Borane-bridged ruthenium complex bearing a PNP Ligand: synthesis and structural characterization
Reaction of the precursor complex [RuHCl(CO)(PPh3)3] with the PNP protioligand CbzdiphosH in toluene resulted in the formation of two stereoisomeric hydrido complexes, [(CbzdiphosH)RuHCl(CO)] (A). The addition of a strong base (KOtBu or LiEt3BH), on the other hand, led to the formation of the 1,2-de...
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| Main Authors: | , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
October 2, 2015
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| In: |
Organometallics
Year: 2015, Volume: 34, Issue: 20, Pages: 5113-5118 |
| ISSN: | 1520-6041 |
| DOI: | 10.1021/acs.organomet.5b00699 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/acs.organomet.5b00699 |
| Author Notes: | Yijing Xu, Christoph A. Rettenmeier, Gudrun T. Plundrich, Hubert Wadepohl, Markus Enders and Lutz H. Gade |
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| 520 | |a Reaction of the precursor complex [RuHCl(CO)(PPh3)3] with the PNP protioligand CbzdiphosH in toluene resulted in the formation of two stereoisomeric hydrido complexes, [(CbzdiphosH)RuHCl(CO)] (A). The addition of a strong base (KOtBu or LiEt3BH), on the other hand, led to the formation of the 1,2-dehydrochlorination product [(Cbzdiphos)RuH(CO)]. The reaction of the latter with BH3·THF at room temperature led to the 1,2-addition of the BH3 moiety to the Ru-N function, forming a RuNBH cycle in [(CbzdiphosHBH2)RuH(CO)] (B). The same borane-bridged compound was obtained when complex A was treated with NaBH4 in THF. The BH2 group forms a bridging unit between the carbazole-N atom and one of the ruthenium-bound hydrides. | ||
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