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Solution Catalytic Cycle of Incompatible Steps for Ambient Air Oxidation of Methane to Methanol.
Natinsky, Benjamin S; Lu, Shengtao; Copeland, Emma D; Quintana, Jason C; Liu, Chong.
Afiliação
  • Natinsky BS; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90025, United States.
  • Lu S; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90025, United States.
  • Copeland ED; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90025, United States.
  • Quintana JC; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90025, United States.
  • Liu C; Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90025, United States.
ACS Cent Sci ; 5(9): 1584-1590, 2019 Sep 25.
Article em En | MEDLINE | ID: mdl-31572785
ABSTRACT
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 O2 and prevents catalytic air oxidation. We report selective oxidation of methane to methanol with an O2-sensitive metalloradical as the catalyst and air as the oxidant at room temperature and ambient pressure. The incompatibility between C-H activation and O2 oxidation is reconciled by electrochemistry and nanomaterials, with which a concentration gradient of O2 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 CH4 functionalization.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article