Titanocene dicarbonyl

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Titanocene dicarbonyl
Dicarbonylbis(cyclopentadienyl)titanium
Space-filling model of the titanocene dicarbonyl molecule
Names
IUPAC name
dicarbonylbis (η5- cyclopentadienyl) titanium
Other names
Dicarbonyldi- π-cyclopentadienyltitanium
Dicarbonylbis (η5- cyclopentadienyl) titanium(II)
Identifiers
12129-51-0 YesY
Properties
C12H10O2Ti
Molar mass 234.09 g/mol
Appearance maroon solid pyrophoric
Melting point 90 °C (194 °F; 363 K)
Boiling point Sublimes at 40 to 80 °C (104 to 176 °F; 313 to 353 K) at 0.001 mmHg
insoluble
Solubility in other solvents THF, benzene
Structure
tetrahedral
Hazards
Main hazards flammable
Related compounds
Related compounds
Cp2TiCl2
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
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Infobox references

Dicarbonylbis(cyclopentadienyl)titanium is the chemical compound with the formula (η5-C5H5)2Ti(CO)2, abbreviated Cp2Ti(CO)2. This maroon-coloured, air-sensitive species is soluble in aliphatic and aromatic solvents.[1] It has been used for the deoxygenation of sulfoxides, reductive coupling of aromatic aldehydes and reduction of aldehydes.

Structure and synthesis[edit]

Cp2Ti(CO)2 is prepared via the reduction of titanocene dichloride with magnesium under an atmosphere of carbon monoxide.[2]

(C5H5)2TiCl2 + Mg + 2 CO → (C5H5)2Ti(CO)2 + MgCl2

Both Cp2Ti(CO)2 and Cp2TiCl2 are tetrahedral as are related zirconium and hafnium compounds.

References[edit]

  1. ^ Sikora, D.J.; Moriarty, K.J.; Rausch, M.D. (1990). "Reagents for Transition Metal complex and Organometallic syntheses." Inorganic Sytheses. 28. pp. 250-251.
  2. ^ "Dicarbonylbis(cyclopentadienyl)titanium". Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons, Ltd. 2001. doi:10.1002/047084289X.rd073.