scholarly journals Recoverable and recyclable water-soluble sulphonated salicylaldimine Rh(i) complexes for 1-octene hydroformylation in aqueous biphasic media

2015 ◽  
Vol 44 (3) ◽  
pp. 1240-1248 ◽  
Author(s):  
Leah C. Matsinha ◽  
Selwyn F. Mapolie ◽  
Gregory S. Smith

A series of water-soluble Rh(i) mononuclear complexes of general formula: [Rh(sulphsal-X-R)(COD)] [sulphsal = sulphonated salicylaldimine, COD = cyclooctadiene; where R = H, Cl, CH3 and X = H, tBu] have been synthesized.

2015 ◽  
Vol 490 ◽  
pp. 163-169 ◽  
Author(s):  
Pablo J. Baricelli ◽  
Mariandry Rodriguez ◽  
Luis G. Melean ◽  
Maria Modroño Alonso ◽  
Margarita Borusiak ◽  
...  

2017 ◽  
Vol 61 (2) ◽  
Author(s):  
María Modroño-Alonso ◽  
William Castro ◽  
Francisco Lopez-Linares ◽  
Merlín Rosales ◽  
Pablo Jose Baricelli

The water soluble cobalt complex HCo(CO)[P(<em>o</em>-C<sub>6</sub>H<sub>4</sub>SO-<sub>3</sub>Na)]<sub>3</sub> was used as catalyst precursor for the biphasic aqueous hydroformylation of 1-hexene. The complex was synthesized by reductive carbonylation of CoCl<sub>2</sub>.6H<sub>2</sub>O in the presence of <em>o</em>-TPPTS ([P(<em>o</em>-C<sub>6</sub>H<sub>4</sub>SO<sub>3</sub>Na)]<sub>3</sub>) under nitrogen atmosphere and characterized by FTIR, <sup>1</sup>H NMR and <sup>31</sup>P {1H} NMR, <sup>13</sup>C NMR, DEPT – 135, COSY, HSQC, MS (ESI). The catalytic activity of the complex in the biphasic hydroformylation reaction of 1-hexene was evaluated under moderate reaction conditions. The pressure and temperature were varied from 4137 – 7584 kPa (600-1100 psi) of syngas and from 353 – 383 K (80 – 110 °C), respectively. The 1-hexene concentration was varied from 0.021-0,11M and the catalyst from 4x10<sup>-4</sup> - 1.1x10<sup>-3</sup> M. The best conversion at 363 K and 7584 kPa and 7.5 h was 62% with selectivity towards aldehydes (heptanal and 2-methyl-hexanal) of 66% to with l/b ratio of 2.6. The recycling of the catalytic precursor after four successive times, did not show any loss on the activity, having selectivity towards aldehyde up to 60%.


2021 ◽  
Author(s):  
Marco Bortoluzzi ◽  
Jesus Castro ◽  
Andrea Di Vera ◽  
Alberto Palù ◽  
Valentina Ferraro

Tetrahedral Mn(II) bromo- and iodo-complexes with phosphoramidate and phosphonate ligands were synthesized and characterized. Mononuclear complexes with general formula [MnX2L2] were isolated by using the monodentate ligands O=P(OPh)2(NMe2) and O=P(OPh)2Ph....


2017 ◽  
Vol 32 (3) ◽  
pp. e4111 ◽  
Author(s):  
Thangavel Thirunavukkarasu ◽  
H. Puschmann ◽  
H.A. Sparkes ◽  
Karuppannan Natarajan ◽  
V.G. Gnanasoundari

ChemInform ◽  
2010 ◽  
Vol 33 (42) ◽  
pp. no-no
Author(s):  
Shoichi Shimizu ◽  
Takashi Suzuki ◽  
Seiji Shirakawa ◽  
Yasuyuki Sasaki ◽  
Choichiro Hirai

1997 ◽  
Vol 62 (2) ◽  
pp. 355-363 ◽  
Author(s):  
Jan Čermák ◽  
Magdalena Kvíčalová ◽  
Vratislav Blechta

New homoleptic nickel(0) and palladium(0) complexes with a water-soluble ligand, 1,3,5-triaza-7-phosphaadamantane, were prepared and characterized by 1H, 13C, and 31P NMR spectra. The complexes, together with the known analogous Ni(0) and Pd(0) complexes with tris(hydroxymethyl)phosphine, were found to be catalysts for buta-1,3-diene oligomerization or telomerization with water in an aqueous biphasic system without a cosolvent or a modifier. Tetrakis[tris(hydroxymethyl)phosphine]nickel (7) preferentially catalyzes oligomerization (both linear and cyclic) in the first example of a nickel-catalyzed buta-1,3-diene oligomerization in an aqueous biphasic system. Palladium complexes give telomers or linear oligomers in quantitative yields. In the case of the triazaphosphaadamantane complex 4, high selectivity to octadienyl ethers (87%) was observed. High values of metal leaching into the product phase in these reactions suggest an easy extraction of starting or intermediate metal complexes caused by the fact that both monomer and products are good ligands for the metal complexes in this particular case.


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