scholarly journals Novel Conjugated Polymer Containing Aromatic Ring and Selenium in Backbone. Kinetics of the Addition Reaction as the Model for Addition Polymerization

1995 ◽  
Vol 27 (2) ◽  
pp. 156-164 ◽  
Author(s):  
Nobuki Metaka ◽  
Eiichi Kobayashi ◽  
Sadahito Aoshima ◽  
Junji Furukawa
2020 ◽  
Vol 39 (2) ◽  
pp. 227
Author(s):  
Adnan Kurt ◽  
Hacer Andan ◽  
Murat Koca

A new conjugated polymer containing a bithiazole group is prepared by the polycondensation of 2,2'-diamino-4,4'-bithiazole and terephthaldialdehyde in the presence of glacial acetic acid. The kinetics of thermal degradation of the new polymer are investigated by thermogravimetric analysis at different heating rates. The temperature corresponding to the maximum rate loss shifts to higher temperatures with increasing heating rate. The thermal decomposition activation energies of the conjugated polymer in a conversion range of 3–15 % are 288.4 and 281.1 kJ/mol by the Flynn–Wall–Ozawa and Kissinger methods, respectively. The Horowitz–Metzger method shows that the thermodegradation mechanism of the conjugated polymer proceeds over a three-dimensional diffusion type deceleration D3 mechanism. The optimum heating rate is 20 ºC/min.


2019 ◽  
Vol 2019 ◽  
pp. 1-8
Author(s):  
Masanori Hirose ◽  
Shigenori Sugisaki ◽  
Keishi Suga ◽  
Hiroshi Umakoshi

A method to detect the L-proline- (L-Pro-) catalyzed Michael addition reaction in model biomembranes has been established, using N-[p(2-benzimidazolyl)phenyl]maleimide and acetone as reactants. The effect of liposome membranes on this reaction was kinetically analyzed using fluorescence spectroscopy. The kinetics of the reaction were different from those of the constituent lipids of the liposomes. Zwitterionic 1,2-dipalmitoyl-sn-glycero-3-phosphocholine liposome, which is in the solid-ordered phase, had a better value of reaction rate, suggesting that the reaction rate constants of this reaction in liposome membrane systems could be regulated by the characteristics of the liposome membrane (i.e., the phase state and surface charge). Based on the results obtained, a plausible model of the L-Pro-catalyzed Michael addition reaction was discussed. The obtained results provide us with an easily detectable method to assess the reactivity of L-Pro in biological systems.


RSC Advances ◽  
2016 ◽  
Vol 6 (86) ◽  
pp. 83466-83470 ◽  
Author(s):  
Daihui Zhang ◽  
Marie-Josée Dumont ◽  
Alice Cherestes

A derivative of 5-hydroxymethylfurfural was synthesized for the thiol-Michael addition reaction.


1990 ◽  
Vol 22 (12) ◽  
pp. 1035-1042 ◽  
Author(s):  
Eiichi Kobayashi ◽  
Takatsugu Obata ◽  
Sadahito Aoshima ◽  
Junji Furukawa

2012 ◽  
Vol 14 (39) ◽  
pp. 13532 ◽  
Author(s):  
Tomoyasu Hirai ◽  
Kaoru Kawasaki ◽  
Keiji Tanaka

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