Binary Supramolecular Gels Based on Bismelamine·Cyanurate/Barbiturate Noncovalent Polymers

2004 ◽  
Vol 16 (19) ◽  
pp. 3582-3585 ◽  
Author(s):  
Shiki Yagai ◽  
Masatsugu Higashi ◽  
Takashi Karatsu ◽  
Akihide Kitamura

Author(s):  
Laurent Latxague ◽  
Sébastien Benizri ◽  
Alexandra Gaubert ◽  
James Tolchard ◽  
Denis Martinez ◽  
...  


2021 ◽  
Author(s):  
Santanu Panja ◽  
Dave J. Adams

Stimuli responsive dynamic changes in the networks of self-assembled gels result in an alteration of physical and chemical properties of the gel with time.



2021 ◽  
Vol 205 ◽  
pp. 109759
Author(s):  
Liangchun Li ◽  
Rongqin Sun ◽  
Renlin Zheng ◽  
Yi Huang
Keyword(s):  


RSC Advances ◽  
2021 ◽  
Vol 11 (21) ◽  
pp. 12641-12648
Author(s):  
Renyuan Chen ◽  
Caidie Xu ◽  
Yihao Lei ◽  
Hongxin Liu ◽  
Yabin Zhu ◽  
...  

A family of low molecular weight gelators with different alkyl chain lengths was constructed, having excellent gelation ability and antibiotic loading capacity. A low molecular weight hydrogelator was obtained by adjusting the length of alkyl chain.





2021 ◽  
Vol 03 (02) ◽  
pp. 174-183
Author(s):  
P. Chidchob ◽  
S. A. H. Jansen ◽  
S. C. J. Meskers ◽  
E. Weyandt ◽  
N. P. van Leest ◽  
...  

The introduction of a chemical additive to supramolecular polymers holds high potential in the development of new structures and functions. In this regard, various donor- and acceptor-based molecules have been applied in the design of these noncovalent polymers. However, the incorporation of boron–nitrogen frustrated Lewis pairs in such architectures is still rare despite their many intriguing properties in catalysis and materials science. The limited choices of suitable boron derivatives represent one of the main limitations for the advancement in this direction. Here, we examine the use of the commercially available tris(pentafluorophenyl)borane with various triphenylamine derivatives to create supramolecular B–N charge transfer systems. Our results highlight the importance of a proper balance between the donor/acceptor strength and the driving force for supramolecular polymerization to achieve stable, long-range ordered B–N systems. Detailed analyses using electron paramagnetic resonance and optical spectroscopy suggest that tris(pentafluorophenyl)borane displays complex behavior with the amide-based triphenylamine supramolecular polymers and may interact in dimers or larger chiral aggregates, depending on the specific structure of the triphenylamines.



2019 ◽  
Vol 33 (5) ◽  
pp. e4845 ◽  
Author(s):  
Ruru Xue ◽  
Saisai Wei ◽  
Xuelin Dong ◽  
Tingyu Zhu ◽  
Jianhui Yuan ◽  
...  


2010 ◽  
Vol 49 (38) ◽  
pp. 6718-6724 ◽  
Author(s):  
Jonathan A. Foster ◽  
Jonathan W. Steed
Keyword(s):  


ChemInform ◽  
2009 ◽  
Vol 40 (12) ◽  
Author(s):  
Hiromitsu Maeda
Keyword(s):  


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