2006
DOI: 10.1016/j.molcata.2005.08.048
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Application of molten salts in hydroalkoxycarbonylation of styrene

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Cited by 19 publications
(7 citation statements)
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“…The amount of palladium in this organic phase was found to be 209 ppm,indicating that 22 % of the initial amount of palladium was in the organic phase. This result is in agreement with the results reported in the literature[5][6][7][8] and can undoubtedly be attributed to the marked hydrophobic character of PPh 3 ligand. To solve this problem, the use of ionic ligands such as the sodium salts of sulfonated mono and bidentate arylphosphines have been considered.…”
supporting
confidence: 93%
“…The amount of palladium in this organic phase was found to be 209 ppm,indicating that 22 % of the initial amount of palladium was in the organic phase. This result is in agreement with the results reported in the literature[5][6][7][8] and can undoubtedly be attributed to the marked hydrophobic character of PPh 3 ligand. To solve this problem, the use of ionic ligands such as the sodium salts of sulfonated mono and bidentate arylphosphines have been considered.…”
supporting
confidence: 93%
“…Improved reaction rate and lower regioselectivity were observed with PdCl 2 /PPh 3 /CuCl 2 -NBu 4 Br system. The chloride-bromide exchange in the coordination sphere of palladium was shown by 31 P NMR [74].…”
Section: Homogeneous Catalytic Hydroalkoxycarbonylation In Ilsmentioning
confidence: 98%
“…Ammonium and phosphonium salts were also proved to be suitable media for the alkoxycarbonylation of styrene [13]. Using the PdCl 2 /PPh 3 /CuCl 2 system at 50 bar CO pressure and 110 C, almost complete conversion and acceptable regioselectivity, 74-78% towards the branched regioisomer, could be reached.…”
Section: Alkoxycarbonylationmentioning
confidence: 99%