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Cationic Cobalt (Ii) Hydroformylation, Drew Michael Hood
Cationic Cobalt (Ii) Hydroformylation, Drew Michael Hood
LSU Doctoral Dissertations
While investigating a bimetallic cobalt hydroformylation catalyst a new class of monometallic cationic cobalt (II) hydroformylation catalyst were discovered. These newly discovered catalyst proved to be very unique with high hydroformylation activity under mild conditions. The pre-catalyst were characterized using various methods including NMR, EPR, MS, and X-ray crystallography. Similarly the active catalyst was also investigated using NMR, EPR, FTIR, and X-ray crystallography. Various catalyst modifications were investigated for their effects on hydroformylation activity. Likewise various reaction parameters were probed to determine their effect on hydroformylation activity. Finally the best cationic cobalt (II) catalyst were directly compared to industry standards …
Investigating Cationic Metal Centers For Hydroformylation, Ryan Alexander Johnson
Investigating Cationic Metal Centers For Hydroformylation, Ryan Alexander Johnson
LSU Doctoral Dissertations
Bimetallic cooperativity can potentially increase activity of reactions. This concept is another way to increase reactivity besides simply focusing on the steric and electronic effects of a ligand. A binucleating tetrasphosphine ligand has been developed to showcase bimetallic cooperativity between two rhodium metal centers. Hydroformylation is a widely used industrial process to produce aldehydes from alkenes, H2, and CO. The dirhodium catalyst, [Rh2(μ-CO)(CO)3(rac-et,ph-P4-Ph)](BF4)2,is highly active leading to favorable results when using a DMF/water solvent system, 1-hexene, 90 psi 1:1 H2/CO, and 90° C: initial turnover frequency …