Di(tert-butyl) amido titanium transition metal complexes

INOR 169

Charles W. Spicer and Gregory S. Girolami, girolami@scs.uiuc.edu. School of Chemical Sciences, University of Illinois at Urbana-Champaign, 600 South Mathews Avenue, Urbana, IL 61801
Transition metal compounds with low coordination numbers often exhibit interesting structural and chemical properties. The bulky and little studied di(tert-butyl)amide ligand is well suited for making compounds that exhibit such properties. Treatment of TiCl4 with HN(t-Bu)2 affords the chloride-bridged dimer Ti2Cl6[N(t-Bu)2]2; each five-coordinate titanium atom is involved with one close Ti∙∙∙C contact of 2.63 Å with a g-carbon atom. Treatment of TiCl4 with LiN(t-Bu)2 affords the imide-bridged dimer Ti2Cl2[N(t-Bu)]2[N(t-Bu)2]2, in which the bridging imide group appears to be the result of dealkylation of the di(tert-butyl)amide ligand. Variable temperature NMR studies reveal that rotation about the Ti-N bonds is slow on the NMR time scale at low temperature. The nature of the agnostic interactions will be discussed.

 

Coordination Chemistry: Synthesis
7:00 PM-10:00 PM, Sunday, 10 September 2006 Moscone Center -- Hall D, Poster

Sci-Mix
8:00 PM-10:00 PM, Monday, 11 September 2006 Moscone Center -- Hall D, Sci-Mix

Division of Inorganic Chemistry

The 232nd ACS National Meeting, San Francisco, CA, September 10-14, 2006