Transition metal mediated coupling of carbon dioxide and ethene to acrylic acid/acrylates

Manuela Hollering, Barnali Dutta, Fritz E. Kühn

Research output: Contribution to journalReview articlepeer-review

44 Scopus citations

Abstract

The search for renewable alternative energy sources and energy storing possibilities has gained significant importance during the last decades, due to depleting fossil carbon sources, the continuously increasing human population and a generally increasing interest in environmental issues. Carbon dioxide, for example, can be captured directly at its source and thus made available for chemical industry. Homogeneous catalysis in solution is an attractive alternative to established heterogeneous procedures to utilize the C1 building block CO2 as an abundant and cheap starting material. Therefore, the development of cost efficient routes to bulk chemicals like acrylic acid and acrylates has significant interest for industry. In order to progress more rapidly in such a research field a combination of experiment and computational calculations is often considered as beneficial. This review presents a comprehensive overview on the synthesis of acrylates and acrylic acid, starting from CO2, focusing on synthetic insights as well as current findings in theoretical studies. Mechanistic studies are outlined and rational approaches to a full catalytic cycle presented using various molecular transition metal catalysts. In addition, the first catalytic transformations of carbon dioxide and ethene to acrylic acid are presented.

Original languageEnglish
Pages (from-to)51-67
Number of pages17
JournalCoordination Chemistry Reviews
Volume309
DOIs
StatePublished - 15 Feb 2016

Keywords

  • Acrylic acid/acrylates
  • Carbon dioxide fixation
  • Density functional theory calculations
  • Ethene insertion
  • Homogeneous catalysis
  • Sustainable chemistry

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