Reactivity of a low-coordinate iron hydride complex

INOR 797

Ying Yu, Jeremy M. Smith, William W. Brennessel, and Patrick L. Holland, holland@chem.rochester.edu. Department of Chemistry, University of Rochester, Rochester, NY 14627
Transition metal hydride complexes have received considerable interest because of their participation in bond transformations as well as their extensive reactivity. We are particularly interested in low-coordinate iron hydrides, anticipating high reactivity due to the unsaturated metal center. Furthermore, biological interest in low-coordinate iron hydrides stems from both the growing evidence for low-coordinate iron atom in FeMoco and the proposed reactive metal hydride intermediates in the nitrogenase reduction cycle. Here we report the behavior of a low-coordinate iron hydride complex, [LMeFeH]2 (LMe = β-diketiminate ligand), and its reactions with nitrogenase substrates and different Lewis acids.

 

Organometallics
7:00 PM-10:00 PM, Tuesday, 12 September 2006 Moscone Center -- Hall D, Poster

Division of Inorganic Chemistry

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