A series of Group 7 organometallic noble gas complexes, (η5-C5R5)M(CO)2L (M = Mn and Re; R = H, Me, and Et (Mn only); L = Kr and Xe) have been characterized in supercritical noble gas solution at room temperature using fast time-resolved infrared spectroscopy. The kinetics and activation parameters for the reaction of these complexes with CO were measured and compared to the analogous alkane complexes, (η5-C5H5)M(CO)2(n-heptane) (M = Mn and Re). Evidence obtained from values of the activation enthalpies and experiments, in which the lifetimes of (η5-C5R5)Mn(CO)2Xe (R = H, Me, and Et) were measured as a function of [CO] at a constant [CO]/[Xe] ratio, suggests that the reaction of the noble gas complexes with CO occurs mainly via a dissociative or dissociative interchange mechanism.
|Number of pages||8|
|Journal||Journal of Physical Chemistry A|
|Publication status||Published - May 11 2000|
ASJC Scopus subject areas
- Physical and Theoretical Chemistry