Periodic polymers based on a self-accelerating click reaction

2018 ◽  
Vol 9 (29) ◽  
pp. 4036-4043 ◽  
Author(s):  
Lue Xiang ◽  
Zi Li ◽  
Jian'an Liu ◽  
Jiqiang Chen ◽  
Minghui Zhang ◽  
...  

Self-accelerating click chemistry was used to prepare sequence-controlled periodic polymers with ultrahigh molecular weights or a cyclic molecular topology.

2014 ◽  
Vol 5 (13) ◽  
pp. 4002-4008 ◽  
Author(s):  
Hong Du ◽  
Guangyu Zha ◽  
Lilong Gao ◽  
Huan Wang ◽  
Xiaodong Li ◽  
...  

Novel biodegradable antimicrobial hydrogels, which are promising for use as biomaterials, were prepared facilely via a thiol–ene “click” reaction under human physiological conditions using multifunctional poly(ethylene glycol) (PEG) derivatives as precursors.


Synthesis ◽  
2019 ◽  
Vol 52 (05) ◽  
pp. 673-687 ◽  
Author(s):  
Yan-Ping Meng ◽  
Shi-Meng Wang ◽  
Wan-Yin Fang ◽  
Zhi-Zhong Xie ◽  
Jing Leng ◽  
...  

The sulfur(VI) fluoride exchange reaction (SuFEx), developed by Sharpless and co-workers in 2014, is a new category of click reaction that creates molecular connections with absolute reliability and unprecedented efficiency through a sulfur(VI) hub. Ethenesulfonyl fluoride (ESF), as one of the most important sulfur(VI) hubs, exhibits extraordinary reactivity in SuFEx click chemistry and organic synthesis. This review summarizes the chemical properties and applications of ESF in click chemistry, organic chemistry, materials science, medicinal chemistry and in many other fields related to organic synthesis.1 Introduction2 Chemical Transformations of ESF3 Chemical Transformations of 2-Arylethenesulfonyl Fluorides4 Novel SuFEx Reagents Derived from ESF5 Applications of ESF Derivatives in Medicinal Chemistry6 Applications of ESF Derivatives in Materials Science7 Conclusion


2012 ◽  
Vol 584 ◽  
pp. 8-12 ◽  
Author(s):  
Balakrishna Kolli ◽  
Sarada P. Mishra ◽  
Mukesh P. Joshi ◽  
S. Raj Mohan ◽  
T.S. Dhami ◽  
...  

Click chemistry is used for synthesizing polymers for second order NLO study. The molecular weights found by gel-permeation chromatography (GPC), were in the range of 7000-55000 g/mol. Differential scanning calorimetry shows glass transition temperature (Tg) above 120 oC. From electronic spectra order parameter of the poled films were calculated to be 0.1-0.5. The change in surface morphology after poling was checked by atomic force microscopy. By using a pulsed Nd:YAG laser (1064nm), the second harmonic generation (SHG) intensity was measured. The SHG intensity was also studied as a function of against temperature and time respectively.


2017 ◽  
Vol 1 (1) ◽  
pp. 22-34
Author(s):  
Mariana Barbosa ◽  
Cristina Martins ◽  
Paula Gomes

In recent years, there has been a growing demand for novel strategies for biomedical applications. Chitosan is a typical cationic amino-containing polysaccharide that has been widely used due to its unique properties. The grafting modification of chitosan has been explored as an interesting method to develop multifunctional novel chitosan hybrid materials for drug delivery, tissue engineering, and other biomedical applications. Recently, “click” chemistry has been introduced into the synthesis of polymeric materials with well-defined and complex chain architectures. The Huisgen’s 1,3-dipolar cycloaddition reaction between alkynes and azides yielding triazoles is the principal example of a “click” reaction. Bioconjugation, surface modification, and orthogonal functionalization of polymers were successfully performed through this chemoselective reaction. In recent literature interest has been shown in this cycloaddition for the modification of polysaccharides, however, only a few chitosan graft copolymers have been synthesized by this technique.


2021 ◽  
Author(s):  
Dhruba Poudel ◽  
Richard Taylor

Protecting group free, one-pot multicomponent Curtius reaction was utilized to afford diurethane G-1 dendron. In our synthetic approach, G-1 dendron can undergo late-stage modification using thiol-ene click reaction, which was then attached to the core to furnish a dendrimer. In another approach, the G-1 dendron was attached to the core and so formed dendrimer was surface functionalized using thiol-ene click chemistry. Either way, we can synthesize the dendrimer.


2020 ◽  
Vol 8 (16) ◽  
pp. 4626-4637 ◽  
Author(s):  
Anne Nguyen ◽  
Hidenori Ando ◽  
Roland Böttger ◽  
K. K. DurgaRao Viswanadham ◽  
Elham Rouhollahi ◽  
...  

Click chemistry was used to study the effect of varied PEG molecular weights on the self-assembly of PEG-gambogic acid (GA) conjugates into nanoparticles.


2020 ◽  
Vol 6 (21) ◽  
pp. eaaz6107 ◽  
Author(s):  
R. Tian ◽  
S.-M. Xu ◽  
Q. Xu ◽  
C. Lu

To achieve efficient polymer-based room-temperature phosphorescence (RTP) materials, covalently embedding phosphors into the polymer matrix appeared as the most appealing approach. However, it is still highly challenging to fabricate RTP materials on a large scale because of the inefficient binding engineering and time-consuming covalent reactions. Here, we have proposed a scalable preparation approach for RTP materials by the facile B─O click reaction between boronic acid–modified phosphors and polyhydroxy polymer matrix. The ab initio molecular dynamics simulations demonstrated that the phosphors were effectively immobilized, resulting in the suppressed nonradiative transitions and activated RTP emission. In comparison to the reported covalent binding time of several hours, such a B─O click reaction can be accomplished within 20 s under ambient environment. The developed strategy simplified the construction of polymer-based RTP polymeric materials by the introduction of facile click chemistry. Our success provides inspirations and possibilities for the scale-up production of RTP materials.


2018 ◽  
Vol 42 (4) ◽  
pp. 3078-3086 ◽  
Author(s):  
Reza Bonyasi ◽  
Mohammad Gholinejad ◽  
Fariba Saadati ◽  
Carmen Nájera

Highly water dispersible CuFe2O4@Starch catalyzed click reaction.


Molecules ◽  
2020 ◽  
Vol 25 (18) ◽  
pp. 4339
Author(s):  
Chao-Da Xiao ◽  
Zhi-Yong He ◽  
Chuan-Xin Guo ◽  
Xiang-Chun Shen ◽  
Yan Xu

G-quadruplexes are non-canonical four stranded secondary structures possessing great biological importance. Controlling G-quadruplex conformation for further regulating biological processes is both exciting and challenging. In this study, we described a method for regulating G-quadruplex conformation by click chemistry for the first time. 8-ethynyl-2′-deoxyguanosine was synthesized and incorporated into a 12-nt telomere DNA sequence. Such a sequence, at first, formed mixed parallel/anti-parallel G-quadruplexes, while it changed to anti-parallel after reaction with azidobenzene. Meanwhile, the click reaction can give the sequence intense fluorescence.


2019 ◽  
Vol 55 (6) ◽  
pp. 731-750 ◽  
Author(s):  
Puja Saha ◽  
Deepanjan Panda ◽  
Jyotirmayee Dash

The Cu(i)-catalyzed azide and alkyne 1,3-dipolar cycloaddition (CuAAC), commonly known as the “click reaction”, has emerged as a versatile synthetic tool for targeting quadruplex nucleic acids.


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