NMR-spectroscopic studies on solvent electrophilic properties, Part II: Binary aqueous-non aqueous solvent systems

1977 ◽  
Vol 108 (2) ◽  
pp. 489-498 ◽  
Author(s):  
Ulrich Mayer ◽  
Wolfgang Gerger ◽  
Viktor Gutmann
2011 ◽  
Vol 72 (3-4) ◽  
pp. 122-129 ◽  
Author(s):  
Maija-Liisa Mattinen ◽  
Pekka Maijala ◽  
Paula Nousiainen ◽  
Annika Smeds ◽  
Jussi Kontro ◽  
...  

1977 ◽  
Vol 22 (3) ◽  
pp. 475-483 ◽  
Author(s):  
C.A.G.O. Varma ◽  
F.L. Plantenga ◽  
C.A.M. van den Ende ◽  
P.H.M. van Zeyl ◽  
J.J. Tamminga ◽  
...  

2006 ◽  
Vol 78 (1) ◽  
pp. 125-134 ◽  
Author(s):  
Michael Brad Strader ◽  
David L. Tabb ◽  
W. Judson Hervey ◽  
Chongle Pan ◽  
Gregory B. Hurst

Author(s):  
Lulu Fu ◽  
Chenghua Lu ◽  
Shengqiang Tong ◽  
Min Xu ◽  
Lan Tang ◽  
...  

Abstract Five non-polar phloroglucinol derivatives, viz. pseudo-aspidin, α-kosin and agripinol A-C were isolated and purified from Agrimonia pilosa Ledeb by semi-preparative counter-current chromatography. The separation was performed by a two-step elution with non-aqueous solvent systems. In the first step, an elution mode of a two-phase solvent system consisting of n-hexane-acetonitrile-dichloromethane-methanol (6:6:0.5:0.5, v/v/v/v) was used. We obtained sample Ι containing three components (47.0 mg) and sample ΙΙ containing two components (24.8 mg) from crude extract (371.0 mg). In the second step, sample Ι was successfully separated by closed-loop recycling mode with a solvent system consisting of n-hexane-acetonitrile-dichloromethane (10:7:3, v/v/v), yielding 17.8 mg of pseudo-aspidin, 18.5 mg of α-kosin and 6.4 mg of agripinol A. The other two compounds—8.7 mg of agripinol B and 13.6 mg of agripinol C—were obtained from sample ΙΙ in the same manner. All the isolated compounds had a high purity exceeding 95%.


1993 ◽  
Vol 71 (11) ◽  
pp. 1834-1840 ◽  
Author(s):  
Mark L. O'Neill ◽  
Peeter Kruus ◽  
Robert C. Burk

Spectroscopic studies of the compound 2-nitroanisole in supercritical fluids CO2 and N2O show that π* values vary linearly with density. The solubility trends in these single component supercritical fluid solvents qualitatively followed the trends in solvent power predicted from π*. However, the relative solvent power predicted for CO2 and N2O based on π* resulted in an opposite order to what was determined experimentally through solubility measurements. The π* parameter may be of some use for solubility prediction if only a limited set of solute–solvent systems are considered. Measurements of π*, especially those in binary supercritical fluid solvents, suggest that π* could be a valuable tool for probing the solute-organized cybotactic region.


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