New low-temperature NMR studies establish the presence of a second equatorial: apical isomer of [(R,S)-Binaphos](CO)2RhH
The important enantioselective hydroformylation catalyst [(R,S)-Binaphos](CO)2RhH has been reexamained by low-temperature NMR spectroscopy. Both 1H and 31P NMR spectroscopy at −90 °C allow direct observation of a mixture of two apical−equatorial chelates. The major chelate, 1eq,ap, was shown to have...
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| Hauptverfasser: | , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
6 July 2010
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| In: |
Organometallics
Year: 2010, Jahrgang: 29, Heft: 15, Pages: 3362-3367 |
| ISSN: | 1520-6041 |
| DOI: | 10.1021/om100323q |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/om100323q |
| Verfasserangaben: | Dante A. Castillo Molina, Charles P. Casey, Imke Müller, Kyoko Nozaki, and Christoph Jäkel |
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| 246 | 3 | 3 | |a New low-temperature NMR studies establish the presence of a second equatorial$dapical isomer of [(R,S)-Binaphos](CO) 2 RhH |
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| 520 | |a The important enantioselective hydroformylation catalyst [(R,S)-Binaphos](CO)2RhH has been reexamained by low-temperature NMR spectroscopy. Both 1H and 31P NMR spectroscopy at −90 °C allow direct observation of a mixture of two apical−equatorial chelates. The major chelate, 1eq,ap, was shown to have an equatorial phosphine and an apical phosphite. Its structure was unambiguously assigned using low-temperature 31P NMR spectroscopy with selective decoupling of aromatic hydrogens but not of the rhodium hydride, which showed a 225 Hz trans phosphite to RhH coupling. The equilibrium constant for [1eq,ap]/[1ap,eq] was determined over a wide temperature range. | ||
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