TY - JOUR
T1 - Water-soluble metal complexes and catalysts Part 6. A new, efficient water-soluble catalyst for two-phase hydroformylation of olefins
AU - Herrmann, Wolfgang A.
AU - Kohlpaintner, Christian W.
AU - Bahrmann, Helmut
AU - Konkol, Werner
PY - 1992/5
Y1 - 1992/5
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=0000010926&partnerID=8YFLogxK
U2 - 10.1016/0304-5102(92)80072-O
DO - 10.1016/0304-5102(92)80072-O
M3 - Article
AN - SCOPUS:0000010926
SN - 0304-5102
VL - 73
SP - 191
EP - 201
JO - Journal of Molecular Catalysis
JF - Journal of Molecular Catalysis
IS - 2
ER -