Synthesis, Structural Characterization, and Hydroformylation Activity of Rhodium(I) Complexes with a Polar Phosphinoferrocene Sulfonate Ligand
1′-(Diphenylphosphino)ferrocene-1-sulfonic acid (HL), isolated from the salt (Et3NH)L on an ion exchanger, reacts with Rh(I) complexes [Rh(acac)(CO)(PR3)] (acac = acetylacetonato-κ2 O,O′) to give complexes of the type [Rh(CO)(PR3)(Ph2PfcSO3-κ2 O,P)] (1a–d; R = Ph (a), Cy (b), 2-furyl (c), an...
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Published in | Organometallics Vol. 38; no. 2; pp. 479 - 488 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
American Chemical Society
28.01.2019
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Online Access | Get full text |
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Summary: | 1′-(Diphenylphosphino)ferrocene-1-sulfonic acid (HL), isolated from the salt (Et3NH)L on an ion exchanger, reacts with Rh(I) complexes [Rh(acac)(CO)(PR3)] (acac = acetylacetonato-κ2 O,O′) to give complexes of the type [Rh(CO)(PR3)(Ph2PfcSO3-κ2 O,P)] (1a–d; R = Ph (a), Cy (b), 2-furyl (c), and OMe (d); fc = ferrocene-1,1′-diyl). In an analogous reaction with [Rh(acac)(nbd)] (nbd = η2:η2-norbornadiene), HL produces [Rh(nbd)(Ph2PfcSO3-κ2 O,P)] (2). Adding (Et3NH)L (2 equiv per Rh) to [Rh(μ-Cl)(CO)2]2 and [Rh(acac)(CO)2] gives rise to the cationic complexes trans-(Et3NH)2[RhCl(CO)(Ph2PfcSO3-κP)2] (3) and (Et3NH)[Rh(CO)(Ph2PfcSO3-κ2O,P)(Ph2PfcSO3-κP)] (4), respectively. In complex 4, resulting from the simultaneous substitution of a CO ligand and acid–base replacement of the acac ligand, the P-monodentate and O,P-chelating phosphinoferrocene sulfonate ligands rapidly interconvert (in a solution). All compounds were characterized by spectroscopic methods and by elemental analysis, and the crystal structures of 1a·Me2CO, solvated 1b, 2, and 4·H2O were determined. Furthermore, the catalytic activity of all Rh(I) complexes was assessed in hydroformylation of vinyl acetate under solvent-free conditions at 80 °C and at 20 bar of synthesis gas (H2/CO = 1:1). High conversion with good selectivity to iso-aldehyde was observed for 1a·1/2H2O and 4·1/2H2O. When applied to “on-water” hydroformylation of 1-hexene (80 °C/10 bar), the complexes mainly promoted 1-hexene isomerization to 2-hexene. However, two of them, 1a·1/2H2O and 1c, exhibited reasonable selectivity to aldehydes and preferentially produced the linear product (n/iso ratios up to 3). |
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ISSN: | 0276-7333 1520-6041 |
DOI: | 10.1021/acs.organomet.8b00800 |