Molecular Recognition and Enantiomer Separations on a novel chiral stationary phase based on a 9,9?-spirobi[9H-fluorene]-derived molecular cleft

1997 ◽  
Vol 80 (3) ◽  
pp. 897-911 ◽  
Author(s):  
Jens Cuntze ◽  
Fran�ois Diederich
Molecules ◽  
2021 ◽  
Vol 26 (2) ◽  
pp. 493
Author(s):  
Atsushi Ohnishi ◽  
Tohru Shibata ◽  
Tatsuya Imase ◽  
Satoshi Shinkura ◽  
Kanji Nagai

To understand the selectivity of the crown ether type chiral stationary phase (CSP), the retention selectivity for aniline and the positional isomers of substituted anilines were studied. In various substituted isomers, except nitroaniline, a remarkable decrease of retention due to steric hindrance was observed for the 2-substituted isomer. To determine the detailed molecular recognition mechanism, quantum chemical calculations were performed for the aggregates between the crown ether and the anilines. The results suggested that the 20-Crown-6, which includes a phenyl-substituted 1,1′-binaphthyl moiety, interacts with alkyl and aryl amines in an unconventional form different from the proposed one for 18-Crown-6.


Author(s):  
Chunye Liu ◽  
Yanqing Miao ◽  
Yihui Guo ◽  
Yinjuan An ◽  
Yunfang Li ◽  
...  

2016 ◽  
Vol 34 (1) ◽  
pp. 34 ◽  
Author(s):  
Rongji DAI ◽  
Huiting WANG ◽  
Weiwei SUN ◽  
Yulin DENG ◽  
Fang LV ◽  
...  

1990 ◽  
Vol 112 (11) ◽  
pp. 4573-4574 ◽  
Author(s):  
Per Erlandsson ◽  
Ingrid Marle ◽  
Lennart Hansson ◽  
Roland Isaksson ◽  
Goeran Pettersson ◽  
...  

2014 ◽  
Vol 53 (3) ◽  
pp. 431-435 ◽  
Author(s):  
T. Nemeth ◽  
S. Levai ◽  
T. F di ◽  
J. Kupai ◽  
G. Turos ◽  
...  

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