Understanding the self-assembly pathways of a single chain variant of monellin: A first step towards the design of sweet nanomaterials

2020 ◽  
Vol 152 ◽  
pp. 21-29
Author(s):  
Masoud Delfi ◽  
Serena Leone ◽  
Alessandro Emendato ◽  
Diletta Ami ◽  
Margherita Borriello ◽  
...  
2021 ◽  
Author(s):  
Wei Wen ◽  
Aihua Chen

Self-assembly of amphiphilic single chain Janus nanoparticles (SCJNPs) is a novel and promising approach to fabricate assemblies with diversified morphologies. However, the experimental research of the self-assembly behavior of SCJNPs...


Soft Matter ◽  
2020 ◽  
Vol 16 (42) ◽  
pp. 9738-9745
Author(s):  
Beatriz Robles-Hernández ◽  
Edurne González ◽  
José A. Pomposo ◽  
Juan Colmenero ◽  
Ángel Alegría

Dielectric studies on water dynamics in aqueous solutions of amphiphilic random copolymers confirm the self-assembly into globular like core–shell single-chain nano-particles (SCNPs) at concentrations well above the overlap concentration.


2019 ◽  
Vol 2 (1) ◽  
Author(s):  
Leonardo Hayato Foianesi-Takeshige ◽  
Satoshi Takahashi ◽  
Tomoki Tateishi ◽  
Ryosuke Sekine ◽  
Atsushi Okazawa ◽  
...  

Abstract The template effect is a key feature to control the arrangement of building blocks in assemblies, but its kinetic nature remains elusive compared to the thermodynamic aspects, with the exception of very simple reactions. Here we report a kinetic template effect in a self-assembled cage composed of flexible ditopic ligands and Pd(II) ions. Without template anion, a micrometer-sized sheet is kinetically trapped (off-pathway), which is converted into the thermodynamically most stable cage by the template anion. When the template anion is present from the start, the cage is selectively produced by the preferential cyclization of a dinuclear intermediate (on-pathway). Quantitative and numerical analyses of the self-assembly of the cage on the on-pathway revealed that the accelerating effect of the template is stronger for the early stage reactions of the self-assembly than for the final cage formation step itself, indicating the kinetic template effect.


2016 ◽  
Vol 110 (3) ◽  
pp. 170a
Author(s):  
Hsien-Shun Liao ◽  
Peng Huang ◽  
Yuan Gao ◽  
Edward Cai ◽  
Ferenc Horkay ◽  
...  

Soft Matter ◽  
2012 ◽  
Vol 8 (30) ◽  
pp. 7865 ◽  
Author(s):  
Mengying Xiao ◽  
Guangjie Xia ◽  
Rong Wang ◽  
Daiqian Xie

2004 ◽  
Vol 87 (6) ◽  
pp. 3648-3656 ◽  
Author(s):  
Guanghong Wei ◽  
Normand Mousseau ◽  
Philippe Derreumaux

2020 ◽  
Vol 56 (89) ◽  
pp. 13808-13811
Author(s):  
Ingo Helmers ◽  
Nils Bäumer ◽  
Gustavo Fernández

In this work, we unravel the impact of hydrophobic domain flexibility on the self-assembly pathways and aggregate morphology of amphiphilic systems in aqueous media.


Molecules ◽  
2020 ◽  
Vol 25 (17) ◽  
pp. 4033
Author(s):  
Enrique Folgado ◽  
Matthias Mayor ◽  
Vincent Ladmiral ◽  
Mona Semsarilar

To date, amphiphilic block copolymers (BCPs) containing poly(vinylidene fluoride-co-hexafluoropropene) (P(VDF-co-HFP)) copolymers are rare. At moderate content of HFP, this fluorocopolymer remains semicrystalline and is able to crystallize. Amphiphilic BCPs, containing a P(VDF-co-HFP) segment could, thus be appealing for the preparation of self-assembled block copolymer morphologies through crystallization-driven self-assembly (CDSA) in selective solvents. Here the synthesis, characterization by 1H and 19F NMR spectroscopies, GPC, TGA, DSC, and XRD; and the self-assembly behavior of a P(VDF-co-HFP)-b-PEG-b-P(VDF-co-HFP) triblock copolymer were studied. The well-defined ABA amphiphilic fluorinated triblock copolymer was self-assembled into nano-objects by varying a series of key parameters such as the solvent and the non -solvent, the self-assembly protocols, and the temperature. A large range of morphologies such as spherical, square, rectangular, fiber-like, and platelet structures with sizes ranging from a few nanometers to micrometers was obtained depending on the self-assembly protocols and solvents systems used. The temperature-induced crystallization-driven self-assembly (TI-CDSA) protocol allowed some control over the shape and size of some of the morphologies.


Nanoscale ◽  
2018 ◽  
Vol 10 (3) ◽  
pp. 1508-1516 ◽  
Author(s):  
Nikola A. Dudukovic ◽  
Benjamin C. Hudson ◽  
Anant K. Paravastu ◽  
Charles F. Zukoski

The effects of solvent–solute interactions on the self-assembly of a dipeptide molecule into nanofibers are explored.


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