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            <subfield code="a">10.2174/1876214X01003010044</subfield>
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            <subfield code="2">sideral</subfield>
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            <subfield code="a">eng</subfield>
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            <subfield code="a">Pardey, A.J.</subfield>
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        <datafield tag="245" ind1=" " ind2=" ">
            <subfield code="a">Hydroformylation of synthetic naphtha catalyzed by a dinuclear gem-dithiolato-bridged rhodium(I) complex</subfield>
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        <datafield tag="260" ind1=" " ind2=" ">
            <subfield code="c">2010</subfield>
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            <subfield code="a">This work focuses on the use of a gem-dithiolato-bridged rhodium(I) Rh 2(µ-S 2CBn 2)(cod) 2 complex (cod = 1,5-cyclooctadiene, Bn 2CS 2 2- = 1,3-diphenyl-2,2-dithiolatopropane) dissolved in toluene in the presence of monodentate phosphite P-donor ligand (P(OPh) 3) under carbon monoxide/hydrogen (1:1, syngas) atmosphere as an effective catalyst for hydroformylation of some olefins (oxo-reactions). The capability of this system to catalyze the hydroformylation of hex-1-ene, cyclohexene, 2,3-dimethyl-but-1-ene and 2-methyl-pent-2-ene and their quaternary mixture (synthetic naphtha) has been demonstrated. This innovative method to perform the in situ hydroformylation of the olefins present in naphthas to oxygenated products would be a promissory work for a future industrial catalytic process applicable to gasoline improving based on oxo-reactions. An important observation is that variation of CO/H 2 pressure (6.8-34.0 atm), temperature (60-80 oC), reaction time (2-10 h), rhodium concentration ((1.0-1.8)x10 -3 mol/L) affect hydroformylation reaction rates. Optimal conversion to oxygenated products were achieved under Rh = 1.8 x10 -2 mol/L, P(CO/H 2) = 34 atm (CO/H 2 = 1:1) at 80 oC for 10 h.</subfield>
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            <subfield code="a">Suárez, J.D.</subfield>
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            <subfield code="a">Ortega, M.C.</subfield>
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            <subfield code="a">Longo, C.</subfield>
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            <subfield code="0">(orcid)0000-0002-3327-0918</subfield>
            <subfield code="a">Pérez-Torrente, J.J.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="0">(orcid)0000-0001-7154-7239</subfield>
            <subfield code="a">Oro, L.A.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="1">2010</subfield>
            <subfield code="2">760</subfield>
            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Química Inorgánica</subfield>
            <subfield code="c">Área Química Inorgánica</subfield>
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        <datafield tag="773" ind1=" " ind2=" ">
            <subfield code="g">3, 1 (2010), 44-49</subfield>
            <subfield code="p">Open catal. j.</subfield>
            <subfield code="t">Open catalysis journal</subfield>
            <subfield code="x">1876-214X</subfield>
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