Cargando…

Solution Catalytic Cycle of Incompatible Steps for Ambient Air Oxidation of Methane to Methanol

[Image: see text] Direct chemical synthesis from methane and air under ambient conditions is attractive yet challenging. Low-valent organometallic compounds are known to activate methane, but their electron-rich nature seems incompatible with O(2) and prevents catalytic air oxidation. We report sele...

Descripción completa

Detalles Bibliográficos
Autores principales: Natinsky, Benjamin S., Lu, Shengtao, Copeland, Emma D., Quintana, Jason C., Liu, Chong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764157/
https://www.ncbi.nlm.nih.gov/pubmed/31572785
http://dx.doi.org/10.1021/acscentsci.9b00625
Descripción
Sumario:[Image: see text] Direct chemical synthesis from methane and air under ambient conditions is attractive yet challenging. Low-valent organometallic compounds are known to activate methane, but their electron-rich nature seems incompatible with O(2) and prevents catalytic air oxidation. We report selective oxidation of methane to methanol with an O(2)-sensitive metalloradical as the catalyst and air as the oxidant at room temperature and ambient pressure. The incompatibility between C–H activation and O(2) oxidation is reconciled by electrochemistry and nanomaterials, with which a concentration gradient of O(2) within the nanowire array spatially segregated incompatible steps in the catalytic cycle. An unexpected 220 000-fold increase of the apparent reaction rate constants within the nanowire array leads to a turnover number up to 52 000 within 24 h. The synergy between nanomaterials and organometallic chemistry warrants a new catalytic route for CH(4) functionalization.