scholarly journals A hyper-branched polymer tunes the size and enhances the fluorescent properties of aggregation-induced emission nanoparticles

2020 ◽  
Vol 2 (2) ◽  
pp. 633-641 ◽  
Author(s):  
Javad Tavakoli ◽  
Nikita Joseph ◽  
Colin L. Raston ◽  
Youhong Tang

The host–guest interaction approach, specifically via the formation of hydrogen bonds, is an effective strategy for preparing luminescent hyper-branched polymers.

2017 ◽  
Vol 25 (10) ◽  
pp. 602-606 ◽  
Author(s):  
S. A. Burikov ◽  
A. M. Vervald ◽  
K. A. Laptinskiy ◽  
T. V. Laptinskaya ◽  
O. A. Shenderova ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-8 ◽  
Author(s):  
Mathias S. Weyland ◽  
Harold Fellermann ◽  
Maik Hadorn ◽  
Daniel Sorek ◽  
Doron Lancet ◽  
...  

We propose an automaton, a theoretical framework that demonstrates how to improve the yield of the synthesis of branched chemical polymer reactions. This is achieved by separating substeps of the path of synthesis into compartments. We use chemical containers (chemtainers) to carry the substances through a sequence of fixed successive compartments. We describe the automaton in mathematical terms and show how it can be configured automatically in order to synthesize a given branched polymer target. The algorithm we present finds an optimal path of synthesis in linear time. We discuss how the automaton models compartmentalized structures found in cells, such as the endoplasmic reticulum and the Golgi apparatus, and we show how this compartmentalization can be exploited for the synthesis of branched polymers such as oligosaccharides. Lastly, we show examples of artificial branched polymers and discuss how the automaton can be configured to synthesize them with maximal yield.


Author(s):  
Ying Fu ◽  
Xiao-Xiao Pang ◽  
Kui Wang ◽  
Zhi-Qiang Wang ◽  
Guan-Yu Li ◽  
...  

A series of novel N-n-butyl-1,8-naphthalimide derivatives were synthesized via a three-step reaction involving nucleophilic substitution and acylation. All of the compounds were characterized by IR, 1H NMR, 13C NMR, MS, and elemental analysis, and the crystal structure of N-n-butyl-4-[N’,N’-bis(2`,4`-dichlorobenzoyl)ethylamino]-1,8-naphthalimide was determined. The π-π stacking interactions and hydrogen bonds between the two molecular core planes (naphthalimide ring) and the van der Waals forces between the flexible n-butyl groups resulted in a 3D long-chain structure. The UV-vis and fluorescence properties of the title compounds were investigated. The results indicated that the monosubstituted 1,8-naphthalimide derivatives bearing an electron-donating group on the benzene ring or a structure with a larger conjugative effect exhibited enhanced fluorescence properties.


2021 ◽  
Author(s):  
Jingfei Wang ◽  
Lifeng Xu ◽  
Shuangling Zhong ◽  
Yongyan Yang ◽  
Gangying Feng ◽  
...  

Numerous polymers without traditional chromophores show novel fluorescent properties and wide application prospect. This concept is referred to as non-traditional intrinsic luminescence (NTIL). Most polymers show aggregation-induced emission (AIE) characteristics....


2016 ◽  
Vol 45 (20) ◽  
pp. 8316-8319 ◽  
Author(s):  
Dan Wang ◽  
Shu-Mu Li ◽  
Yu-Fei Li ◽  
Xiang-Jun Zheng ◽  
Lin-Pei Jin

3-Aminopyridine-2-carboxylic acid can serve as an AIE-active turn on fluorescence chemosensor for Zn2+. The AIE behaviors are attributed to the cooperative effect of J-aggregation and hydrogen bonds. And selecting proper ratio of the solvents can prove the sensitivity.


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