Well-Defined Aryl-FeII Complexes in Cross-Coupling and C-H Activation Processes
© 2021 American Chemical Society.
Veröffentlicht in: | Organometallics. - 1998. - 40(2021), 9 vom: 10. Mai, Seite 1195-1200 |
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1. Verfasser: | |
Weitere Verfasser: | , , , , |
Format: | Online-Aufsatz |
Sprache: | English |
Veröffentlicht: |
2021
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Zugriff auf das übergeordnete Werk: | Organometallics |
Schlagworte: | Journal Article |
Zusammenfassung: | © 2021 American Chemical Society. Herein we explore the intrinsic organometallic reactivity of iron embedded in a tetradentate N3C macrocyclic ligand scaffold that allows the stabilization of aryl-Fe species, which are key intermediates in Fe-catalyzed cross-coupling and C-H functionalization processes. This study covers C-H activation reactions using Me L H and FeCl2, biaryl C-C coupling product formation through reaction with Grignard reagents, and cross-coupling reactions using Me L Br or H L Br in combination with Fe0(CO)5. Synthesis under light irradiation and moderate heating (50 °C) affords the aryl-FeII complexes [FeII(Br)( Me L)(CO)] (1 Me ) and [FeII( H L)(CO)2]Br (1 H ). Exhaustive spectroscopic characterization of these rare low-spin diamagnetic species, including their crystal structures, allowed the investigation of their intrinsic reactivity |
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Beschreibung: | Date Revised 28.09.2022 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
ISSN: | 0276-7333 |
DOI: | 10.1021/acs.organomet.1c00100 |