4.5 Article

Acid- and Base-Catalyzed Hydrolytic Hydrogen Evolution from Diboronic Acid

Journal

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
Volume 2021, Issue 29, Pages 3013-3018

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejic.202100093

Keywords

Acid catalysis; Base catalysis; Boron; Hydrogen evolution; Reaction mechanisms

Funding

  1. National Natural Science Foundation of China [21805166]
  2. 111 Project [D20015]
  3. Engineering Research Center of Eco-environment in Three Gorges Reservoir Region, Ministry of Education, China Three Gorges University [KF2019-05]
  4. outstanding young and middle-aged science and technology innovation teams, Ministry of Education, Hubei province, China [T2020004]
  5. Chinese Scientific Council
  6. Universite de Bordeaux
  7. Centre National de la Recherche Scientifique (CNRS)

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An efficient and simple method for producing H-2 and D-2 from acid- or base-catalyzed metal-free hydrolysis of B-2(OH)(4) has been developed, with the hydrogen atoms originating from water. This new catalytic system offers advantages such as high efficiency, simplicity of operation, sustainability, economy, and potential further use.
The efficient production of H-2 from hydrogen-rich sources, particularly from water, is a crucial task and a great challenge, both as a sustainable energy source and on the laboratory scale for hydrogenation reactions. Herein, a facile and effective synthesis of H-2 and D-2 from only acid- or base-catalyzed metal-free hydrolysis of B-2(OH)(4), a current borylation reagent, has been developed without any transition metal or ligand. Acid-catalyzed H-2 evolution was completed in 4 min, whereas the base-catalyzed process needed 6 min. The large kinetic isotopic effects for this reaction with D2O, deuteration experiments and mechanistic studies have confirmed that both H atoms of H-2 originate from water using either of these reactions. This new, metal-free catalytic system holds several advantages, such as high efficiency, simplicity of operation, sustainability, economy, and potential further use.

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