Studies Relevent to Catalytic Activation Co & other small Molecules

Ford, Peter C.

University of California, Sant Barbara

关键词: Hydrocarbons;    Carbon Monoxide;    37 Inorganic, Organic, Physical And Analytical Chemistry;    Catalysts;    Spectroscopy;   

DOI  :  10.2172/839381
RP-ID  :  none
RP-ID  :  FG03-85ER13317
RP-ID  :  839381

美国|英语

来源: UNT Digital Library

【 摘 要 】

Detailed annual and triannual reports describing the progress accomplished during the tenure of this grant were filed with the Program Manager for Catalysis at the Office of Basic Energy Sciences. To avoid unnecessary duplication, the present report will provide a brief overview of the research areas that were sponsored by this grant and list the resulting publications and theses based on this DOE supported research. The scientific personnel participating in (and trained by) this grant's research are also listed. Research carried out under this DOE grant was largely concerned with the mechanisms of the homogeneous catalytic and photocatalytic activation of small molecules such as carbon monoxide, dihydrogen and various hydrocarbons. Much of the more recent effort has focused on the dynamics and mechanisms of reactions relevant to substrate carbonylations by homogeneous organometallic catalysts. A wide range of modern investigative techniques were employed, including quantitative fast reaction methodologies such as time-resolved optical (TRO) and time-resolved infrared (TRIR) spectroscopy and stopped flow kinetics. Although somewhat diverse, this research falls within the scope of the long-term objective of applying quantitative techniques to elucidate the dynamics and understand the principles of mechanisms relevant to the selective and efficient catalytic conversions of fundamental feedstocks to higher value materials.