scholarly journals Self-assembly of small molecules at hydrophobic interfaces using group effect

Nanoscale ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 5452-5463 ◽  
Author(s):  
William Foster ◽  
Keisuke Miyazawa ◽  
Takeshi Fukuma ◽  
Halim Kusumaatmaja ◽  
Kislon Voϊtchovsky

Group effect allows non-tethered small molecules to form a wide variety of self-assembled structures at solid–liquid interfaces.

Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1502
Author(s):  
Johannes M. Parikka ◽  
Karolina Sokołowska ◽  
Nemanja Markešević ◽  
J. Jussi Toppari

The predictable nature of deoxyribonucleic acid (DNA) interactions enables assembly of DNA into almost any arbitrary shape with programmable features of nanometer precision. The recent progress of DNA nanotechnology has allowed production of an even wider gamut of possible shapes with high-yield and error-free assembly processes. Most of these structures are, however, limited in size to a nanometer scale. To overcome this limitation, a plethora of studies has been carried out to form larger structures using DNA assemblies as building blocks or tiles. Therefore, DNA tiles have become one of the most widely used building blocks for engineering large, intricate structures with nanometer precision. To create even larger assemblies with highly organized patterns, scientists have developed a variety of structural design principles and assembly methods. This review first summarizes currently available DNA tile toolboxes and the basic principles of lattice formation and hierarchical self-assembly using DNA tiles. Special emphasis is given to the forces involved in the assembly process in liquid-liquid and at solid-liquid interfaces, and how to master them to reach the optimum balance between the involved interactions for successful self-assembly. In addition, we focus on the recent approaches that have shown great potential for the controlled immobilization and positioning of DNA nanostructures on different surfaces. The ability to position DNA objects in a controllable manner on technologically relevant surfaces is one step forward towards the integration of DNA-based materials into nanoelectronic and sensor devices.


2017 ◽  
Vol 8 (2) ◽  
pp. 1350-1355 ◽  
Author(s):  
Alexander S. Groombridge ◽  
Aniello Palma ◽  
Richard M. Parker ◽  
Chris Abell ◽  
Oren A. Scherman

The successful self-assembly of a stimuli-responsive aqueous supramolecular hyperbranched polymer from small molecules and the macrocyclic host cucurbit[8]uril (CB[8]) is reported. This self-healing supramolecular network can act as a soft matter barrier at liquid–liquid interfaces.


Langmuir ◽  
2016 ◽  
Vol 33 (1) ◽  
pp. 372-381 ◽  
Author(s):  
Roozbeh Hajiraissi ◽  
Ignacio Giner ◽  
Guido Grundmeier ◽  
Adrian Keller

Nanoscale ◽  
2018 ◽  
Vol 10 (7) ◽  
pp. 3438-3443 ◽  
Author(s):  
Zhen-Feng Cai ◽  
Hui-Juan Yan ◽  
Dong Wang ◽  
Li-Jun Wan

We report the potential and concentration controlled assembly of an alkyl-substituted benzo[1,2-b:4,5-b′]dithiophene (DDBDT) on an Au(111) electrode byin situelectrochemical scanning tunneling microscopy (ECSTM).


2020 ◽  
pp. 1905784
Author(s):  
Shuai Zhang ◽  
Jiajun Chen ◽  
Jianli Liu ◽  
Harley Pyles ◽  
David Baker ◽  
...  

Langmuir ◽  
2002 ◽  
Vol 18 (21) ◽  
pp. 8085-8095 ◽  
Author(s):  
Orlando J. Rojas ◽  
Lubica Macakova ◽  
Eva Blomberg ◽  
Åsa Emmer ◽  
Per M. Claesson

2021 ◽  
Vol 2116 (1) ◽  
pp. 012042
Author(s):  
Kenny Yu ◽  
Ryan Enright ◽  
David McCloskey

Abstract A Monte Carlo method, implemented for quantifying confidence bounds on thermoreflectance (TR) measurements of interfacial thermal conductance G at solid-liquid interfaces modified with self-assembled monolayers (SAMs) is presented in this paper. Here we used 1-decanethiol (1DT) and 1H,1H,2H,2H-Perfluorodecanethiol (PFDT) SAMs to achieve two distinct work of adhesion. Using TR measurements in conjunction with Monte Carlo simulations, we determined G values to be 51 ± 7 MWm-2K-1, 58 ± 8 MWm-2K-1, and 72 ± 17 MWm-2K-1 for Au-PFDT-H2O, Au-1DT-H2O, and Au-H2O, respectively. Our results with the new confidence bounds position our experimental data on surfaces modified with SAMs comparable to literature. However, contrary to previous results shown in the literature, our data showed that a significant decrease in G can be seen for DI water on bare Au that was exposed in ambient for extended period. Our results indicate that G could be influenced by factors beyond a simple work of adhesion, an indication also seen from the work of Park et al.. To solidify this finding, further investigation is necessary to better understand G dependence on surface wettability.


Soft Matter ◽  
2014 ◽  
Vol 10 (15) ◽  
pp. 2612 ◽  
Author(s):  
Jinhua Cai ◽  
Haihui Chen ◽  
Jiangen Huang ◽  
Jingxia Wang ◽  
Dongliang Tian ◽  
...  

2015 ◽  
Vol 45 (4) ◽  
pp. 331-339 ◽  
Author(s):  
Sagheer A. Onaizi ◽  
M. S. Nasser ◽  
Nasir M. A. Al-Lagtah

Sign in / Sign up

Export Citation Format

Share Document