Abstract

AbstractTreatment of divalent (ONNO)V(TMEDA) (1; ONNO=[2,4‐Me2‐2‐(OH)C6H2CH2]2N(CH2)2NMe2) with CO2 afforded [(ONNO)V]2(μ‐OH)(μ‐formate) (2). Whereas the bridging hydroxo and formate groups both originated from CO2, the H atoms present on the two residues were obtained through H‐atom radical abstraction from the solvent. DFT calculations revealed an initially linear CO2 bonding mode, followed by deoxygenation, and highlighted a synergistic effect between the so‐formed oxo group and an additional bridging CO2 residue in promoting radical behavior.

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.