Influence of side-chain interactions on the self-assembly of discotic tricarboxyamides: a crystallographic insight

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.

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.


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.


2006 ◽  
Vol 937 ◽  
Author(s):  
Margarita Garcia ◽  
E.W. Meijer ◽  
Albertus Schenning

ABSTRACTA variety of α, α'-subtituted quaterthiophenes containing ester, amide and polymerizable side chains have been synthesized and fully characterized. The self-assembly properties of these oligothiophenes were studied as function of the side chain. Introduction of amide functionalities highly promotes the self-assembly via π-stacking and hydrogen bond interactions, while the lack of amides prevent aggregate formation. Initial experiments show that by introducing a sorbyl moiety as a polymerizable group it is possible to achieve covalent fixation of the oligothiophene units in the self-assembled state.


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.


2013 ◽  
Vol 34 (15) ◽  
pp. 1213-1219 ◽  
Author(s):  
Lisa zur Borg ◽  
Christoph Schüll ◽  
Holger Frey ◽  
Rudolf Zentel

2007 ◽  
Vol 40 (26) ◽  
pp. 9398-9405 ◽  
Author(s):  
M. Knaapila ◽  
F. B. Dias ◽  
V. M. Garamus ◽  
L. Almásy ◽  
M. Torkkeli ◽  
...  

ChemistryOpen ◽  
2017 ◽  
Vol 6 (2) ◽  
pp. 266-272 ◽  
Author(s):  
Jurgen Schill ◽  
Lech-Gustav Milroy ◽  
Jody A. M. Lugger ◽  
Albertus P. H. J. Schenning ◽  
Luc Brunsveld

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 ◽  
...  

2016 ◽  
Vol 52 (73) ◽  
pp. 10938-10947 ◽  
Author(s):  
Tomasz Marszalek ◽  
Mengmeng Li ◽  
Wojciech Pisula

This review discusses the role of chemical design on the self-assembly of donor–acceptor polymers on surfaces. Three major structural factors are highlighted including molecular weight, side chain engineering and backbone curvature of the polymers.


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.


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