Reactivity Models of Hydrogen Activation by Frustrated Lewis Pairs: Synergistic Electron Transfers or Polarization by Electric Field?

2013 ◽  
Vol 135 (11) ◽  
pp. 4425-4437 ◽  
Author(s):  
Tibor András Rokob ◽  
Imre Bakó ◽  
András Stirling ◽  
Andrea Hamza ◽  
Imre Pápai
Synthesis ◽  
2021 ◽  
Author(s):  
Felix Wech ◽  
Urs Gellrich

In recent years, borane-based frustrated Lewis pairs proved to be efficient hydrogenation catalysts and became an alternative to transition metal-based systems. The hydrogen activation by classic FLPs leads to a protonated Lewis base and a borohydride. Consequently, hydrogenations catalyzed by classic FLPs consist of stepwise hydride transfer reactions and protonations (or vice versa). More recently, systems that operate via an initial hydroboration have allowed extending the substrate scope for FLP catalyzed hydrogenations. Within this review, hydrogenations of organic substrates catalyzed by borane-based frustrated Lewis pairs are discussed. Emphasis is given to the mechanistic aspects of these catalytic reactions.


2013 ◽  
Vol 19 (51) ◽  
pp. 17413-17424 ◽  
Author(s):  
Lei Liu Zeonjuk ◽  
Nina Vankova ◽  
Andreas Mavrandonakis ◽  
Thomas Heine ◽  
Gerd‐Volker Röschenthaler ◽  
...  

2015 ◽  
Vol 17 (16) ◽  
pp. 10715-10725 ◽  
Author(s):  
Patricia Pérez ◽  
Diana Yepes ◽  
Pablo Jaque ◽  
Eduardo Chamorro ◽  
Luis R. Domingo ◽  
...  

The activation of molecular hydrogen, H2, by three models of FLPs.


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