4.8 Article

Unlocking the Potential of Substrate-Directed CO2Activation and Conversion: Pushing the Boundaries of Catalytic Cyclic Carbonate and Carbamate Formation

Journal

CHEMSUSCHEM
Volume 13, Issue 23, Pages 6056-6065

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.202002246

Keywords

carbon dioxide; cycloaddition; homogeneous catalysis; organic carbonates; substrate assistance

Funding

  1. CERCA Program/Generalitat de Catalunya
  2. ICREA
  3. Spanish MINECO [CTQ2017-88920-P]
  4. AGAUR [2017-SGR-232]
  5. European Community [889754, 840557]
  6. Marie Curie Actions (MSCA) [840557, 889754] Funding Source: Marie Curie Actions (MSCA)

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The unparalleled potential of substrate-induced reactivity modes in the catalytic conversion of carbon dioxide and alcohol or amine functionalized epoxides is discussed in relation to more conventional epoxide/CO(2)coupling strategies. This conceptually new approach allows for a substantial extension of the substitution degree and functionality of cyclic carbonate/carbamate products, which are predominant products in the area of nonreductive CO(2)transformations. Apart from the creation of an advanced library of CO2-based heterocyclic products and intermediates, also the underlying mechanistic reasons for this novel reactivity profile are debated with a prominent role for the design and structure of the involved catalysts.

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