scholarly journals Self-assembly of diphenylalanine with preclick components as capping groups

2017 ◽  
Vol 19 (39) ◽  
pp. 27038-27051 ◽  
Author(s):  
Andrea Gemma ◽  
Enric Mayans ◽  
Gema Ballano ◽  
Juan Torras ◽  
Angélica Díaz ◽  
...  

Alkyne and azide, which are commonly used in the cycloaddition reaction recognized as “click chemistry”, have been used as capping groups of two engineered diphenylalanine (FF) derivatives due to their ability to form weak intermolecular interactions (i.e. dipole–π and π–π stacking).

2010 ◽  
Vol 39 (32) ◽  
pp. 7534 ◽  
Author(s):  
Eric Besson ◽  
Ahmad Mehdi ◽  
Catherine Reyé ◽  
Philippe Gaveau ◽  
Robert J. P. Corriu

2014 ◽  
Vol 2 (39) ◽  
pp. 8285-8294 ◽  
Author(s):  
Alexander N. Chernyshev ◽  
Dmitry Morozov ◽  
Jarkko Mutanen ◽  
Vadim Yu Kukushkin ◽  
Gerrit Groenhof ◽  
...  

In this work we demonstrate that protonation and π-stacking can be exploited to convert non-luminescent 2,2′-dipyridylamine into blue-emitting derivatives.


2010 ◽  
Vol 63 (8) ◽  
pp. 1169 ◽  
Author(s):  
Robert Chapman ◽  
Katrina A. Jolliffe ◽  
Sébastien Perrier

Self-assembling cyclic peptide-polymer conjugates were prepared by ‘clicking’ polymers (prepared by RAFT polymerization) to an azide functionalized d-alt-l cyclic octapeptide via the Huisgen 1,3-dipolar cycloaddition reaction. Due to the high graft density, the efficiency of the click chemistry conjugation reaction was found to be highly dependent on the size of the polymer. At relatively low molecular weights, as many as four polymer chains could be grafted to each 8 residue cyclic peptide ring. Evidence for the self assembly of the conjugates into peptide-polymer nanotubes was observed by TEM and IR.


Author(s):  
Sathish Chatnahalli Gangadharappa ◽  
Iván Maisuls ◽  
Ileana P. Salto ◽  
Silke Niemann ◽  
Viktoria Bachtin ◽  
...  

2021 ◽  
Vol 57 (3) ◽  
pp. 266-273
Author(s):  
Kyrill Yu. Suponitsky ◽  
Aleksei A. Anisimov ◽  
Ivan V. Ananyev ◽  
Alexander A. Lashakov ◽  
Svetlana V. Osintseva ◽  
...  

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