Received March 9, 2006

Abstract:

Ti-TEMPO (TEMPO = 2,2,6,6-tetramethylpiperidine-N-oxyl) provides a means for generating Ti(III) complexes by homolysis of the Ti-O bond. It has been determined that bis-Cp-Ti-TEMPO complexes readily undergo homolytic cleavage while the mono-Cp-Ti-TEMPO complexes do not. Here Ti K- and Cl K-edge XAS are applied to directly determine the oxidation state of TiCl₃TEMPO, TiCpCl₂TEMPO, and TiCp₂ClTEMPO, with reference to Ti(III) and Ti(IV) complexes of known oxidation state. The Ti K-edge data show that Ti(III) complexes exhibit a pre-edge feature ~1 eV lower than any of the Ti(IV) complexes; while the Cl K-edges show that Ti(III) complexes have a Cl K- pre-edge feature to ~1 eV higher energy than any of the Ti(IV) complexes. Taken together, the Ti and Cl K-edge data indicate that the Ti-TEMPO complexes are best described as Ti(IV)-TEMPO anions (rather than Ti(III)-nitroxyl radicals). In addition, the Cl K-edges indicate that replacement of Cl by Cp weakens the bonding with the remaining ligands, with the Cl 3p covalency decreasing from 25% to 21% to 17% on going from TiCl₃TEMPO to TiCpCl₂TEMPO to TiCp₂ClTEMPO. DFT calculations also show that the electronic structures of the Ti-TEMPO complexes are modulated by the replacement of chloride by Cp. The effect of the Cp on the ancillary ligation is one factor that contributes to facile Ti-O bond homolysis in TiCp₂ClTEMPO. However, the results indicate the primary contribution to the energetics of Ti-O bond homolysis in TiCp₂ClTEMPO is stabilization of the three-coordinate product by Cp.

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