Dihydrogen and silane addition to base-free, monomeric bis(cyclopentadienyl)titanium oxides |
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Authors: | Hanna Tamara E Lobkovsky Emil Chirik Paul J |
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Institution: | Department of Chemistry and Chemical Biology, Baker Laboratory, Cornell University, Ithaca, New York 14853, USA. |
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Abstract: | Synthesis of a family of monomeric, base-free bis(cyclopentadienyl)titanium oxide complexes, (eta5-C5Me4R)2Ti=O (R = iPr, SiMe3, SiMe2Ph), has been accomplished by deoxygenation of styrene oxide by the corresponding sandwich compound. One example, (eta5-C5Me4SiMe2Ph)2Ti=O, was characterized by X-ray diffraction. All three complexes undergo clean and facile hydrogenation at 23 degrees C, yielding the titanocene hydroxy hydride complexes (eta5-C5Me4R)2Ti(OH)H. For (eta5-C5Me4SiMe3)2Ti=O, the kinetics of hydrogenation were first-order in dihydrogen and exhibited a normal, primary kinetic isotope effect of 2.7(3) at 23 degrees C consistent with a 1,2-addition pathway. Isotope effects of the same direction but smaller magnitudes were determined for silane addition. |
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