4.8 Article

Aluminum Metal-Organic Framework-Ligated Single-Site Nickel(II)-Hydride for Heterogeneous Chemoselective Catalysis

Journal

ACS CATALYSIS
Volume 11, Issue 7, Pages 3943-3957

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.0c04379

Keywords

nickel-hydride catalyst; metal-organic frameworks; hydrogenation; hydrogenolysis; chemoselectivity

Funding

  1. Science and Engineering Research Board (SERB), India [ECR/2017/001931]
  2. CSIR
  3. UGC

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The study introduces a highly efficient, chemoselective, and reusable nickel hydride catalyst for hydrogenation of nitro and nitrile compounds under mild conditions. The catalyst, based on aluminum metal-organic frameworks, has broad substrate scope and excellent functional group tolerance, and can be recycled at least 10 times. This work highlights the potential of MOF-based single-site earth-abundant metal catalysts for practical and eco-friendly production of chemical feedstocks and biofuels.
The development of chemoselective and heterogeneous earth-abundant metal catalysts is essential for environmentally friendly chemical synthesis. We report a highly efficient, chemoselective, and reusable single-site nickel(II) hydride catalyst based on robust and porous aluminum metal-organic frameworks (MOFs) (DUT-5) for hydrogenation of nitro and nitrile compounds to the corresponding amines and hydrogenolysis of aryl ethers under mild conditions. The nickel-hydride catalyst was prepared by the metalation of aluminum hydroxide secondary building units (SBUs) of DUT-5 having the formula of Al(mu(2)-OH)(bpdc) (bpdc = 4,4'-biphenyldicarboxylate) with NiBr2 followed by a reaction with NaEt3BH. DUT-5-NiH has a broad substrate scope with excellent functional group tolerance in the hydrogenation of aromatic and aliphatic nitro and nitrile compounds under 1 bar H-2 and could be recycled and reused at least 10 times. By changing the reaction conditions of the hydrogenation of nitriles, symmetric or unsymmetric secondary amines were also afforded selectively. The experimental and computational studies suggested reversible nitrile coordination to nickel followed by 1,2-insertion of coordinated nitrile into the nickel-hydride bond occurring in the turnover-limiting step. In addition, DUT-5-NiH is also an active catalyst for chemoselective hydrogenolysis of carbon-oxygen bonds in aryl ethers to afford hydrocarbons under atmospheric hydrogen in the absence of any base, which is important for the generation of fuels from biomass. This work highlights the potential of MOF-based single-site earth-abundant metal catalysts for practical and eco-friendly production of chemical feedstocks and biofuels.

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