Preparation of Fluorine‐Free Waterproof and Breathable Electrospun Nanofibrous Membranes via thiol‐ene Click Reaction

2022 ◽  
pp. 2100757
Author(s):  
Lulu Tian ◽  
Gaihuan Ren ◽  
Pan Zhang ◽  
Bo Li ◽  
Shuzhen Chang ◽  
...  
Keyword(s):  
Click Reaction ◽  
Nanofibrous Membranes

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

Highly efficient photodegradation of various organic pollutants in water: Rational structural design of photocatalyst via thiol-ene click reaction

2020 ◽  
Vol 381 ◽  
pp. 122631 ◽  
Author(s):  
Fei Liu ◽  
Yibing Sun ◽  
Jiayu Gu ◽  
Qianhong Gao ◽  
Dongping Sun ◽  
...  
Keyword(s):  
Organic Pollutants ◽  
Structural Design ◽  
Click Reaction ◽  
Highly Efficient

Electrospun nanofibrous membranes of cellulose acetate containing hydroxyapatite co-doped with Ag/Fe: morphological features, antibacterial and degradation of methylene blue from aqueous solutions

2021 ◽  
Author(s):  
Ahmed Esmail Shalan ◽  
M. Afifi ◽  
M.M. El-Desoky ◽  
M.k Ahmed
Keyword(s):  
Methylene Blue ◽  
Aqueous Solutions ◽  
Cellulose Acetate ◽  
Morphological Features ◽  
Molar Ratio ◽  
Electrospinning Technique ◽  
Nanofiber Membranes ◽  
Nanofibrous Membranes ◽  
Co Doped

Cellulose acetate nanofiber membranes containing hydroxyapatite co-doped with Ag/Fe were efficaciously attained through the electrospinning technique. Different molar ratio compositions of hydroxyapatite co-doped with Ag/Fe in the structure of the...

Synthesis of copper containing polyaniline composites through interfacial polymerisation: An effective catalyst for Click reaction at room temperature

2021 ◽  
Vol 1233 ◽  
pp. 130019
Author(s):  
Mitali Chetia ◽  
Manashjyoti Konwar ◽  
Biswajit Pegu ◽  
Surajit Konwer ◽  
Diganta Sarma
Keyword(s):  
Room Temperature ◽  
Click Reaction ◽  
Effective Catalyst ◽  
Polyaniline Composites

scholarly journals Electrospun Nanostructured Membrane Engineering Using Reverse Osmosis Recycled Modules: Membrane Distillation Application

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1601
Author(s):  
Jorge Contreras-Martínez ◽  
Carmen García-Payo ◽  
Mohamed Khayet
Keyword(s):  
Reverse Osmosis ◽  
Polyvinylidene Fluoride ◽  
Membrane Distillation ◽  
Permeate Flux ◽  
Electrospinning Technique ◽  
Salt Rejection ◽  
Rejection Factor ◽  
Nanofibrous Membranes ◽  
Membrane Engineering ◽  
Desalination Plants

As a consequence of the increase in reverse osmosis (RO) desalination plants, the number of discarded RO modules for 2020 was estimated to be 14.8 million annually. Currently, these discarded modules are disposed of in nearby landfills generating high volumes of waste. In order to extend their useful life, in this research study, we propose recycling and reusing the internal components of the discarded RO modules, membranes and spacers, in membrane engineering for membrane distillation (MD) technology. After passive cleaning with a sodium hypochlorite aqueous solution, these recycled components were reused as support for polyvinylidene fluoride nanofibrous membranes prepared by electrospinning technique. The prepared membranes were characterized by different techniques and, finally, tested in desalination of high saline solutions (brines) by direct contact membrane distillation (DCMD). The effect of the electrospinning time, which is the same as the thickness of the nanofibrous layer, was studied in order to optimize the permeate flux together with the salt rejection factor and to obtain robust membranes with stable DCMD desalination performance. When the recycled RO membrane or the permeate spacer were used as supports with 60 min electrospinning time, good permeate fluxes were achieved, 43.2 and 18.1 kg m−2 h−1, respectively; with very high salt rejection factors, greater than 99.99%. These results are reasonably competitive compared to other supported and unsupported MD nanofibrous membranes. In contrast, when using the feed spacer as support, inhomogeneous structures were observed on the electrospun nanofibrous layer due to the special characteristics of this spacer resulting in low salt rejection factors and mechanical properties of the electrospun nanofibrous membrane.

scholarly journals Photo Click Reaction of Acylsilanes with Indoles

2021 ◽  
Author(s):  
Constantin Stuckhardt ◽  
Maren Wissing ◽  
Armido Studer
Keyword(s):  
Click Reaction

scholarly journals Enhancing Toughness and Reducing Volumetric Shrinkage for Bis-GMA/TEGDMA Resin Systems by Using Hyperbranched Thiol Oligomer HMDI-6SH

Materials ◽  
2021 ◽  
Vol 14 (11) ◽  
pp. 2817
Author(s):  
Biao Yu ◽  
Jingwei He ◽  
Sufyan Garoushi ◽  
Pekka K. Vallittu ◽  
Lippo Lassila
Keyword(s):  
Water Sorption ◽  
Water Solubility ◽  
Click Reaction ◽  
Raw Materials ◽  
Triethylene Glycol ◽  
Bending Test ◽  
Volumetric Shrinkage ◽  
Dental Resin ◽  
System A ◽  
Double Bond Conversion

In order to improve the toughness and reduce polymerization shrinkage of traditional bisphenol A-glycidyl methacrylate (Bis-GMA)/triethylene glycol dimethacrylate (TEGDMA) based dental resin system, a hyperbranched thiol oligomer (HMDI-6SH) was synthesized via thiol-isocyanate click reaction using pentaerythritol tetra(3-mercaptopropionate (PETA) and dicyclohexylmethane 4,4′-diisocyanate (HMDI) as raw materials. Then HMDI-6SH was mixed with 1,3,5-Triallyl-1,3,5-Triazine-2,4,6(1H,3H,5H)-Trione (TTT) to prepare thiol-ene monomer systems, which were added into Bis-GMA/TEGDMA resins with different mass ratio from 10 wt% to 40 wt% to serve as anti-shrinking and toughening agent. The physicochemical properties of these thiol-ene-methacrylate ternary resins including functional groups conversion, volumetric shrinkage, flexural properties, water sorption, and water solubility were evaluated. The results showed that the incorporation of HMDI/TTT monomer systems into Bis-GMA/TEGDMA based resin could improve C=C double bond conversion from 62.1% to 82.8% and reduced volumetric shrinkage from 8.53% to 4.92%. When the mass fraction of HMDI/TTT monomer systems in the resins was no more than 20 wt%, the flexural strength of the resin was higher or comparable to Bis-GMA/TEGDMA based resins (p > 0.05). The toughness (it was measured from the stress–strain curves of three-point bending test) of the resins was improved. Water sorption and water solubility tests showed that the hydrophobicity of resin was enhanced with increasing the content of thioester moiety in resin.

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