Abstract
The diphosphane 2,2′-bis(diphenylphosphinomethyl)-1,1′-biphenyl (1, BISBI) was sulfonated by means of oleum containing 65% SO3. The sulfonation product, 2 (BISBIS), was purified by extraction-reextraction techniques. The sodium salts, 3, of BISBIS (2) are accessible as a mixture of several sulfonated derivatives. In the heterogeneous (biphasic) hydroformylation of propene, this sulfonated ligand 3 yields exceptionally high n/iso ratios of the resulting butyric aldehyde (rhodium catalysis). High activity and productivity at low phosphane/rhodium ratios are additional advantages of using 3. Hydroformylation of higher olefins, e.g., 1-hexene, is also within the scope of the new catalytic Rh(I)/BISBIS system.
| Original language | English |
|---|---|
| Pages (from-to) | 191-201 |
| Number of pages | 11 |
| Journal | Journal of Molecular Catalysis |
| Volume | 73 |
| Issue number | 2 |
| DOIs | |
| State | Published - May 1992 |
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