Abstract
A series of sulfonated biphenylphosphanes were readily prepared from commercially available, inexpensive, and air-stable organic compounds. Of these, the trisulfonated trisbiphenylphosphane can be considered as a true water-soluble analogue of PPh3 as the cone angle and basicity of both phosphanes are very close and result in a similar coordination mode on palladium and rhodium complexes. The catalytic performance of the trisulfonated trisbiphenylphosphane was evaluated in the aqueous hydroformylation of 1-decene and the Tsuji-Trost reaction. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Ferreira, M., Bricout, H., Hapiot, F., Sayede, A., Tilloy, S., & Monflier, E. (2008). A property-matched water-soluble analogue of the benchmark ligand PPh 3. ChemSusChem, 1(7), 631–636. https://doi.org/10.1002/cssc.200800097
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