Equilibria and kinetics in the CO-induced, reversible disproportionation of ((C5H5)2TiCl)2 to (C5H5)2TiCl2 and (C5H52Ti(CO)2. An IR study at elevated CO gas pressures

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1987
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van Raaij, Edith U.
Schmulbach, C. David
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Journal of Organometallic Chemistry. 1987, 328(3), pp. 275-285. ISSN 0022-328X. eISSN 1872-8561. Available under: doi: 10.1016/0022-328X(87)80245-0
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IR studies of toluene solutions of ((C5H5)2TiCl)2 under elevated CO pressures indicate the formation of a carbonyl complex, probably (C5H5)2Ti(CO)Cl, with ν(CO) 2068 cm. This species predominates at CO pressures above 100 bar, and is reasonably stable at temperatures around −30°C. At higher temperatures, disproportionation to (C5H5)2Ti(CO)2 and (C5H5)2TiCl2 occurs. This disproportionation is reversible; at +30°C and 1 bar of CO, roughly equal concentrations of ((C5H5)2TiCl)2 and of dicarbonyl and dichloride products are in equilibrium with each other. Practically complete formation of these products occurs at CO pressures above 10 bar. Rate laws and reaction mechanisms have been studied for the disproportionation reaction and for its reverse, the comproportionation of (C5H5)2Ti(CO)2 and (C5H5)2TiCl2 to ((C5H5)2TiCl)2, which predominates at lower CO pressures.

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ISO 690VAN RAAIJ, Edith U., C. David SCHMULBACH, Hans-Herbert BRINTZINGER, 1987. Equilibria and kinetics in the CO-induced, reversible disproportionation of ((C5H5)2TiCl)2 to (C5H5)2TiCl2 and (C5H52Ti(CO)2. An IR study at elevated CO gas pressures. In: Journal of Organometallic Chemistry. 1987, 328(3), pp. 275-285. ISSN 0022-328X. eISSN 1872-8561. Available under: doi: 10.1016/0022-328X(87)80245-0
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@article{vanRaaij1987Equil-24050,
  year={1987},
  doi={10.1016/0022-328X(87)80245-0},
  title={Equilibria and kinetics in the CO-induced, reversible disproportionation of ((C<sub>5</sub>H<sub>5</sub>)<sub>2</sub>TiCl)<sub>2</sub> to (C<sub>5</sub>H<sub>5</sub>)<sub>2</sub>TiCl<sub>2</sub> and (C<sub>5</sub>H<sub>52</sub>Ti(CO)<sub>2</sub>. An IR study at elevated CO gas pressures},
  number={3},
  volume={328},
  issn={0022-328X},
  journal={Journal of Organometallic Chemistry},
  pages={275--285},
  author={van Raaij, Edith U. and Schmulbach, C. David and Brintzinger, Hans-Herbert}
}
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    <dcterms:abstract xml:lang="eng">IR studies of toluene solutions of ((C&lt;sub&gt;5&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;TiCl)&lt;sub&gt;2&lt;/sub&gt; under elevated CO pressures indicate the formation of a carbonyl complex, probably (C&lt;sub&gt;5&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;Ti(CO)Cl, with ν(CO) 2068 cm&lt;sup&gt;−&lt;/sup&gt;. This species predominates at CO pressures above 100 bar, and is reasonably stable at temperatures around −30°C. At higher temperatures, disproportionation to (C&lt;sub&gt;5&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;Ti(CO)&lt;sub&gt;2&lt;/sub&gt; and (C&lt;sub&gt;5&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;TiCl&lt;sub&gt;2&lt;/sub&gt; occurs. This disproportionation is reversible; at +30°C and 1 bar of CO, roughly equal concentrations of ((C&lt;sub&gt;5&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;TiCl)&lt;sub&gt;2&lt;/sub&gt; and of dicarbonyl and dichloride products are in equilibrium with each other. Practically complete formation of these products occurs at CO pressures above 10 bar. Rate laws and reaction mechanisms have been studied for the disproportionation reaction and for its reverse, the comproportionation of (C&lt;sub&gt;5&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;Ti(CO)&lt;sub&gt;2&lt;/sub&gt; and (C&lt;sub&gt;5&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;TiCl&lt;sub&gt;2&lt;/sub&gt; to ((C&lt;sub&gt;5&lt;/sub&gt;H&lt;sub&gt;5&lt;/sub&gt;)&lt;sub&gt;2&lt;/sub&gt;TiCl)&lt;sub&gt;2&lt;/sub&gt;, which predominates at lower CO pressures.</dcterms:abstract>
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