Silkworm cocoons by cylinders self-assembled from H-shaped alternating polymer brushes

2015 ◽  
Vol 6 (6) ◽  
pp. 886-890 ◽  
Author(s):  
Qiutong Huang ◽  
Bo Yang ◽  
Huanhuan Liu ◽  
Youliang Zhao ◽  
Jianzhong Du

We report a novel silkworm cocoon-like nanostructure based on the 3D hierarchical self-assembly of cylinders which are spontaneously formed by an H-shaped polymer brush comprising a disulfide-bridged spacer and two brushes with alternating PEG and PCL side chains. Crystalline of PCL between adjacent cylinders bridges cylinders.

Polymers ◽  
2021 ◽  
Vol 13 (24) ◽  
pp. 4429
Author(s):  
Maria Simonova ◽  
Dmitry Ilgach ◽  
Ksenia Kaskevich ◽  
Maria Nepomnyashaya ◽  
Larisa Litvinova ◽  
...  

Novel polyfluorene polymer brushes with polymethacrylic acid side chains were obtained by atom transfer radical polymerization (ATRP) and activator generated by electron transfer (AGET) ATRP of tert-butyl methacrylate on polyfluorene multifunctional macroinitiator, followed by protonolysis of the tert-butyl groups of the side chains. Kinetics of polymerization and molecular weights were fully characterized. These polymer brushes luminesce in the blue region of the spectrum with high quantum yields (0.64–0.77). It was shown that the luminescence intensity of polymer brushes is higher than the luminescence intensity of the macroinitiator (0.61). Moreover, due to their amphiphilic nature, they can form unimolecular micelles when an alcohol solution of the polymer brush is injected into water. These properties can potentially be used in drug delivery and bioimaging.


RSC Advances ◽  
2015 ◽  
Vol 5 (113) ◽  
pp. 93337-93346 ◽  
Author(s):  
Yi Hu ◽  
Kai Miao ◽  
Bao Zha ◽  
Xinrui Miao ◽  
Li Xu ◽  
...  

This work provides efficient methods for regulating self-assembled structures by changing the position, length and odd/even properties of the side chains.


2015 ◽  
Vol 229 (7-8) ◽  
Author(s):  
Stephanie Christau ◽  
Jan Genzer ◽  
Regine von Klitzing

AbstractThis review article summarizes the progress of research in the field of polymer brush/metal nanoparticle hybrid materials. We will discuss the mutual influence of polymer brush matrix and particles. Self-assembly of particles within polymer brushes, and ways to control the loading and location of nanoparticles inside polymer brushes will be described, as well as the possibility to use the brush templates as nanoreactors to generate metal nanoparticles. The combination of stimuli-responsive polymer brushes and nanoparticles exhibiting surface plasmon resonance, such as gold or silver, enables the design of optical sensors based on reversible variations of the brush conformation. Sensing devices are capable of detecting a variety of extrinsic variations in their surrounding enviroments. The progress in the development of such optical sensors using brush/particle hybrids will be discussed in more detail.


2019 ◽  
Vol 10 (21) ◽  
pp. 2686-2696 ◽  
Author(s):  
Kohji Ohno ◽  
Shota Masuda ◽  
Hiroki Ogawa

Polymer-brush-decorated platelets produced through surface-initiated polymerization formed unique self-assembled structures in solution and in the bulk.


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.


MRS Advances ◽  
2020 ◽  
Vol 5 (64) ◽  
pp. 3507-3520
Author(s):  
Chunhui Dai ◽  
Kriti Agarwal ◽  
Jeong-Hyun Cho

AbstractNanoscale self-assembly, as a technique to transform two-dimensional (2D) planar patterns into three-dimensional (3D) nanoscale architectures, has achieved tremendous success in the past decade. However, an assembly process at nanoscale is easily affected by small unavoidable variations in sample conditions and reaction environment, resulting in a low yield. Recently, in-situ monitored self-assembly based on ion and electron irradiation has stood out as a promising candidate to overcome this limitation. The usage of ion and electron beam allows stress generation and real-time observation simultaneously, which significantly enhances the controllability of self-assembly. This enables the realization of various complex 3D nanostructures with a high yield. The additional dimension of the self-assembled 3D nanostructures opens the possibility to explore novel properties that cannot be demonstrated in 2D planar patterns. Here, we present a rapid review on the recent achievements and challenges in nanoscale self-assembly using electron and ion beam techniques, followed by a discussion of the novel optical properties achieved in the self-assembled 3D nanostructures.


2020 ◽  
Author(s):  
Daniel B. Straus ◽  
Robert J. Cava

The design of new chiral materials usually requires stereoselective organic synthesis to create molecules with chiral centers. Less commonly, achiral molecules can self-assemble into chiral materials, despite the absence of intrinsic molecular chirality. Here, we demonstrate the assembly of high-symmetry molecules into a chiral van der Waals structure by synthesizing crystals of C<sub>60</sub>(SnI<sub>4</sub>)<sub>2</sub> from icosahedral buckminsterfullerene (C<sub>60</sub>) and tetrahedral SnI4 molecules through spontaneous self-assembly. The SnI<sub>4</sub> tetrahedra template the Sn atoms into a chiral cubic three-connected net of the SrSi<sub>2</sub> type that is held together by van der Waals forces. Our results represent the remarkable emergence of a self-assembled chiral material from two of the most highly symmetric molecules, demonstrating that almost any molecular, nanocrystalline, or engineered precursor can be considered when designing chiral assemblies.


2021 ◽  
Vol 11 (7) ◽  
pp. 3254
Author(s):  
Marco Pisco ◽  
Francesco Galeotti

The realization of advanced optical fiber probes demands the integration of materials and structures on optical fibers with micro- and nanoscale definition. Although researchers often choose complex nanofabrication tools to implement their designs, the migration from proof-of-principle devices to mass production lab-on-fiber devices requires the development of sustainable and reliable technology for cost-effective production. To make it possible, continuous efforts are devoted to applying bottom-up nanofabrication based on self-assembly to decorate the optical fiber with highly ordered photonic structures. The main challenges still pertain to “order” attainment and the limited number of implementable geometries. In this review, we try to shed light on the importance of self-assembled ordered patterns for lab-on-fiber technology. After a brief presentation of the light manipulation possibilities concerned with ordered structures, and of the new prospects offered by aperiodically ordered structures, we briefly recall how the bottom-up approach can be applied to create ordered patterns on the optical fiber. Then, we present un-attempted methodologies, which can enlarge the set of achievable structures, and can potentially improve the yielding rate in finely ordered self-assembled optical fiber probes by eliminating undesired defects and increasing the order by post-processing treatments. Finally, we discuss the available tools to quantify the degree of order in the obtained photonic structures, by suggesting the use of key performance figures of merit in order to systematically evaluate to what extent the pattern is really “ordered”. We hope such a collection of articles and discussion herein could inspire new directions and hint at best practices to fully exploit the benefits inherent to self-organization phenomena leading to ordered systems.


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 143 ◽  
pp. 345 ◽  
Author(s):  
Aurelie M. Brizard ◽  
Marc C. A. Stuart ◽  
Jan H. van Esch

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