scholarly journals Ionic liquids and supercritical carbon dioxide as solvents for NHPI-catalysed oxidation reactions

2019 ◽  
Author(s):  
Beata Orlińska ◽  
Gabriela Dobras ◽  
Dawid Lisicki
2016 ◽  
Vol 32 (6) ◽  
Author(s):  
Ruixia Liu ◽  
Peng Zhang ◽  
Suojiang Zhang ◽  
Ting Yan ◽  
Jiayu Xin ◽  
...  

AbstractIonic liquids (ILs) and supercritical CO


2009 ◽  
Vol 11 (4) ◽  
pp. 538 ◽  
Author(s):  
Pedro Lozano ◽  
Teresa De Diego ◽  
Corina Mira ◽  
Kimberley Montague ◽  
Michel Vaultier ◽  
...  

2010 ◽  
Vol 46 (36) ◽  
pp. 6705 ◽  
Author(s):  
Sanjib Kumar Karmee ◽  
Lasse Greiner ◽  
Alexander Kraynov ◽  
Thomas E. Müller ◽  
Bernd Niemeijer ◽  
...  

ChemSusChem ◽  
2011 ◽  
Vol 4 (8) ◽  
pp. 1035-1048 ◽  
Author(s):  
Luis Álvarez de Cienfuegos ◽  
Rafael Robles ◽  
Delia Miguel ◽  
José Justicia ◽  
Juan M. Cuerva

ChemInform ◽  
2011 ◽  
Vol 43 (1) ◽  
pp. no-no
Author(s):  
Luis Alvarez de Cienfuegos ◽  
Rafael Robles ◽  
Delia Miguel ◽  
Jose Justicia ◽  
Juan M. Cuerva

Author(s):  
Pedro Lozano ◽  
Teresa De Diego ◽  
Michel Vaultier ◽  
Jose L Iborra

Supercritical fluids and ionic liquids are neoteric solvents that can be used as non-conventional reaction media for enzymatic catalysis under optimised conditions. These solvents exhibit many different physical and chemical properties, but have two cross-points: they are not-miscible and can be easily separated from substrates and products, and they can be reused. As supercritical carbon dioxide (scCO2) can dissolve in the ionic liquid (IL) phase (up to 0.7 mole fraction), a new concept of biphasic bioreactors for Fine Chemicals syntheses may be developed by using both enzyme and chemical catalysts "immobilized" into the IL phase, and substrates transported by the scCO2 phase. The system was tested for the continuous chemoenzymatic dynamic kinetic resolution (DKR) of rac-1-phenylethanol in IL/scCO2 by using simultaneously immobilized lipase (Novozym 435) and acid zeolites catalysts at 50°C and 100 bars, providing good yields (up 98.0 %) for R-phenylethyl propionate ester with excellent enantioselectivity (up to 97.3 %), and without any activity loss after 14 days of operation.


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