Transparent and mechanically strong hydrogen-bonded polymer complex elastomers with improved self-healability under ambient conditions

Polymer ◽  
2021 ◽  
Vol 218 ◽  
pp. 123461
Author(s):  
Yongjing Hu ◽  
Zhishuang Deng ◽  
Zhiwei Fan ◽  
Zhukang Du ◽  
Yinshu Su ◽  
...  
Author(s):  
Kiran Rehan ◽  
Chao Su ◽  
Jing Nie ◽  
Jian Xu ◽  
Shuguang Yang

2016 ◽  
Vol 5 (7) ◽  
pp. 814-818 ◽  
Author(s):  
Jiefu Li ◽  
Zhiliang Wang ◽  
Lingang Wen ◽  
Jing Nie ◽  
Shuguang Yang ◽  
...  

2019 ◽  
Vol 1 (1) ◽  
pp. 71-81 ◽  
Author(s):  
Jiefu Li ◽  
Jiaxing Sun ◽  
Di Wu ◽  
Wentao Huang ◽  
Meifang Zhu ◽  
...  

2006 ◽  
Vol 62 (7) ◽  
pp. o2669-o2671 ◽  
Author(s):  
Tatiana N. Drebushchak ◽  
Mikhail A. Mikhailenko ◽  
Elena V. Boldyreva ◽  
Tatyana P. Shakhtshneider

The title tetragonal polymorph is one of the two sulfathiazole–pyridine adducts, C9H9N3O2S2·C5H5N, that can be formed either by crystallization from an n-propanol–pyridine solution, or by exposure of solid sulfathiazole to pyridine vapour. The asymmetric unit consists of a hydrogen-bonded sulfathiazole–pyridine pair. Hydrogen bonds of the form Naniline—H...Osulfonyl form a three-dimensional network. Pyridine molecules linked to sulfathiazole molecules by Namino—H...Npyridine hydrogen bonds are located in the channels of the sulfathiazole framework which extend along the 41 axis. The angle between neighbouring pyridine rings in the channels is 55.2 (3)°. The adduct is stable in pyridine vapour, but decomposes in air under ambient conditions, giving the metastable polymorph I of sulfathiazole [Kruger & Gafner (1972). Acta Cryst. B28, 272–283].


2018 ◽  
Vol 36 (9) ◽  
pp. 1036-1042 ◽  
Author(s):  
Chao Su ◽  
Song-Mei Ma ◽  
Geng-Xin Liu ◽  
Shu-Guang Yang

RSC Advances ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 3606-3614 ◽  
Author(s):  
Yadong Zhang ◽  
Ke Zhang ◽  
Lei Wu ◽  
Ke Liu ◽  
Rui Huang ◽  
...  

Viologen-based porous ionic polymers with halogen anions and hydrogen-bonded water were constructed for efficient catalytic CO2 fixation under mild conditions.


2018 ◽  
Vol 54 (91) ◽  
pp. 12875-12878 ◽  
Author(s):  
Santhosh K. Matam ◽  
Russell F. Howe ◽  
Adam Thetford ◽  
C. Richard A. Catlow

At high loading, methanol reacts under ambient conditions with acidic hydroxyls of H-ZSM-5 to methoxylate framework oxygen; while a significant proportion remains hydrogen bonded to the framework with protonated geometry.


Author(s):  
Miaomiao Zhu ◽  
Weijie Wang ◽  
Caihong Zhang ◽  
Liping Zhu ◽  
Shuguang Yang

Author(s):  
Yan Liu ◽  
Chongwei An ◽  
Jin Luo ◽  
Jingyu Wang

The main challenge for achieving better energetic materials is to increase their density. In this paper, cocrystals of HNIW (2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane, often referred to as CL-20) with TNT (2,4,6-trinitrotoluene) were synthesized using ethanol in a green chemical method. The cocrystal was formulated as C13H11N15O18 and possesses a higher density (1.934 g cm−3) than published previously (1.846 g cm−3). This high-density cocrystal possesses a new structure, which can be substantiated by the different types of hydrogen bonds. The predominant driving forces that connect HNIW with TNT in the new cocrystal were studied at ambient conditions using single-crystal X-ray diffraction, powder X-ray diffraction, Fourier transform–infrared spectroscopy and Raman spectroscopy. The results reveal that the structure of the new HNIW/TNT cocrystals consists of three one-dimensional hydrogen-bonded chains exploiting the familiar HNIW–TNT multi-component supramolecular structure, in which two hydrogen-bonded chains are between —NO2 (HNIW) and —CH (TNT), and one hydrogen-bonded chain is between —CH (HNIW) and —NO2 (TNT). The changes to the electron binding energy and type of element in the new cocrystal were traced using X-ray photoelectron spectroscopy. Meanwhile, the physicochemical characteristics alter after cocrystallization due to the hydrogen bonding. It was found that the new HNIW/TNT cocrystal is more thermodynamically stable than HNIW. Thermodynamic aspects of new cocrystal decomposition are investigated in order to explain this observation. The detonation velocity of new HNIW/TNT cocrystals is 8631 m s−1, close to that of HNIW, whereas the mechanical sensitivity is lower than HNIW.


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