Coles, Nathan T. ![]() |
Official URL: https://doi.org/10.1021/acs.organomet.7b00326
Abstract
Dehydrocoupling of phosphine- and amine-boranes is reported using an iron(II) β-diketiminate complex. Dehydrocoupling of amine-boranes is far more facile than the phosphine counterpart, the former proceeding at room temperature with 1 mol% iron precatalyst. This low loading is sufficient to allow in situ kinetic analysis and deuterium labeling studies to be carried out. An iron amido-borane complex has also been isolated, which is believed to be the catalyst resting state. Overall, this has allowed us to postulate a catalytic cycle which proceeds via release of diborazane, iron hydride, and iron amido-borane intermediates.
Item Type: | Article |
---|---|
Status: | Published |
Schools: | Chemistry |
Publisher: | American Chemical Society |
ISSN: | 0276-7333 |
Last Modified: | 13 Nov 2024 11:30 |
URI: | https://orca.cardiff.ac.uk/id/eprint/173573 |
Actions (repository staff only)
![]() |
Edit Item |