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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.
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Heterogeneous Epoxide Carbonylation by Cooperative Ion-Pair Catalysis in Co(CO) 4 – -Incorporated Cr-MIL-101
Not Available
Mechanism of Electrocatalytic H 2 Evolution, Carbonyl Hydrogenation, and Carbon–Carbon Coupling on Cu
Not Available
Discovery of the HCV NS3/4A Protease Inhibitor (1R,5S)-N-[3-Amino-1-(cyclobutylmethyl)-2,3-dioxopropyl]-3-[2(S)-[[[(1,1-dimethylethyl)amino]carbonyl]amino]-3,3-dimethyl-1-oxobutyl]-6,6-dimethyl-3-azabicyclo[3.1.0]hexan-2(S)-carboxamide (Sch 503034) II. Key Steps in Structure-Based Optimization
Abstract not provided
Discovery of (1R,5S)-N-[3-Amino-1-(cyclobutylmethyl)-2,3-dioxopropyl]- 3-[2(S)-[[[(1,1-dimethylethyl)amino]carbonyl]amino]-3,3-dimethyl-1-oxobutyl]- 6,6-dimethyl-3-azabicyclo[3.1.0]hexan-2(S)-carboxamide (SCH 503034), a Selective, Potent, Orally Bioavailable Hepatitis C Virus NS3 Protease Inhibitor: A Potential Therapeutic Agent for the Treatment of Hepatitis C Infection
Abstract not provided
Rapid and ordered carbonylation and oxygenation of a cobalt(II) methyl
To M CoMe reacts rapidly with CO to give a low spin To M Co{C(O)Me}CO species, which is selectively oxygenated to form To M CoOAc.
A cyanide-bridged di-manganese carbonyl complex that photochemically reduces CO 2 to CO
Manganese(I) tricarbonyl complexes such as [Mn(bpy)(CO) 3 L] (L = Br, or CN) are known to be electrocatalysts for CO 2 reduction to CO. However, due to their rapid photodegradation under UV and visible light, these monomeric manganese complexes have not been considered as photocatalysts for CO 2 reduction without the use of a photosensitizer. We report a cyanide-bridged di-manganese complex, {[Mn(bpy)(CO) 3 ] 2 (μ-CN)}ClO 4 , which is both electrocatalytic and photochemically active for CO 2 reduction to CO. Compared to the [Mn(bpy)(CO) 3 CN] electrocatalyst, our CN-bridged binuclear complex is a more efficient electrocatalyst for CO 2 reduction using H 2 O as a proton source. In addition, we report a photochemical CO 2 reduction to CO using the dimanganese complex under 395 nm irradiation.