Journal
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 54, Issue 2, Pages 472-475Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201407707
Keywords
homogeneous catalysis; hydrotris(pyrazolyl)borate; PH bonds; P ligands; rhodium
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Funding
- MICINN/FEDER [CTQ2011-22516]
- Gobierno de Aragon/FSE (GA/FSE, Inorganic Molecular Architecture Group) [E70]
- NWO-CW (VICI) [016.122.613]
- NWO-CW (BdB)
- Gobierno de Aragon
- MEC
- Austrian Science Fund (FWF) [E70] Funding Source: Austrian Science Fund (FWF)
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Complexes with terminal phosphanido (MPR2) functionalities are believed to be crucial intermediates in new catalytic processes involving the formation of PP and PC bonds. We showcase here the isolation and characterization of mononuclear phosphanide rhodium complexes ([RhTp(H)(PR2)L]) that result from the oxidative addition of secondary phosphanes, a reaction that was also explored computationally. These compounds are active catalysts for the dehydrocoupling of PHPh2 to Ph2PPPh2. The hydrophosphination of dimethyl maleate and the unactivated olefin ethylene is also reported. Reliable evidence for the prominent role of mononuclear phosphanido rhodium species in these reactions is also provided.
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