Reductive electropolymerization of N-methyl-3-pyridylethynyl-porphyrins

2015 ◽  
Vol 51 (3) ◽  
pp. 519-521 ◽  
Author(s):  
Sung-Chou Huang ◽  
Ching-Yao Lin

The first reductive electropolymerization of porphyrins was studied by cyclic voltammetry, UV-visible and FT-IR spectroscopy, and theoretical calculations.

2011 ◽  
Vol 335-336 ◽  
pp. 989-993
Author(s):  
Mi Ouyang ◽  
Zhen Wei Yu ◽  
Yi Xu ◽  
Yu Jian Zhang ◽  
Cheng Zhang

Copolymers based on 1, 4-diethoxybenzene (DEB) and 3, 4-ethylenedioxythiophene (EDOT) were electrochemically synthesized and characterized. The structures of the copolymers were established by 1H NMR and FT-IR spectroscopy. The results indicated the final product was a copolymer instead of a blend or a composite. The physical properties were systematically investigated by cyclic voltammetry, UV-vis absorption and fluorescence. The PL maximum of copolymers presented obviously red-shift to long wavelength as the feed ratio of EDOT in monomer mixture increased.


2016 ◽  
Vol 18 (20) ◽  
pp. 5518-5528 ◽  
Author(s):  
Raihana Imran Khan ◽  
Kasi Pitchumani

An ionic Pd(ii) complex stabilized by a water soluble pyridinium modified β-cyclodextrin was prepared and characterized by NMR, mass spectrometry, FT-IR spectroscopy, UV-visible spectroscopy and DLS (dynamic light scattering).


2013 ◽  
Vol 634-638 ◽  
pp. 1981-1984
Author(s):  
Chun Yu Zhang ◽  
Hai Jun Niu ◽  
Lin Zhang ◽  
Xu Duo Bai

Polymerization of p-chloroaniline (CA) was achieved electrochemically in aqueous solution containing H2SO4 as supporting electrolyte. The films were obtained by applying sequential linear potential scan rate 20mV/s between -0.5 to 1.5V versus Ag/AgCl electrode. The polymer was characterized by UV-visible and FT-IR spectroscopy. We observed the morphologies of PCA films through the scanning electronic microscope (SEM), showing island protruding structure. The Tafel curves showed that PCA can be used as anti-corrosion material.


2020 ◽  
Vol 11 (1) ◽  
pp. 101-105
Author(s):  
Ashis K Sarker

In this work, we report carbon-silicon bond formation in thiophene, assisted with alkylated silylchloride. The formylation reaction of silylated thiophene has been discussed and achieved 61% overall yield of reactions. The compounds obtained are characterized quantitatively and qualitatively by using elemental analysis, FT-IR spectroscopy, UV/Visible spectroscopy, and proton NMR spectroscopy. This research work will boost chemists to make the carbon-silicon bond and utilize them in various applications. Journal of Engineering Science 11(1), 2020, 101-105


Author(s):  
Maciej Strzempek ◽  
Karolina A. Tarach ◽  
Kinga Góra-Marek ◽  
Fernando Rey ◽  
Miguel Palomino ◽  
...  

Abstract In this article the results of the statistical MC modelling corroborated by the FT-IR spectroscopy and gravimetric adsorption studies of the low aliphatic hydrocarbons in ZSM-5 (Si/Al =28 or...


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