Catalytic reduction of polar substrates without metals: A thermodynamic and kinetic study of heterolytic activation of hydrogen by vacancies in frustrated Lewis pairs

PBCatH2, ΔH ca. −43(4) kJ/mol. Solution phase 19F nuclear magnetic resonance spectroscopy was used to determine the rate of heterolytic splitting of H2 by PBCat, k = 0.7(.3) M−1 s−1 and the equilibrium constant for PBCat + H2(soln) ⇔ PBCatH2, Keq(295) = 2.2(.5) × 105 M, providing an estimate of the free energy for heterolytic splitting of H2, ΔG ca. −29.8(1.3) kJ/mol at 295 K in toluene. Deconvolution of the instrument time constant from the heat flux using the Tian equation shows the concentration of imine decreases linearly in time (i.e., the substrate imine is not involved in the rate limiting step, suggesting that H2 activation by the Lewis acid-base pair is rate limiting). -->
ISSN: 0920-5861
Přístupová URL adresa: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43d631f89275a7f9a56d5bfa1147e3da
https://doi.org/10.1016/j.cattod.2014.10.040
Rights: OPEN
Přírůstkové číslo: edsair.doi.dedup.....43d631f89275a7f9a56d5bfa1147e3da
Autor: Gary Edvenson, Sean M. Whittemore, Kshitij Parab, Abhi Karkamkar, Doinita Neiner, Tom Autrey, Donald M. Camaioni
Rok vydání: 2015
Předmět:
Zdroj: Catalysis Today. 251:28-33
ISSN: 0920-5861
Popis: Time-resolved reaction calorimetry provides a measure of the turnover frequency (TOF), ca. 1.1 min−1, and enthalpic driving force, ca. −73 kJ/mol, for the metal-free catalytic reduction of an organic imine, tert-butylbenzaldimine, (tBu-IM) with a frustrated Lewis acid-base pair, [2-(dimesitylphosphino)ethyl] bis(pentafluorophenyl)borane (PBCat), at 298 K and 13.8 bar hydrogen (H2) pressure. Lowering the H2 pressure by a factor of two decreases the TOF (0.6 min−1), which is consistent with a pseudo first-order reaction in H2. In the absence of imine, the heat flux measured in the calorimeter provides a measure of the enthalpy for heterolytic splitting of H2, PBcat + H2 --> PBCatH2, ΔH ca. −43(4) kJ/mol. Solution phase 19F nuclear magnetic resonance spectroscopy was used to determine the rate of heterolytic splitting of H2 by PBCat, k = 0.7(.3) M−1 s−1 and the equilibrium constant for PBCat + H2(soln) ⇔ PBCatH2, Keq(295) = 2.2(.5) × 105 M, providing an estimate of the free energy for heterolytic splitting of H2, ΔG ca. −29.8(1.3) kJ/mol at 295 K in toluene. Deconvolution of the instrument time constant from the heat flux using the Tian equation shows the concentration of imine decreases linearly in time (i.e., the substrate imine is not involved in the rate limiting step, suggesting that H2 activation by the Lewis acid-base pair is rate limiting).
Databáze: OpenAIRE
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