Abstract
The Mo=PR2 π* orbital in a Mo phosphenium complex acts as acceptor in a new PIII -based Lewis superacid. This Lewis acid (LA) participates in electrophilic Si-H abstraction from E3 SiH to give a Mo-bound secondary phosphine ligand, Mo-PR2 H. The resulting Et3 Si+ ion remains associated with the Mo complex, stabilized by η1 -P-H donation, yet undergoes rapid exchange with an η1 -Si-H adduct of free silane in solution. The equilibrium between these two adducts presents an opportunity to assess the role of this new LA in catalytic reactions of silanes: is the LA acting as a catalyst or as an initiator? Preliminary results suggest that a cycle including the Mo-bound phosphine-silylium adduct dominates in the catalytic hydrosilylation of acetophenone, relative to a putative cycle involving the silane-silylium adduct or "free" silylium.
Sign-in/Register to access full text options 
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 callDisclaimer: 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.
