5 years ago

New Motifs in Deoxydehydration: Beyond the Realms of Rhenium

New Motifs in Deoxydehydration: Beyond the Realms of Rhenium
Allan R. Petersen, Peter Fristrup
The deoxydehydration (DODH) reaction remains one of the most efficient methods of reducing the oxygen content of biomass while keeping important functionality in place. This reaction is traditionally catalysed by high-valent oxo-rhenium species. Recent research into heterogeneous rhenium-based catalysts for DODH demonstrates their ability to rival and in some cases surpass their homogeneous counterparts. Furthermore, catalysts based on the metals molybdenum and vanadium show great potential as inexpensive alternatives to rhenium catalysts. In this Minireview, we detail the recent developments within the field of DODH with particular emphasis on discoveries outside the realms of rhenium. To rhenium and beyond: Recent developments within the field of deoxydehydration are reviewed. The focus is on novel heterogeneous catalysts as well as the discovery of non-rhenium catalysts. The key aspects in the deoxydehydration reaction that lead to an ongoing discussion into its mechanism are also highlighted.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/chem.201701153

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.