Quantitative Introduction of Perfluoroalkyl Groups to Poly(diphenylacetylene) Membranes via Three-step Membrane Reaction Including Click Reaction and Their Gas Permeability

2015 ◽  
Vol 44 (12) ◽  
pp. 1679-1681 ◽  
Author(s):  
Takashi Sato ◽  
Masahiro Teraguchi ◽  
Motohiro Kiuchi ◽  
Takashi Kaneko ◽  
Toshiki Aoki
Keyword(s):  
Click Reaction ◽  
Gas Permeability ◽  
Membrane Reaction

ANALYSIS OF GAS PERMEABILITY FOR LIQUID PHASE-SINTERED POROUS SiC COMPACT

2014 ◽  
Vol 17 (8) ◽  
pp. 705-713 ◽  
Author(s):  
Hikaru Maeda ◽  
Yoshihiro Hirata ◽  
Soichiro Sameshima ◽  
Taro Shimonosono
Keyword(s):  
Liquid Phase ◽  
Gas Permeability ◽  
Porous Sic

Dynamic Emergence of Nanostructure and Transport Properties in Perfluorinated Sulfonic Acid Ionomers

2020 ◽  
Author(s):  
Adlai Katzenberg ◽  
Debdyuti Mukherjee ◽  
Peter J. Dudenas ◽  
Yoshiyuki Okamoto ◽  
Ahmet Kusoglu ◽  
...  
Keyword(s):  
Rate Constant ◽  
Sulfonic Acid ◽  
Mass Fraction ◽  
Gas Permeability ◽  
Transport Processes ◽  
Segmental Mobility ◽  
The Matrix ◽  
Swelling Rate ◽  
Ion Conducting ◽  
Perfluorinated Sulfonic Acid

<p>Limitations in fuel cell electrode performance have motivated the development of ion-conducting binders (ionomers) with high gas permeability. Such ionomers have been achieved by copolymerization of perfluorinated sulfonic acid (PFSA) monomers with bulky and asymmetric monomers, leading to a glassy ionomer matrix with chemical and mechanical properties that differ substantially from common PFSA ionomers (e.g., Nafion™). In this study, we use perfluorodioxolane-based ionomers to provide fundamental insights into the role of the matrix chemical structure on the dynamics of structural and transport processes in ion-conducting polymers. Through <i>in-situ</i> water uptake measurements, we demonstrate that ionomer water sorption kinetics depend strongly on the properties and mass fraction of the matrix. As the PFSA mass fraction was increased from 0.26 to 0.57, the Fickian swelling rate constant decreased from 0.8 s<sup>-1</sup> to 0.2 s<sup>-1</sup>, while the relaxation rate constant increased from 3.1×10<sup>-3</sup> s<sup>-1</sup> to 4.0×10<sup>-3</sup>. The true swelling rate, in nm s<sup>-1</sup>, was determined by the chemical nature of the matrix; all dioxolane-containing materials exhibited swelling rates ~1.5 - 2 nm s<sup>-1</sup> compared to ~3 nm s<sup>-1</sup> for Nafion. Likewise, Nafion underwent relaxation at twice the rate of the fastest-relaxing dioxolane ionomer. Reduced swelling and relaxation kinetics are due to limited matrix segmental mobility of the dioxolane-containing ionomers. We demonstrate that changes in conductivity are strongly tied to the polymer relaxation, revealing the decoupled roles of initial swelling and relaxation on hydration, nanostructure, and ion transport in perfluorinated ionomers. </p>

Synthetic Routes for 1,4-disubstituted 1,2,3-triazoles: A Review

2019 ◽  
Vol 23 (8) ◽  
pp. 860-900 ◽  
Author(s):  
Chander P. Kaushik ◽  
Jyoti Sangwan ◽  
Raj Luxmi ◽  
Krishan Kumar ◽  
Ashima Pahwa
Keyword(s):  
Solid Phase ◽  
Click Reaction ◽  
Biological Activities ◽  
Triazole Ring ◽  
Copper Catalysts ◽  
Biologically Active ◽  
Pharmaceutical Chemistry ◽  
Biological Targets ◽  
Synthetic Routes ◽  
High Yields

N-Heterocyclic compounds like 1,2,3-triazoles serve as a key scaffolds among organic compounds having diverse applications in the field of drug discovery, bioconjugation, material science, liquid crystals, pharmaceutical chemistry and solid phase organic synthesis. Various drugs containing 1,2,3-triazole ring which are commonly available in market includes Rufinamide, Cefatrizine, Tazobactam etc., Stability to acidic/basic hydrolysis along with significant dipole moment support triazole moiety for appreciable participation in hydrogen bonding and dipole-dipole interactions with biological targets. Huisgen 1,3-dipolar azide-alkyne cycloaddition culminate into a mixture of 1,4 and 1,5- disubstituted 1,2,3-triazoles. In 2001, Sharpless and Meldal came across with a copper(I) catalyzed regioselective synthesis of 1,4-disubstituted 1,2,3-triazoles by cycloaddition between azides and terminal alkynes. This azide-alkyne cycloaddition has been labelled as a one of the important key click reaction. Click synthesis describes chemical reactions that are simple to perform, gives high selectivity, wide in scope, fast reaction rate and high yields. Click reactions are not single specific reaction, but serve as a pathway for construction of simple to complex molecules from a variety of starting materials. In the last few decades, 1,2,3-triazoles attracted attention of researchers all over the world because of their broad spectrum of biological activities. Keeping in view the biological importance of 1,2,3-triazole, in this review we focus on the various synthetic routes for the syntheisis of 1,4-disubstituted 1,2,3-triazoles. This review involves various synthetic protocols which involves copper and non-copper catalysts, different solvents as well as substrates. It will boost synthetic chemists to explore new pathway for the development of newer biologically active 1,2,3-triazoles.

Green and Facile Synthesis of 1,4-Disubstituted 1,2,3-Triazoles via a Click Reaction of α-Bromo Ketones, [bmim]N3 and Terminal Acetylenes

2013 ◽  
Vol 10 (10) ◽  
pp. 738-743 ◽  
Author(s):  
Azadeh Fazeli ◽  
Hossein Oskooie ◽  
Yahya Beheshtiha ◽  
Majid Heravi ◽  
Hassan Valizadeh
Keyword(s):  
Click Reaction ◽  
Facile Synthesis ◽  
Terminal Acetylenes
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