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On the Mechanism of Hydrogen Activation by Frustrated Lewis Pairs
Author(s) -
Zeonjuk Lei Liu,
Vankova Nina,
Mavrandonakis Andreas,
Heine Thomas,
Röschenthaler GerdVolker,
Eicher Johannes
Publication year - 2013
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201302727
Subject(s) - frustrated lewis pair , lewis acids and bases , boranes , chemistry , catalysis , kinetics , computational chemistry , hydrogen , borane , thermodynamics , stereochemistry , organic chemistry , boron , physics , quantum mechanics
We report herein a comprehensive theoretical study of the thermodynamics and kinetics of molecular hydrogen activation by frustrated Lewis pairs (FLPs). A series of intermolecularly combined boranes (Lewis acids) and phosphines (Lewis bases), with experimentally established different reactivities towards H 2 , have been subjected to DFT and (SCS‐)MP2 calculations, and analyzed in terms of their structural properties, the energetics of association of the FLPs, and the kinetics of their interactions with H 2 and hydrogenation to the ion‐pair products. The analysis included the following steps: 1) assessment of the ability/inability of the Lewis species to preorganize into FLPs with an optimum arrangement of the acid and base sites for preconditioning the reaction with H 2 , 2) comprehension of the different thermodynamics of hydrogenation of the selected FLPs by comparing the Gibbs energies of the overall reactions, and 3) estimation of the mechanism of the activation of H 2 by identifying the reaction steps and the associated kinetic barriers. The results of our studies correlate well with experimental findings and have clarified the reasons for the observed different reactivities of the investigated systems, ranging from reversible or nonreversible activation to no reaction with H 2 . The derived predictions could assist the future design of Lewis acid–base systems with desired properties and applicability as metal‐free hydrogenation catalysts.