Directing the Self-Assembly of Semiconducting Copolymers: The Consequences of Grafting Linear or Hyperbranched Polyether Side Chains

2013 ◽  
Vol 34 (15) ◽  
pp. 1213-1219 ◽  
Author(s):  
Lisa zur Borg ◽  
Christoph Schüll ◽  
Holger Frey ◽  
Rudolf Zentel
Soft Matter ◽  
2021 ◽  
Author(s):  
Zhiqiang Zhao ◽  
Zheng Bian ◽  
Yu Chen ◽  
Chuanqing Kang ◽  
Lianxun Gao ◽  
...  

Chiral oligo(methylene-p-phenyleneethynylene)s can form vesicular assemblies no matter whether side chains and solvents are hydrophilic or hydrophobic. The self-assembly processes are highly independent of molecular design and chemical environments.


2009 ◽  
Vol 19 (1) ◽  
pp. 124-130 ◽  
Author(s):  
Patrick J. M. Stals ◽  
Jan F. Haveman ◽  
Rafael Martín-Rapún ◽  
Carel F. C. Fitié ◽  
Anja R. A. Palmans ◽  
...  

2017 ◽  
Vol 19 (29) ◽  
pp. 19205-19216 ◽  
Author(s):  
Yi Hu ◽  
Kai Miao ◽  
Li Xu ◽  
Bao Zha ◽  
Mengying Long ◽  
...  

We explored the chain length effect on inducing the self-assembly of diverse structures by tiny modification of the alkyl chains.


2020 ◽  
Vol 02 (01) ◽  
pp. 041-046 ◽  
Author(s):  
Yeray Dorca ◽  
Cristina Naranjo ◽  
Goutam Ghosh ◽  
Rafael Gómez ◽  
Gustavo Fernández ◽  
...  

We describe the synthesis of two propeller-shaped, emissive trisbiphenylamines 1 and (S)-2. Whilst achiral 1 forms supramolecular polymers following a cooperative mechanism, the self-assembly of chiral (S)-2 can be described by an isodesmic mechanism. Despite the isodesmic character of the supramolecular polymerization of (S)-2, an efficient transfer of chirality from the embedded point chirality of the peripheral side chains to the aggregates is demonstrated. The co-assembly of 1 and (S)-2 in a sergeants-and-soldiers experiment shows a very different dichroic response to that registered for pristine (S)-2, with a copolymerization curve displaying two transitions. Both these transitions coincide with those observed for the pristine achiral and chiral components, thus suggesting a self-sorting effect.


2016 ◽  
Vol 7 (33) ◽  
pp. 5304-5311 ◽  
Author(s):  
Dae-Yoon Kim ◽  
Dong-Gue Kang ◽  
Suyong Shin ◽  
Tae-Lim Choi ◽  
Kwang-Un Jeong

For understanding the self-assembly behaviours of norbornene-based main-chain polymers depending on side-chain pendants, a series of polynorbornenes containing the programmed dendrons is newly designed and successfully synthesized via ring opening metathesis polymerization.


RSC Advances ◽  
2015 ◽  
Vol 5 (40) ◽  
pp. 31845-31851 ◽  
Author(s):  
Arpita Paikar ◽  
Apurba Pramanik ◽  
Debasish Haldar

Side chains interactions promote the self-assembly of discotic tricarboxyamides to form an entangled fiber network and thermo responsive gel.


Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1457
Author(s):  
Manuel A. Martínez ◽  
Elisa E. Greciano ◽  
Jorge Cuéllar ◽  
José M. Valpuesta ◽  
Luis Sánchez

Herein, we describe the synthesis of highly emissive amphiphilic N-annulated PBI 1 decorated with oligo ethylene glycol (OEG) side chains. These polar side chains allow the straightforward solubility of 1 in solvents of different polarity such as water, iPrOH, dioxane, or chloroform. Compound 1 self-assembles in aqueous media by π-stacking of the aromatic units and van der Waals interactions, favored by the hydrophobic effect. The hypo- and hypsochromic effect observed in the UV-Vis spectra of 1 in water in comparison to chloroform is diagnostic of H-type aggregation. Solvent denaturation experiments allow deriving the free Gibbs energy for the self-assembly process in aqueous media and the factor m that is indicative of the influence exerted by a good solvent in the stability of the final aggregates. The ability of compound 1 to self-assemble in water yields globular aggregates that have been visualized by TEM imaging.


2012 ◽  
Vol 531-532 ◽  
pp. 640-644
Author(s):  
Xiong Yi Peng ◽  
Cong Hua Yi ◽  
Qian Qian Tang ◽  
Xue Qing Qiu

Polycarboxylate-type superplasticizers with different side chains and approximative degree of polymerization are synthesized. The microstructures of Polycarboxylate-type superplasticizers in water are studied by fluorescent probe technique, dynamic light scattering (DLS), transmission electron microscopy (TEM) and the self-assembly technique. The results indicate that the formation of hydrophobic microenvironment in PC solution is confirmed. The higher the ratio of long side chains of PC, the stronger the hydrophobic microenvironment formed in PC solution. The Z-Average diameters of aggregation formed in PC solution increase with the increasing of long side chains content. In addition, the size and shape of aggregation is not of uniform distribution, and the reason for this is that association interaction of hydrogen bonding occurs among PC molecules or in the interior of single PC molecule.


2010 ◽  
Vol 63 (4) ◽  
pp. 627 ◽  
Author(s):  
Jin Geng ◽  
Dezhi Jiao ◽  
Urs Rauwald ◽  
Oren A. Scherman

Hydrophilic copolymers containing recognition motifs based on 2-naphthol moieties in their side chains for the self-assembly with cucurbit[8]uril (CB[8]), have been prepared by reversible addition–fragmentation chain transfer polymerization. Self-assembly of the copolymer with both redox sensitive hydrophilic and hydrophobic viologen derivatives in the presence of CB[8] has been investigated.


Polymers ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 3131
Author(s):  
Naisheng Jiang ◽  
Donghui Zhang

Polypeptoids, a class of synthetic peptidomimetic polymers, have attracted increasing attention due to their potential for biotechnological applications, such as drug/gene delivery, sensing and molecular recognition. Recent investigations on the solution self-assembly of amphiphilic block copolypeptoids highlighted their capability to form a variety of nanostructures with tailorable morphologies and functionalities. Here, we review our recent findings on the solutions self-assembly of coil-crystalline diblock copolypeptoids bearing alkyl side chains. We highlight the solution self-assembly pathways of these polypeptoid block copolymers and show how molecular packing and crystallization of these building blocks affect the self-assembly behavior, resulting in one-dimensional (1D), two-dimensional (2D) and multidimensional hierarchical polymeric nanostructures in solution.


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