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.

We integrated theory with experiment to evaluate the catalytic cycle of seemingly incompatible steps enabled by nanowire array for CH4-to-CH3OH conversion, and determined the array’s efficacy in the context of microscopic compartmentalization.

The utilization of carbon dioxide in polymer synthesis is an attractive strategy for sustainable materials. Electrochemical CO 2 reduction would offer a natural starting point for producing monomers, but the conditions of electrocatalysis are often drastically different from the conditions of coordination−insertion polymerization. Reported here is a strategy for coupling electrochemical and organometallic catalysts that enables polyketone synthesis from CO 2 and ethylene in a single multicompartment reactor. Polyketone materials that are CO 2derived up to 50 wt % can be prepared in this way. Potentiostatic control over the CO-producing catalyst enables the controlled generation of low-pressure CO, which in conjunction with a palladium phosphine sulfonate organometallic catalyst enables copolymerization to nonalternating polyketones with the CO content tuned based on the applied current density.

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<p>Compartmentalization is a viable approach of ensuring the turnover of a solution cascade reaction with ephemeral intermediates, which may otherwise deactivate in the bulk solution. In biochemistry or enzyme-relevant cascade reactions, extensive models have been constructed to quantitatively analyze the efficacy of compartmentalization. Nonetheless, the application of compartmentalization and its quantitative analysis in non-biochemical reactions is seldomly performed, leaving much uncertainty about whether compartmentalization remains effective for non-biochemical, such as organometallic, cascade reactions. Here, we report our exemplary efficacy analysis of compartmentalization in our previously reported cascade reaction for ambient CH4-to-CH3OH conversion, mediated by O2-deactivating RhII metalloradical with O2 as the terminal oxidant in Si nanowire array electrode. We experimentally identified and quantified the productivity of key reaction intermediates, including RhII metalloradical and reactive oxygen species (ROS) from O2. We subsequently determined that the nanowire array enables about 81 % of the generated ephemeral intermediate in air, RhII metalloradical, to be utilized towards CH3OH formation, which is 0% in homogenous solution. Such an experimentally determined value was satisfactorily consistent with the results from our semi-quantitative kinetic model. The consistency suggests that the reported CH4-to-CH3OH conversion surprisingly possesses minimal unforeseen side reactions, and is favorably efficient as a compartmentalized cascade reaction. Our quantitative evaluation of the reaction efficacy offers design insights and caveats into application of nanomaterials to achieve a spatially controlled organometallic cascade reactions.</p>