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Dive into the research topics where Raymond A. Cook is active.

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Featured researches published by Raymond A. Cook.


Chemical Communications | 2002

Supported ionic liquid catalysis investigated for hydrogenation reactions

Christian P. Mehnert; Edmund J. Mozeleski; Raymond A. Cook

The concept of supported ionic liquid catalysis (silc) has successfully been applied to hydrogenation reactions, which significantly reduced the required amounts of ionic liquid phase and enabled the usage of fixed-bed technology; the resulting catalysts exhibited high activity and outstanding stability.


Chemical Communications | 2002

Preparation of C9-aldehyde via aldol condensation reactions in ionic liquid media

Christian P. Mehnert; Nicholas C. Dispenziere; Raymond A. Cook

C9-aldehyde has been prepared via aldol condensation reactions in ionic liquid media; catalyst investigation showed enhanced product selectivity for the desired aldehyde in ionic liquid media than in conventional solvent systems.


Catalysis Letters | 2002

13C NMR study of the acid-catalyzed carbonylation of methyl tert-butyl ether (MTBE)

Ned C. Haubein; Linda J. Broadbelt; Edmund J. Mozeleski; Richard H. Schlosberg; Raymond A. Cook; Christian P. Mehnert; Dan Fărcaşiu

Methyl tert-butyl ether (MTBE) is a widely used additive in oxygenated gasoline that has recently been identified as a potential health threat to the drinking water supply due to leaking underground storage tanks. One alternate use for MTBE is the production of methyl 2,2-dimethylpropanoate (methyl pivalate) via Koch carbonylation chemistry. BF3/H2O catalysts are employed in industrial applications of Koch chemistry, but cannot be used for direct ester production because the presence of water in the system leads to the formation of carboxylic acids and lowers the selectivity to esters. Therefore, a BF3/CH3OH complex was investigated for the carbonylation of MTBE to avoid this loss in selectivity. This study used 13C NMR spectroscopy and ab initio calculations to investigate this carbonylation reaction. NMR results and ab initio calculations suggest a structure for the BF3/CH3OH acid which is in agreement with previous studies, and a Hammett acidity value of -4.2 was calculated for BF3-2.19CH3OH using the Δδ method. It is believed that these are the first reported ab initio calculations on the BF3/CH3OH system. NMR results also show that MTBE begins to react between 50 °C and 75 °C to produce oligomers of isobutene when no CO is present and carbonylated species when CO is present.


Journal of the American Chemical Society | 2002

Supported Ionic Liquid Catalysis − A New Concept for Homogeneous Hydroformylation Catalysis

Christian P. Mehnert; Raymond A. Cook; Nicholas C. Dispenziere; Mobae Afeworki


Journal of the American Chemical Society | 1998

Molecular Engineering in Homogeneous Catalysis: One-Phase Catalysis Coupled with Biphase Catalyst Separation. The Fluorous-Soluble HRh(CO){P[CH2CH2(CF2)5CF3]3}3 Hydroformylation System

István T. Horváth; Gabor Kiss; Raymond A. Cook; Jeffrey E. Bond; Paul A. Stevens; József Rábai; Edmund J. Mozeleski


Polyhedron | 2004

Biphasic hydroformylation catalysis in ionic liquid media

Christian P. Mehnert; Raymond A. Cook; Nicholas C. Dispenziere; Edmund J. Mozeleski


Organometallics | 1993

Low-temperature methane chlorination with aqueous platinum chlorides in the presence of chlorine

István T. Horváth; Raymond A. Cook; John M. Millar; Gabor Kiss


Archive | 1995

Direct hydroformylation of a multi-component synthesis gas containing carbon monoxide, hydrogen, ethylene, and acetylene

Gabor Kiss; Frank Hershkowitz; Harry W. Deckman; Michael Gerard Matturro; István T. Horváth; Anthony M. Dean; Raymond A. Cook


Archive | 2002

Method for preparing high-purity ionic liquids

Christian P. Mehnert; Nicholas C. Dispenziere; Raymond A. Cook


Archive | 2001

Ionic liquid compositions

Christian P. Mehnert; Raymond A. Cook

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