Supramolecular polymer/metal salt complexes containing quadruple hydrogen bonding units

2007 ◽  
Vol 45 (23) ◽  
pp. 3181-3188 ◽  
Author(s):  
Kyung Ju Lee ◽  
Yong Woo Kim ◽  
Joo Hwan Koh ◽  
Jong Hak Kim
2007 ◽  
Vol 43 (10) ◽  
pp. 4460-4465 ◽  
Author(s):  
Kyung Ju Lee ◽  
Do Kyoung Lee ◽  
Yong Woo Kim ◽  
Jong Hak Kim

2021 ◽  
Vol 290 ◽  
pp. 01037
Author(s):  
Guangpu Zhang ◽  
Zhe Sun ◽  
Miaomiao Li

The microcrack of materials was inevitable in the process of transportation, storage and utilization, which may cause functional failure and resources waste. Inspired by nature, self-healing polymers have attracted significant attention owing to widespread applications in wearable electronics, cartilage replacement, coatings and elastomer. Compared with extrinsic healing, intrinsically healable polymers offer multiple self-healing by supramolecular reversible interactions, such as host-guest interactions, π-π stacking, ionic interactions and hydrogen-bonding. Self-healing polymers based on quadruple hydrogen bonds have been extensively investigated due to its high thermodynamic stability and rapid kinetic reversibility, and have been well developed for the past two decades. In this paper, the strategies and designs of self-repairing polymers based on quadruple hydrogen bond were classified and summarized, including main-chain self-healing polymers, side-chain self-healing polymers and supramolecular self-healing polymers. It is expected that quadruple hydrogen bonding can be construct more robust, highly tough, multi-stimuli-responsive, and fast self-healing supramolecular polymer, and is potential to be applied to numerous civilian and military fields in the future.


RSC Advances ◽  
2019 ◽  
Vol 9 (16) ◽  
pp. 8905-8911 ◽  
Author(s):  
Lei Kan ◽  
Peng Zhang ◽  
Hongkun Jiang ◽  
Shuai Zhang ◽  
Zhengdao Liu ◽  
...  

The supramolecular polymers based on 2-ureido-4[1H]-pyrimidone (UPy) with different structure were prepared and the effects of microtopography on the viscoelasticity were investigated.


2020 ◽  
Vol 1 (5) ◽  
pp. 1330-1336
Author(s):  
Jie Liu ◽  
Yubing Zhang ◽  
Chonghua Zhang ◽  
Peisheng Zhang ◽  
Rongjin Zeng ◽  
...  

The quadruple hydrogen bonding UPy units are designed to conjugate with unsubstituted PDI to exhibit bright red emission in aggregated state, together with temperature-dependent ratiometric fluorescence property in solution and hydrogels.


2018 ◽  
Vol 9 (44) ◽  
pp. 5395-5401 ◽  
Author(s):  
Shaobo Tan ◽  
Ye Sha ◽  
Tianyu Zhu ◽  
Md Anisur Rahman ◽  
Chuanbing Tang

A photoresponsive quadruple hydrogen-bonded supramolecular polymer was constructed using photochromic azobenzene and ureidopyrimidinone motifs.


Molecules ◽  
2021 ◽  
Vol 26 (15) ◽  
pp. 4705
Author(s):  
Boer Liu ◽  
Xi Chen ◽  
Glenn A. Spiering ◽  
Robert B. Moore ◽  
Timothy E. Long

This work reveals the influence of pendant hydrogen bonding strength and distribution on self-assembly and the resulting thermomechanical properties of A-AB-A triblock copolymers. Reversible addition-fragmentation chain transfer polymerization afforded a library of A-AB-A acrylic triblock copolymers, wherein the A unit contained cytosine acrylate (CyA) or post-functionalized ureido cytosine acrylate (UCyA) and the B unit consisted of n-butyl acrylate (nBA). Differential scanning calorimetry revealed two glass transition temperatures, suggesting microphase-separation in the A-AB-A triblock copolymers. Thermomechanical and morphological analysis revealed the effects of hydrogen bonding distribution and strength on the self-assembly and microphase-separated morphology. Dynamic mechanical analysis showed multiple tan delta (δ) transitions that correlated to chain relaxation and hydrogen bonding dissociation, further confirming the microphase-separated structure. In addition, UCyA triblock copolymers possessed an extended modulus plateau versus temperature compared to the CyA analogs due to the stronger association of quadruple hydrogen bonding. CyA triblock copolymers exhibited a cylindrical microphase-separated morphology according to small-angle X-ray scattering. In contrast, UCyA triblock copolymers lacked long-range ordering due to hydrogen bonding induced phase mixing. The incorporation of UCyA into the soft central block resulted in improved tensile strength, extensibility, and toughness compared to the AB random copolymer and A-B-A triblock copolymer comparisons. This study provides insight into the structure-property relationships of A-AB-A supramolecular triblock copolymers that result from tunable association strengths.


Author(s):  
Yufang Song ◽  
Yiming Chen ◽  
Ran Chen ◽  
Hongji Zhang ◽  
Dongjian Shi ◽  
...  

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