5 years ago

Dynamic Interconversion between Boroxine Cages Based on Pyridine Ligation

Dynamic Interconversion between Boroxine Cages Based on Pyridine Ligation
Nobuharu Iwasawa, Nobuhiro Yasuda, Shunsuke Shimo, Hidehiro Uekusa, Kosuke Ono, Kohei Takahashi
The dynamic interconversion of large covalent organic cages was achieved simply by heating or acid/base treatment. In their Communication (DOI: 10.1002/anie.201713221), N. Iwasawa and co-workers show that a mixture of the boroxine cages 12-mer and 15-mer was cleanly converted into a pyridine adduct of the boroxine cage 9-mer upon treatment with pyridine, and the geometry of N-coordinated boron atoms changed from trigonal to tetrahedral. This is the first covalent organic cage molecule that undergoes a reversible transformation between different cage structures.

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

DOI: 10.1002/anie.201801720

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.