Novel columnar liquid crystalline oligomers: Triphenylene tetramers with rigid aromatic Schiff-bases and hydrogen-bonding spacers via click chemistry

2017 ◽  
Vol 236 ◽  
pp. 76-80 ◽  
Author(s):  
Shengjie Jiang ◽  
Hongyu Guo ◽  
Shuyun Zhu ◽  
Fafu Yang
1992 ◽  
Vol 12 (3) ◽  
pp. 403-415 ◽  
Author(s):  
V. A. Burmistrov ◽  
V. V. Alexandriysky ◽  
O. I. Koifman

2021 ◽  
Vol 3 (3) ◽  
pp. 1602-1609
Author(s):  
Flavia Lupi ◽  
Daniele Martella ◽  
Sara Nocentini ◽  
Diego Antonioli ◽  
Michele Laus ◽  
...  

2011 ◽  
Vol 356-360 ◽  
pp. 48-51
Author(s):  
Qi Tong ◽  
Ti Feng Jiao

In order to investigate the intermolecular hydrogen bonding of special amphiphiles, two bolaform amphiphilic Schiff bases (GN1 and GN2) with different hydrophilic spacers were designed, and their interaction with barbituric acid were tested by liquid chromatography. The chromatographic properties showed that both the Schiff bases showed hydrogen bonding interaction with barbituric acid. In addition, the influence of various detectors was also studied on both cases. Experimental results show that the test with FLD showed better determination than other detectors. It is proposed that due to the directionality and strong matching of hydrogen bond, one barbituric acid molecule can be encapsulated into the intramolecular area of GN1, while two barbituric acid molecules were trapped into the GN2 molecule through intermolecular H-bonds for GN2 due to the long spacer and flexible structure. A rational complex mode was proposed.


2014 ◽  
Vol 753 ◽  
pp. 42-47 ◽  
Author(s):  
Gyandshwar Kumar Rao ◽  
Arun Kumar ◽  
Mahabir Pratap Singh ◽  
Ajay Kumar ◽  
Ashok Manikrao Biradar ◽  
...  

2017 ◽  
Vol 41 (14) ◽  
pp. 6514-6522 ◽  
Author(s):  
Yuki Arakawa ◽  
Yukito Sasaki ◽  
Kazunobu Igawa ◽  
Hideto Tsuji

A novel class of hydrogen bonding liquid crystalline benzoic acids with alkylthio groups was established and their phase transition behavior was investigated in detail.


Author(s):  
Koshiro Maegawa ◽  
Hiroki Tanimoto ◽  
Seiji Onishi ◽  
Takenori Tomohiro ◽  
Tsumoru Morimoto ◽  
...  

Organic azides are still in the center of click chemistry connecting two molecules. However, taming the conjugation selectivity of azides is difficult without the help of the bulky groups. We...


2011 ◽  
Vol 52 (2) ◽  
pp. 227-233 ◽  
Author(s):  
G. A. Zhurko ◽  
V. V. Aleksandriiskii ◽  
V. A. Burmistrov

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