Modulating the self-assembly of rigid “clicked” dendrimers at the solid–liquid interface by tuning non-covalent interactions between side groups

2011 ◽  
Vol 47 (38) ◽  
pp. 10578 ◽  
Author(s):  
Andrea Cadeddu ◽  
Artur Ciesielski ◽  
Tamer El Malah ◽  
Stefan Hecht ◽  
Paolo Samorì
Langmuir ◽  
2008 ◽  
Vol 24 (17) ◽  
pp. 9566-9574 ◽  
Author(s):  
Mathieu Linares ◽  
Patrizia Iavicoli ◽  
Krystallia Psychogyiopoulou ◽  
David Beljonne ◽  
Steven De Feyter ◽  
...  

2015 ◽  
Vol 51 (58) ◽  
pp. 11677-11680 ◽  
Author(s):  
Mohamed El Garah ◽  
Rosaria C. Perone ◽  
Alejandro Santana Bonilla ◽  
Sébastien Haar ◽  
Marilena Campitiello ◽  
...  

The self-assembly of three novel lipophilic guanosine derivatives at the solid/liquid interface lead to the generation of either G-ribbons, lamellar G-dimer arrays or the G4 cation-free architectures.


2018 ◽  
Vol 54 (73) ◽  
pp. 10264-10267 ◽  
Author(s):  
Bart Stel ◽  
Fernando Cometto ◽  
Behzad Rad ◽  
James J. De Yoreo ◽  
Magalí Lingenfelder

Kinetic pathway in S-layer self-assembly at the solid–liquid interface across time (second to hours) and spatial scales (nm to microns).


2001 ◽  
Vol 123 (46) ◽  
pp. 11462-11467 ◽  
Author(s):  
Paolo Samorí ◽  
Andreas Fechtenkötter ◽  
Frank Jäckel ◽  
Thilo Böhme ◽  
Klaus Müllen ◽  
...  

2021 ◽  
Author(s):  
Cui-Lian Liu ◽  
Eduard Bobylev ◽  
Brice Kauffmann ◽  
Koen Robeyns ◽  
Yann Garcia ◽  
...  

Non-covalent interactions play an essential role in the folding and self-assembly of large biological assemblies. These interactions are not only a driving force for the formation of large structures but also control conformation and com-plementary shapes of subcomponents that promote the diversity of structures and functions of the resulting assemblies. Understanding how non-covalent interactions direct self-assembly and the effect of conformation and complementary shapes on self-assembled structures will help design artificial supramolecular systems with extended components and functions. Herein, we develop a strategy for controlling more complex self-assembly with lower symmetry and flexible building blocks that combine endohedral non-covalent interactions with a dual curvature in the ligand backbone to give additional shape complementarity. A Diels-Alder reaction was used to break the symmetry of the diazaanthracene units of the ligands to give dual curvature ligands with different shapes and endohedral groups (L1-L3). The self-assembly studies of these ligands demonstrated that non-covalent interactions and shape complementary effectively control the self-assembly and enable the design of cages for supramolecular catalysis.


2012 ◽  
Vol 18 (10) ◽  
pp. 3056-3063 ◽  
Author(s):  
Javier Saiz-Poseu ◽  
Jordi Faraudo ◽  
Antoni Figueras ◽  
Ramon Alibes ◽  
Felix Busqué ◽  
...  

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