2007
DOI: 10.1007/s11144-007-5023-6
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Hydroformylation of naphthas with a rhodium complex in biphasic medium

Abstract: The chlorocarbonyl bis-[butylphenyl (meta-sulfonate-phenyl)phosphine] rhodium (I) complex shows catalytic hydroformylation activity in toluene/water biphasic medium for 1-hexene, cyclohexene, 2,3-dimethyl-2-butene and 2-methyl-2-pentene, their binary mixtures and a real Venezuelan naphtha, under standardized reaction conditions (1000 psi of syngas (1:1 H 2 /CO), 100ºC, substrate/catalyst molar ratio (600:1) and 4 h reaction time), obtaining high percent conversion to oxygenated products.

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Cited by 8 publications
(7 citation statements)
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“…At present, our research is directed toward the synthesis of the sodium salt of sulfonated pyridine [12,13] as a water-soluble ligand with different metallic centers. The principal goal in this work is the application of rhodium biphasic systems to obtain fuels with high oxygenated products proportion, which would contribute to the improvement of the quality and performance of gasoline through a simple and unique process and finding a friendly environment alternative to avoid the use of ethanol as fuel additive [14][15][16][17][18][19].…”
Section: Introductionmentioning
confidence: 99%
“…At present, our research is directed toward the synthesis of the sodium salt of sulfonated pyridine [12,13] as a water-soluble ligand with different metallic centers. The principal goal in this work is the application of rhodium biphasic systems to obtain fuels with high oxygenated products proportion, which would contribute to the improvement of the quality and performance of gasoline through a simple and unique process and finding a friendly environment alternative to avoid the use of ethanol as fuel additive [14][15][16][17][18][19].…”
Section: Introductionmentioning
confidence: 99%
“…The catalytic carbonylation of olefins in naphtha by oxo or Reppe type process [1][2][3][4][5] has been studied as an alternative route to conventional catalytic alkylation and hydrogenation processes [6][7][8]. Olefins are desirable for their octane value but are unwanted because they lead to deposits and gum formation and increased emissions of ozone forming hydrocarbons and toxic compounds [9].…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, there is a need to explore other oxygenated additives more environmentally benign. An alternative to this approach can be the in situ transformation of the olefins present in naphtha into oxygenated compounds with high added value, likes esters, aldehydes and acetals, among others, via catalytic carbonylation which it can be carried out in one step avoiding the expensive catalytic hydrogenation [1][2][3][4][5].…”
Section: Introductionmentioning
confidence: 99%
“…The products coming from the catalytic carbonylation reactions of C6-C8 olefins by soluble and immobilized transition metal complexes offer access to wide range of important oxygenated compounds which could be used in a though be future industrial catalytic process for gasoline improving based on in situ carbonylation reaction over olefins present in naphtha [11].…”
Section: Introductionmentioning
confidence: 99%