Abstract
Phosphinooxazoline (PHOX) ligands have been used to control the regio- and enantioselectivity in a wide variety of metal-catalyzed reactions. Despite their widespread use, PHOX ligands have never been studied in metal-aryne complexes. Herein we report the first example of a PHOX-Ni aryne complex. As demonstrated in other systems, the differentiated P versus N donors and different steric environments of the unsymmetric ligand are able to induce regiocontrol. A 81:19 mixture of o-methoxy substituted aryne complexes is observed. Single-crystal X-ray crystallographic analysis, UV/vis spectroscopy, and cyclic voltammetry are used to gain further insight into the molecular and electronic structure of these complexes. Lastly, a methylation/deuteration sequence shows retention of the PHOX ligand-induced regiocontrol in the difunctionalized products and that the regiospecificity of these difunctionalizations is due to the trans influence of the P donor.
Original language | English (US) |
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Pages (from-to) | 97-101 |
Number of pages | 5 |
Journal | ACS Organic and Inorganic Au |
Volume | 4 |
Issue number | 1 |
DOIs | |
State | Published - Feb 7 2024 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2023 The Authors. Published by American Chemical Society
Keywords
- Nickel
- PHOX ligands
- arynes
- methylation
- regioselectivity
PubMed: MeSH publication types
- Journal Article