Preferential intermolecular interactions lead to chiral recognition: enantioselective gel formation and collapse

2018 ◽  
Vol 54 (81) ◽  
pp. 11407-11410 ◽  
Author(s):  
Diksha Gambhir ◽  
Sunil Kumar ◽  
Gourab Dey ◽  
Venkata Krishnan ◽  
Rik Rani Koner

Enantioselective recognition of chiral amines through gel formation and collapse.

2019 ◽  
Author(s):  
Nancy Watfa ◽  
Weimin Xuan ◽  
Zoe Sinclair ◽  
Robert Pow ◽  
Yousef Abul-Haija ◽  
...  

Investigations of chiral host guest chemistry are important to explore recognition in confined environments. Here, by synthesizing water-soluble chiral porous nanocapsule based on the inorganic metal-oxo Keplerate-type cluster, {Mo<sub>132</sub>} with chiral lactate ligands with the composition [Mo<sub>132</sub>O<sub>372</sub>(H<sub>2</sub>O)<sub>72</sub>(<i>x-</i>Lactate)<sub>30</sub>]<sup>42-</sup> (<i>x</i> = D or L), it was possible to study the interaction with a chiral guest, L/D-carnitine and (<i>R</i>/<i>S</i>)-2-butanol in aqueous solution. The enantioselective recognition was studied by quantitative <sup>1</sup>H NMR and <sup>1</sup>H DOSY NMR which highlighted that the chiral recognition is regulated by two distinct sites. Differences in the association constants (K) of L- and D-carnitine, which, due to their charge, are generally restricted from entering the interior of the host, are observed, indicating that their recognition predominantly occurs at the surface pores of the structure. Conversely, a larger difference in association constants (K<i><sub>S</sub></i>/K<i><sub>R</sub></i> = 3) is observed for recognition within the capsule interior of (<i>R</i>)- and (<i>S</i>)-2-butanol.


1994 ◽  
Vol 43 (10) ◽  
pp. 769-778
Author(s):  
Hisanobu OGOSHI ◽  
Tadashi EMA ◽  
Tadashi MIZUTANI

2015 ◽  
Vol 51 (23) ◽  
pp. 4823-4826 ◽  
Author(s):  
Zhongyue Sun ◽  
Fan Zhang ◽  
Xiaoyan Zhang ◽  
Demei Tian ◽  
Lei Jiang ◽  
...  

A label-free nanochannel for enantioselective recognition of d-, l-Arg by adding BSA as chiral selector has been fabricated. Before adding BSA, the nanochannel cannot discriminate d- and l-Arg while with addition of BSA, this nanochannel displayed good enantioselectivity.


RSC Advances ◽  
2015 ◽  
Vol 5 (31) ◽  
pp. 24499-24506 ◽  
Author(s):  
Kumaresh Ghosh ◽  
Anupam Majumdar

A series ofl-amino acid derived pyridinium-based chiral compounds have been designed and synthesized. Among them, somel-valine derivatives show enantioselective recognition ofd-lactate in fluorescence.


CrystEngComm ◽  
2021 ◽  
Author(s):  
Yang Li ◽  
Shumei Chen ◽  
Zhong-Xuan Xu ◽  
Xin Wu ◽  
Huabin Zhang ◽  
...  

A pair of homochiral metal-organic frameworks are elaborated by employing flexible enantiopure ligands. They possess interesting double helical chains and rich hydrogen-bonding environment, exhibiting excellent chiral recognition ability to carvone.


Author(s):  
Ewa Machalska ◽  
Natalia Hachlica ◽  
Grzegorz Zajac ◽  
Davide Carraro ◽  
Malgorzata Baranska ◽  
...  

Intermolecular interactions sensitive to chirality occur in many biological events. We report a complex formation between a versatile vanadium-based probe and a chiral co-ligand monitored through the interference of electronic...


2010 ◽  
Vol 88 (4) ◽  
pp. 367-374 ◽  
Author(s):  
Kuo-xi Xu ◽  
Yu-xia Wang ◽  
Shu-yan Jiao ◽  
Jin Zhao ◽  
Chao-jie Wang

The four novel derivatives of 1,1′-bi-2-naphthol (BINOL) have been prepared, and the structures of these compounds have been characterized by IR, MS, 1H and 13C NMR spectroscopy, and elemental analysis. The enantioselective recognition of these receptors has been studied by fluorescence titration and 1H NMR spectroscopy. The receptors exhibited different chiral-recognition abilities towards some enantiomers of chiral materials and formed 1:1 complexes between host and guest. The receptors exhibit excellent enantioselective fluorescent-recognition ability towards the amino acid derivatives.


2018 ◽  
Vol 54 (21) ◽  
pp. 2643-2646 ◽  
Author(s):  
Ling Dai ◽  
Wanhua Wu ◽  
Wenting Liang ◽  
Wentong Chen ◽  
Xingke Yu ◽  
...  

γ-CD-CB[6]-cowheeled rotaxanes showed remarkably improved chiral discrimination towards chiral amines.


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