquid |
Density | 0.947 g/cm3 |
Boiling point | 50 °C (122 °F; 323 K) at 0.05 mmHg |
reacts with water | |
Hazards | |
GHS labelling:[1] | |
Danger | |
H225, H260, H314 | |
P210, P223, P231+P232, P280, P303+P361+P353, P305+P351+P338 | |
NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tetrakis(dimethylamino)titanium (TDMAT), also known as Titanium(IV) dimethylamide, is a chemical compound. The compound is generally classified as a metalorganic species, meaning that its properties are strongly influenced by the organic ligands but the compound lacks metal-carbon bonds. It is used in chemical vapor deposition to prepare titanium nitride (TiN) surfaces and in atomic layer deposition as a titanium dioxide precursor. The prefix "tetrakis" refers the presence of four of the same ligand, in this case dimethylamides.
Preparation and properties
Tetrakis(dimethylamino)titanium is a conventional Ti(IV) compound in the sense that it is tetrahedral and diamagnetic. Unlike the many alkoxides, the diorganoamides of titanium are monomeric and thus at least somewhat volatile. It is prepared from titanium tetrachloride (which is also tetrahedral, diamagnetic, and volatile) by treatment with lithium dimethylamide:[2]
- TiCl4 + 4 LiNMe2 → Ti(NMe2)4 + 4 LiCl
Like many amido complexes, TDMAT is quite sensitive toward water, and its handling requires air-free techniques. The ultimate products of its hydrolysis is titanium dioxide and dimethylamine:
- Ti(NMe2)4 + 2 H2O → TiO2 + 4 HNMe2
In a related reaction, the compound undergoes exchange with other amines, evolving dimethylamine.
TMAT has been used in metalorganic chemical vapor deposition (MOCVD).[citation needed]
Related compounds
- Tetrakis(dimethylamido)vanadium (registry number 19824-56-7)
References
- ^ GHS: Sigma Aldrich 469858
- ^ D. C. Bradley and I. M. Thomas, "Part I. Metallo-organic Compounds containing Metal-Nitrogen bonds. Some Dialkylamino-derivatives of Titanium and Zirconium" J. Chem. Soc. 1960, 3857-3861. doi:10.1039/JR9600003857.