Direct Observation of Transmetalation from a Neutral Boronate Ester to a Pyridine(diimine) Iron Alkoxide
Transmetallation of the neutral boronate esters, (2-benzofuranyl)BPin and (2-benzofuranyl)BNeo (Pin = pinacolato, Neo = neopentylglycolato) to a representative pyridine(diimine) iron alkoxide complex, (iPrPDI)FeOEt (iPrPDI = 2,6-(2,6-iPr2-C6H3N=CMe)2C5H3N; R = Me, Et, SiMe3), to yield the correspond...
| Veröffentlicht in: | Organometallics. - 1998. - 39(2020), 1 vom: 13. Jan., Seite 201-205 |
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| 1. Verfasser: | |
| Weitere Verfasser: | , , , , |
| Format: | Online-Aufsatz |
| Sprache: | English |
| Veröffentlicht: |
2020
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| Zugriff auf das übergeordnete Werk: | Organometallics |
| Schlagworte: | Journal Article |
| Zusammenfassung: | Transmetallation of the neutral boronate esters, (2-benzofuranyl)BPin and (2-benzofuranyl)BNeo (Pin = pinacolato, Neo = neopentylglycolato) to a representative pyridine(diimine) iron alkoxide complex, (iPrPDI)FeOEt (iPrPDI = 2,6-(2,6-iPr2-C6H3N=CMe)2C5H3N; R = Me, Et, SiMe3), to yield the corresponding iron benzofuranyl derivative was studied. Synthesis of the requisite iron alkoxide complexes was accomplished either by salt metathesis between (iPrPDI)FeCl and NaOR (R = Me, Et, SiMe3) or by protonation of the iron alkyl, (iPrPDI)FeCH2SiMe3, by the free alcohol R'OH (R' = Me, Et). A combination of magnetic measurements, X-ray diffraction, NMR and Mössbauer spectroscopies and DFT calculations identified each (iPrPDI)FeOR compound as an essentially planar, high-spin, S = 3/2 compound engaged in antiferromagnetic coupling with a radical anion on the chelate (S Total = 3/2; S Fe = 2, S PDI = 1/2). The resulting iron benzofuranyl product, (iPrPDI)Fe(2-benzofuranyl) was characterized by X-ray diffraction and in combination with magnetic measurements, spectroscopic and computational data, was identified as an overall S = 1/2 compound, demonstrating that a net spin-state change accompanies transmetallation (S Fe = 1, S PDI = 1/2). These findings may be relevant to further development of iron-catalyzed Suzuki-Miyaura cross-coupling with neutral boronate esters and alkoxide bases |
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| Beschreibung: | Date Revised 13.01.2021 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
| ISSN: | 0276-7333 |
| DOI: | 10.1021/acs.organomet.9b00733 |