Inverted Piano Stools: A Molecular Recognition Motif That Enforces 1:1 Cocrystallization of Two Diastereomers in the Same Single Crystal

2003 ◽  
Vol 42 (16) ◽  
pp. 1859-1862 ◽  
Author(s):  
Henri Brunner ◽  
Matthias Weber ◽  
Manfred Zabel ◽  
Thomas Zwack
RSC Advances ◽  
2014 ◽  
Vol 4 (36) ◽  
pp. 18763-18771 ◽  
Author(s):  
Guocan Yu ◽  
Jie Yang ◽  
Danyu Xia ◽  
Yong Yao

A novel molecular recognition motif between a water-soluble pillar[5]arene (WP5) and acetylcholine is established with an association constant of (5.05 ± 0.13) × 104 M−1.


2004 ◽  
Vol 16 (11) ◽  
pp. 3033-3044 ◽  
Author(s):  
Rajnish Khanna ◽  
Enamul Huq ◽  
Elise A. Kikis ◽  
Bassem Al-Sady ◽  
Christina Lanzatella ◽  
...  

2016 ◽  
Vol 7 (22) ◽  
pp. 3669-3673 ◽  
Author(s):  
Lili Wang ◽  
Zhe Sun ◽  
Miaomiao Ye ◽  
Yu Shao ◽  
Lei Fang ◽  
...  

A photo-responsive cross-linked supramolecular polymer was prepared based on a ternary host–guest molecular recognition motif between cucurbit[8]uril and 1,1-dimethyl-4,4-bipyridinium dication and azobenzene derivative, and its AIE behavior was also investigated.


2015 ◽  
Vol 56 (16) ◽  
pp. 2091-2093 ◽  
Author(s):  
Yujuan Zhou ◽  
Kecheng Jie ◽  
Connor Thompson ◽  
Ning Li ◽  
Yong Yao

2017 ◽  
Vol 41 (3) ◽  
pp. 916-919 ◽  
Author(s):  
Yujuan Zhou ◽  
Kecheng Jie ◽  
Yong Yao

A novel pH-responsive molecular recognition motif was built between an anionic carboxylate group modified resorcin[4]arene and paraquat in water. We then employed it to fabricate a supra-amphiphile for controllable self-assembly.


2015 ◽  
Vol 6 (2) ◽  
pp. 218-222 ◽  
Author(s):  
Kecheng Jie ◽  
Yujuan Zhou ◽  
Xiaofan Ji

Based on the bis(m-phenylene)-32-crown-10/paraquat molecular recognition motif in water, we have successfully prepared an amphiphilic supramolecular graft copolymer by the combination of modified hydrophilic poly(ethylene oxide) and hydrophobic polystyrene. It could self-assemble into pH-responsive bilayer vesicles in water.


2017 ◽  
Vol 4 (12) ◽  
pp. 2387-2391 ◽  
Author(s):  
Yujuan Zhou ◽  
Kecheng Jie ◽  
Feihe Huang

A novel redox-responsive molecular recognition motif was built between a neutral selenium-containing pillar[5]arene and a pyridinium bromide salt in water. It was further used to construct the first pillararene-based selenium-containing supramolecular amphiphile with application in controlled release.


2010 ◽  
Vol 82 (12) ◽  
pp. 2281-2294 ◽  
Author(s):  
Jason M. Spruell

This article highlights the emerging use of the interactions of radical π-dimers to drive both molecular recognition and switching processes within supramolecular systems and mechanically interlocked molecular architectures. The enhanced stability experienced by dimers of radical cation species when encapsulated, as compared to when they are free in solution, is driving their useful incorporation into functional systems. The redox stimulation used in the production of radical cation species provides the ideal trigger for molecular switching events. Moreover, the nature and strength of the radical dimerization events introduces a completely novel recognition motif within supramolecular and mechanically interlocked molecular systems, complementing well-established techniques and enabling new research opportunities to blossom.


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