C-h bond activation by metal oxo compounds




















Metal-organic cooperative catalysis in C-H and C-C bond activation and its concurrent recovery. Direct sp3 C-H bond activation adjacent to nitrogen in heterocycles. Joining Europe PMC. Tools Tools overview. ORCID article claiming. Journal list. Grant finder. External links service. Annotations submission service.

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Contact us Helpdesk. Tech blog. Developer forum. Let us know how we are doing. Converting methane into more useful and readily transportable compounds has previously required the use of metal-based oxo catalysts, but now sulfur and phosphorus are showing their mettle. The growing concern for energy production with a small carbon footprint has greatly raised the profile of C—H bond activation.

A core problem of the field is the conversion of alkanes to any of a variety of more valuable functionalized products. As an example of an energy application, one such problem is the conversion of natural gas, methane, to a more readily transportable form such as methanol or ethane. Natural gas has a favourable carbon-to-hydrogen ratio relative to oil and coal and thus releases less carbon dioxide per unit energy output, but much natural gas is stranded at remote locations and cannot easily be transported to users because its boiling point is so low.

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Uranyl photochemistry with alkenes: Distinguishing between H-atom abstraction and electron transfer. Download references. The authors are grateful to D. Graham, I. Lamour, R. Mulvey and S. Robertson for help with obtaining the Raman spectroscopic measurements.

Polly L. You can also search for this author in PubMed Google Scholar. Correspondence to Polly L. Arnold or Jason B. Crystallographic data for compound 2thf CIF 50 kb. Crystallographic data for compound 3py CIF 91 kb. Crystallographic data for compound 4py CIF 68 kb.



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