ChemInform Abstract: Synthetic Macrocyclic Receptors: From Molecular Recognition to Supramolecular Functions

ChemInform ◽  
2001 ◽  
Vol 32 (19) ◽  
pp. no-no
Author(s):  
Rocco Ungaro
2006 ◽  
Vol 235 (1) ◽  
pp. 39-51 ◽  
Author(s):  
Edward A. Karakhanov ◽  
Lyusyen M. Karapetyan ◽  
Yulia S. Kardasheva ◽  
Anton L. Maksimov ◽  
Elena A. Runova ◽  
...  

1992 ◽  
Vol 5 (10) ◽  
pp. 633-643 ◽  
Author(s):  
Jun-Ichi Kikuchi ◽  
Chiemi Matsushima ◽  
Yumi Tanaka ◽  
Ken-Ichi Hie ◽  
Kazuaki Suehiro ◽  
...  

1995 ◽  
Vol 117 (50) ◽  
pp. 12416-12425 ◽  
Author(s):  
Masahiko Inouye ◽  
Toshiyuki Miyake ◽  
Masaru Furusyo ◽  
Hiroyuki Nakazumi

ChemInform ◽  
2006 ◽  
Vol 37 (37) ◽  
Author(s):  
Edward A. Karakhanov ◽  
Lyusyen M. Karapetyan ◽  
Yulia S. Kardasheva ◽  
Anton L. Maksimov ◽  
Elena A. Runova ◽  
...  

RSC Advances ◽  
2014 ◽  
Vol 4 (91) ◽  
pp. 49663-49671
Author(s):  
Shyamaprosad Goswami ◽  
Rinku Chakrabarty ◽  
Swapan Dey ◽  
Hoong-Kun Fun

The ditopic macrocyclic receptors having NO2 group show inhibition in hydrogen bonding molecular recognition towards the dicarboxylic acids to behave as monotopic receptors.


2018 ◽  
Vol 47 (18) ◽  
pp. 7006-7026 ◽  
Author(s):  
Roberta Pinalli ◽  
Alessandro Pedrini ◽  
Enrico Dalcanale

This review summarizes recent developments in biochemical sensing using macrocyclic receptors, from molecular recognition to device fabrication and testing.


2020 ◽  
Author(s):  
Junxia Ren ◽  
Yaozu Liu ◽  
Xin Zhu ◽  
Yangyang Pan ◽  
Yujie Wang ◽  
...  

<p><a></a><a></a><a></a><a></a><a></a><a></a><a></a><a>The development of highly-sensitive recognition of </a><a></a><a></a><a></a><a></a><a>hazardous </a>chemicals, such as volatile organic compounds (VOCs) and polycyclic aromatic hydrocarbons (PAHs), is of significant importance because of their widespread social concerns related to environment and human health. Here, we report a three-dimensional (3D) covalent organic framework (COF, termed JUC-555) bearing tetraphenylethylene (TPE) side chains as an aggregation-induced emission (AIE) fluorescence probe for sensitive molecular recognition.<a></a><a> </a>Due to the rotational restriction of TPE rotors in highly interpenetrated framework after inclusion of dimethylformamide (DMF), JUC-555 shows impressive AIE-based strong fluorescence. Meanwhile, owing to the large pore size (11.4 Å) and suitable intermolecular distance of aligned TPE (7.2 Å) in JUC-555, the obtained material demonstrates an excellent performance in the molecular recognition of hazardous chemicals, e.g., nitroaromatic explosives, PAHs, and even thiophene compounds, via a fluorescent quenching mechanism. The quenching constant (<i>K</i><sub>SV</sub>) is two orders of magnitude better than those of other fluorescence-based porous materials reported to date. This research thus opens 3D functionalized COFs as a promising identification tool for environmentally hazardous substances.</p>


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