Synthesis and Photorefractive Property of a Polymer Containing Azobenzene Group in the Side Chain

2002 ◽  
Vol 377 (1) ◽  
pp. 277-280 ◽  
Author(s):  
Phan-Seok Kim ◽  
Mi-Ra Kim ◽  
Gee-Young Sung ◽  
Ki-Hyun Kim ◽  
Chang-Sik Ha ◽  
...  
RSC Advances ◽  
2016 ◽  
Vol 6 (70) ◽  
pp. 65747-65755
Author(s):  
V. Novotná ◽  
A. Bobrovsky ◽  
V. Shibaev ◽  
D. Pociecha ◽  
M. Kašpar ◽  
...  

Novel LC monomer and corresponding polymethacrylate are synthesized and their phase behaviour, photooptical properties and photoorientation under polarized-light action are studied.


2008 ◽  
Vol 209 (20) ◽  
pp. 2071-2077 ◽  
Author(s):  
Shimon Tanaka ◽  
Hyun-Kyoung Kim ◽  
Astushi Sudo ◽  
Haruo Nishida ◽  
Takeshi Endo

Polymers ◽  
2020 ◽  
Vol 12 (4) ◽  
pp. 901 ◽  
Author(s):  
Jian Xu ◽  
Bin Niu ◽  
Song Guo ◽  
Xiaolei Zhao ◽  
Xiaoli Li ◽  
...  

The photoinduced solid-to-liquid transitions property of azobenzene-containing polymers (azopolymers) enables azopolymers with various promising applications. However, a general lack of knowledge regarding the influence of structure of the azobenzene derivatives on the photoinduced liquefaction hinders the design of novel azopolymers. In the present study, a series of azopolymers with side chains containing azobenzene unit bearing alkyl electron-donating groups were synthesized. The photoisomerization and photoinduced liquefaction properties of newly synthesized azopolymers were investigated. Alkyl-based electron-donating group significantly facilitate the photoisomerization process of azopolymers in solution, as the electron-donating ability of substituents increased, the time required for photoisomerization of azopolymers continually deceased. Meanwhile, the electron-donating group can drastically accelerate photoinduced solid-to-liquid transitions of azopolymers, the liquefaction rate of obtained azopolymers gradually getting quicker as the electron-donating ability of substituents increased. This study clearly demonstrates that the electron-donating group that bearing in the azobenzene group of polymer side chain play an essential role on the photoinduced solid-to-liquid transitions of azopolymers, and hence, gives an insight into how to design novel azopolymers for practical applications.


1998 ◽  
Vol 95 (6) ◽  
pp. 1351-1354 ◽  
Author(s):  
C.-M. Bouché ◽  
P. Le Barny ◽  
H. Facoetti ◽  
F. Soyer ◽  
P. Robin
Keyword(s):  

1984 ◽  
Vol 51 (03) ◽  
pp. 358-361 ◽  
Author(s):  
H Bechtold ◽  
K Andrassy ◽  
E Jähnchen ◽  
J Koderisch ◽  
H Koderisch ◽  
...  

SummaryIn 8 patients on no oral intake and with parenteral alimentation, administration of cephalosporins with N-methyl-thiotetrazole side chain (moxalactam, cefamandole), was associated with prolongation of prothrombin time, appearance in the circulation of descarboxy-prothrombin (counter immunoelectrophoresis and echis carinatus assay) and diminution of protein C. Acute administration of 10 mg vitamin Ki was followed by the transient appearance of vitamin K1 2,3-epoxide, indicating an impaired hepatocellular regeneration of vitamin K1 from the epoxide. Impaired hepatic vitamin K1 metabolism, tentatively ascribed to the N-methyl-thiotetrazole group, is one (but possibly not the only) cause of bleeding complications and depression of vitamin K1dependent procoagulants in patients treated with the new class of cephalosporins.


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