Published May 14, 2019
| Supplemental Material
Journal Article
Open
Zirconium complexes supported by a ferrocene-based ligand as redox switches for hydroamination reactions
Abstract
The synthesis of (thiolfan*)Zr(Net_2)_2 (thiolfan* = 1,1′-bis(2,4-di-tert-butyl-6-thiophenoxy)ferrocene) and its catalytic activity for intramolecular hydroamination are reported. In situ oxidation and reduction of the metal complex results in reactivity towards different substrates. The reduced form of (thiolfan*)Zr(Net_2)_2 catalyzes hydroamination reactions of primary aminoalkenes, whereas the oxidized form catalyzes hydroamination reactions of secondary aminoalkenes.
Additional Information
© 2019 The Royal Society of Chemistry. The article was received on 06 Feb 2019, accepted on 08 Apr 2019 and first published on 08 Apr 2019. This work was supported by the National Science Foundation (Grant CHE-1809116 to P. L. D. and CHE-1048804 for NMR spectroscopy) and UCLA. Yi Shen is grateful for an INFEWS fellowship (NSF Grant DGE-1735325). There are no conflicts to declare.Attached Files
Supplemental Material - c9cc01076a1_si.pdf
Files
c9cc01076a1_si.pdf
Files
(3.4 MB)
Name | Size | Download all |
---|---|---|
md5:dfdd956a242772e915eb6247a3059f4a
|
3.4 MB | Preview Download |
Additional details
- Eprint ID
- 95068
- DOI
- 10.1039/c9cc01076a
- Resolver ID
- CaltechAUTHORS:20190429-091330429
- CHE-1809116
- NSF
- CHE-1048804
- NSF
- University of California Los Angeles (UCLA)
- DGE-1735325
- NSF Graduate Research Fellowship
- Created
-
2019-04-29Created from EPrint's datestamp field
- Updated
-
2021-11-16Created from EPrint's last_modified field