Abstract

The utilization of CO2 to generate chemical fuels, such as formic acid, is a potentially beneficial route to balance carbon emissions and reduce dependence on fossil fuels. The development of efficient catalysts for CO2 hydrogenation is needed to implement this fuel generation. In the molecular catalyst design presented here, we covalently attached a rhodium complex, ([RhI(PNglyP)2]−, where PNglyP is defined as PEt2–CH2–N(CH2CO2–)–CH2–PEt2) to a protein scaffold, (lactococcal multidrug resistant regulator from Lactococcus lactis) to use the protein environment around the metal center to control substrate delivery and therefore enable and improve catalytic activity. The reactivities of the rhodium complex and the synthetic metalloenzyme were characterized by high-pressure operando NMR techniques. In solution, the rhodium complex alone is not a catalyst for CO2 hydrogenation. Incorporation of the rhodium complex into the protein scaffold resulted in a gain of function, turning on CO2 hydrogenation activity....

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.