4.8 Article

In Situ Formation of Frustrated Lewis Pairs in a Water-Tolerant Metal-Organic Framework for the Transformation of CO2

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 58, Issue 16, Pages 5371-5375

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201901171

Keywords

CO2 conversion; frustrated Lewis pairs; heterogeneous catalysis; metal-organic frameworks; sustainable chemistry

Funding

  1. EPFL
  2. Swiss National Science Foundation (SNSF) [PZENP2166888]
  3. National Center of Competence in Research (NCCR), Materials' Revolution: Computational Design and Discovery of Novel Materials (MARVEL) of the SNSF

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Frustrated Lewis pairs (FLPs) consist of sterically hindered Lewis acids and Lewis bases, which provide high catalytic activity towards non-metal-mediated activation of inert small molecules, including CO2 among others. One critical issue of homogeneous FLPs, however, is their instability upon recycling, leading to catalytic deactivation. Herein, we provide a solution to this issue by incorporating a bulky Lewis acid-functionalized ligand into a water-tolerant metal-organic framework (MOF), named SION-105, and employing Lewis basic diamine substrates for the in situ formation of FLPs within the MOE Using CO2 as a C1-feedstock, this combination allows for the efficient transformation of a variety of diamine substrates into benzimidazoles. SION-105 can be easily recycled by washing with MeOH and reused multiple times without losing its identity and catalytic activity, highlighting the advantage of the MOF approach in FLP chemistry.

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