Tris(acetylacetonato)titanium(III)
{{Chembox
|Name = Tris(acetylacetonato){{SHY}}titanium(III)
|ImageFile = Ti(acac)3.svg
|IUPACName = 4-oxopent-2-en-2-olate;titanium(3+)
|OtherNames = tris(2,4-pentanedionato)titanium, titanium trisacetylacetonate
|Section1={{Chembox Identifiers
|CASNo = 14284-96-9
|ChemSpiderID = 76066
|EC_number = 238-196-7
|PubChem = 84322
|StdInChI=1S/3C5H8O2.Ti/c3*1-4(6)3-5(2)7;/h3*3,6H,1-2H3;/q;;;+3/p-3
|StdInChIKey = SYIKXNDVCPYCLG-UHFFFAOYSA-K
|SMILES = CC(=CC(=O)C)[O-].CC(=CC(=O)C)[O-].CC(=CC(=O)C)[O-].[Ti+3]
}}
|Section2={{Chembox Properties
|C=15|H=21|O=6|Ti=1
|Appearance = blue solid
|Density = 1.366 g/cm3
}}
}}
Tris(acetylacetonato)titanium(III), often abbreviated Ti(acac)3, is a coordination complex of titanium(III) featuring acetylacetonate (acac) ligands, making it one of a family of metal acetylacetonates. It is a blue air-sensitive solid that dissolves in nonpolar organic solvents. The compound is prepared by treating titanium trichloride with acetylacetone in the presence of base.{{cite journal |doi=10.1007/s11224-016-0864-0|title=An Historic and Scientific Study of the Properties of Metal(III) Tris-acetylacetonates|year=2017|last1=Arslan|first1=Evrim|last2=Lalancette|first2=Roger A.|last3=Bernal|first3=Ivan|journal=Structural Chemistry|volume=28|pages=201–212|s2cid=99668641}} Being paramagnetic, it gives a contact-shifted proton NMR signal at 60 ppm upfield of TMS assigned to the methyl group.{{cite journal |doi=10.1021/ja01092a015|title=The Nuclear Magnetic Resonance of Some Paramagnetic Transition Metal Acetylacetonates|year=1965|last1=Eaton|first1=D. R.|journal=Journal of the American Chemical Society|volume=87|issue=14|pages=3097–3102}}
Structure
It is an octahedral complex. The Ti-O bonds lengths range from 2.023 to 2.013 Å, the large variation being attributed to the Jahn-Teller effect. Ti(acac)3 possesses helical chirality, giving rise to Δ- and Λ-enantiomers.
It is a precatalyst for Ziegler-Natta catalysis.{{cite journal |doi=10.1021/ma00195a021|title=Soluble Catalysts for Syndiotactic Polymerization of Styrene|year=1989|last1= Zambelli|first1=Adolfo|last2=Oliva|first2=Leone|last3=Pellecchia|first3 =Claudio|journal=Macromolecules|volume=22|issue=5|pages=2129–2130|bibcode=1989MaMol..22.2129Z}}