Abstract
Reaction of a magnesium diboranate complex with triphenylphosphine oxide provides a terminal magnesium boryl, which is itself a potent reagent for the deoxygenative reduction of Ph 3PO. Computational analysis with density functional theory (DFT) indicates that B-B bond activation results from initial coordination of the P=O bond of the phosphine oxide to magnesium.
| Original language | English |
|---|---|
| Pages (from-to) | 9035 - 9038 |
| Number of pages | 4 |
| Journal | Chemical communications (Cambridge, England) |
| Volume | 55 |
| Issue number | 61 |
| Early online date | 4 Jul 2019 |
| DOIs | |
| Publication status | Published - 7 Aug 2019 |
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- General Chemistry
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry
Fingerprint
Dive into the research topics of 'Diborane heterolysis and P(v) reduction by Ph 3P=O coordination to magnesium'. Together they form a unique fingerprint.Projects
- 2 Finished
-
Nucleophilic alkaline earth boryls: from conception and theory to application
Hill, M. (PI), Cresswell, A. (CoI) & McMullin, C. (Researcher)
Engineering and Physical Sciences Research Council
1/05/18 → 31/07/22
Project: Research council
-
Augmentation of Alkaline Earth Reactivity: An FLP Analogy
Hill, M. (PI)
Engineering and Physical Sciences Research Council
8/02/16 → 6/02/20
Project: Research council
Equipment
-
Balena High Performance Computing (HPC) System
Facility/equipment: Equipment
-
High Performance Computing (HPC) Facility
Chapman, S. (Manager)
University of BathFacility/equipment: Facility
Cite this
- APA
- Standard
- Harvard
- Vancouver
- Author
- BIBTEX
- RIS