Issue 45, 2020

Bis(pentafluorophenyl)phenothiazylborane – an intramolecular frustrated Lewis pair catalyst for stannane dehydrocoupling

Abstract

We synthesized a novel Lewis acidic aminoborane containing a phenothiazyl substituent and demonstrated its potential to catalytically promote the dehydrocoupling of tin hydrides. The observed reactivity would imply a homolytic frustrated Lewis pair type mechanism, however computational analysis suggests a heterolytic mechanism for this reaction. This result represents one of the first frustrated Lewis pair systems to dehydrocouple stannanes in a heterolytic fashion.

Graphical abstract: Bis(pentafluorophenyl)phenothiazylborane – an intramolecular frustrated Lewis pair catalyst for stannane dehydrocoupling

Supplementary files

Article information

Article type
Communication
Submitted
11 Feb 2020
Accepted
27 Feb 2020
First published
05 Mär 2020

Dalton Trans., 2020,49, 16054-16058

Bis(pentafluorophenyl)phenothiazylborane – an intramolecular frustrated Lewis pair catalyst for stannane dehydrocoupling

J. N. Bentley, E. Pradhan, T. Zeng and C. B. Caputo, Dalton Trans., 2020, 49, 16054 DOI: 10.1039/D0DT00506A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements