scholarly journals Inside Cover: Selective Solid-Liquid and Liquid-Liquid Extraction of Lithium Chloride Using Strapped Calix[4]pyrroles (Angew. Chem. Int. Ed. 37/2018)

2018 ◽  
Vol 57 (37) ◽  
pp. 11824-11824 ◽  
Author(s):  
Qing He ◽  
Neil J. Williams ◽  
Ju Hyun Oh ◽  
Vincent M. Lynch ◽  
Sung Kuk Kim ◽  
...  
2018 ◽  
Vol 130 (37) ◽  
pp. 11998-11998
Author(s):  
Qing He ◽  
Neil J. Williams ◽  
Ju Hyun Oh ◽  
Vincent M. Lynch ◽  
Sung Kuk Kim ◽  
...  

2018 ◽  
Vol 130 (37) ◽  
pp. 12100-12104 ◽  
Author(s):  
Qing He ◽  
Neil J. Williams ◽  
Ju Hyun Oh ◽  
Vincent M. Lynch ◽  
Sung Kuk Kim ◽  
...  

2018 ◽  
Vol 57 (37) ◽  
pp. 11924-11928 ◽  
Author(s):  
Qing He ◽  
Neil J. Williams ◽  
Ju Hyun Oh ◽  
Vincent M. Lynch ◽  
Sung Kuk Kim ◽  
...  

1969 ◽  
Vol 18 (3) ◽  
pp. 398-399 ◽  
Author(s):  
Taitiro FUJINAGA ◽  
Toru KUWAMOTO ◽  
Eiichiro NAKAYAMA ◽  
Masatada SATAKE

2021 ◽  
Vol 68 (4) ◽  
pp. 765-772
Author(s):  
Lee Suan Chua ◽  
Abirame Segaran ◽  
Hoi Jin Wong

Phytochemicals in the water extract of Eurycoma longofolia roots were identified using both solid-liquid and liquid-liquid extraction based fractionation techniques. A reversed phase C18 solid phase extraction (SPE) was used as solid-liquid extraction, whereas solvent partition was applied as liquid-liquid extraction. Total saponin was increased after fractionation. A few known quassinoids; eurycomanone, 13α(21)-epoxyeurycomanone, pasakbumin D, 13β,18-dihydroeurycomanol and 13β,21-dihydroxyeurycomanol were identified from the 40% and 60% methanol fractions of SPE. Solvent partition extract using ethyl acetate was found to have the highest saponin content compared to butanol and chloroform fractions. Subsequent acetone precipitation of the organic fractions recovered a formylated hexose trimer and other saccharide-containing compounds. Ethyl acetate effectively recovered saponins from E. longofolia water extract using liquid-liquid extraction followed by acetone precipitation.


2020 ◽  
Vol 21 (24) ◽  
pp. 9465
Author(s):  
Marta Zaleskaya ◽  
Łukasz Dobrzycki ◽  
Jan Romański

A tripodal, squaramide-based ion-pair receptor 1 was synthesized in a modular fashion, and 1H NMR and UV-vis studies revealed its ability to interact more efficiently with anions with the assistance of cations. The reference tripodal anion receptor 2, lacking a crown ether unit, was found to lose the enhancement in anion binding induced by presence of cations. Besides the ability to bind anions in enhanced manner by the “single armed” ion-pair receptor 3, the lack of multiple and prearranged binding sites resulted in its much lower affinity towards anions than in the case of tripodal receptors. Unlike with receptors 2 or 3, the high affinity of 1 towards salts opens up the possibility of extracting extremely hydrophilic sulfate anions from aqueous to organic phase. The disparity in receptor 1 binding modes towards monovalent anions and divalent sulfates assures its selectivity towards sulfates over other lipophilic salts upon liquid–liquid extraction (LLE) and enables the Hofmeister bias to be overcome. By changing the extraction conditions from LLE to SLE (solid–liquid extraction), a switch of selectivity from sulfates to acetates was achieved. X-ray measurements support the ability of anion binding by cooperation of the arms of receptor 1 together with simultaneous binding of cations.


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