Ion-pair aggregation of a long-chain carboxylic acid and an amine in benzene studied by induced circular dichroism

Author(s):  
Shunsuke Takenaka ◽  
Mikiko Sugiyama ◽  
Niichiro Tokura
RSC Advances ◽  
2013 ◽  
Vol 3 (26) ◽  
pp. 10242 ◽  
Author(s):  
Eduardo Troche-Pesqueira ◽  
Ignacio Pérez-Juste ◽  
Armando Navarro-Vázquez ◽  
María Magdalena Cid

1980 ◽  
Vol 70 (1) ◽  
pp. 22-26 ◽  
Author(s):  
Akio Tajiri ◽  
Hidemi Hirayama ◽  
Masahiro Hatano

2013 ◽  
Vol 69 (11) ◽  
pp. 1411-1413 ◽  
Author(s):  
Yuko Kawanami ◽  
Hidekazu Tanaka ◽  
Jun-ichi Mizoguchi ◽  
Nobuko Kanehisa ◽  
Gaku Fukuhara ◽  
...  

The absolute configuration has been established of the enantiopureanti-head-to-head cyclodimer of anthracene-2-carboxylic acid (AC) cocrystallized with L-propinol and dichloromethane [systematic name: (S)-2-(hydroxymethyl)pyrrolidin-1-ium (5R,6S,11R,12S)-8-carboxy-5,6,11,12-tetrahydro-5,12:6,11-bis([1,2]benzeno)dibenzo[a,e][8]annulene-2-carboxylate dichloromethane monosolvate], C5H12NO+·C30H19O4−·CH2Cl2. In the crystal structure, the AC dimer interacts with L-prolinol through a nine-membered hydrogen-bonded ring [R22(9)], while the dichloromethane molecule is incorporated to fill the void space. The absolute configuration determined in this study verifies a recent assignment made by comparing theoreticalversusexperimental circular dichroism spectra.


2017 ◽  
Vol 50 (17) ◽  
pp. 6433-6438 ◽  
Author(s):  
Young-Jae Jin ◽  
Kyo-Un Seo ◽  
Young-Ghil Choi ◽  
Masahiro Teraguchi ◽  
Toshiki Aoki ◽  
...  

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