Add like
Add dislike
Add to saved papers

A zwitterionic hydrocarbon-soluble borenium ion based on a β-diketiminate backbone.

A versatile synthetic route has been developed to access strongly Lewis acidic borenium cations (and heavier group 13 analogues) featuring a pendant weakly-coordinating borate function. The hydrocarbon-soluble borenium/borate zwitterion is more strongly Lewis acidic than B(C6 F5 )3 , despite featuring a pendant (non-fluorinated) aryl group and two flanking N-donors.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app