Graphoepitaxial Assembly of Symmetric Block Copolymers on Weakly Preferential Substrates

2010 ◽  
Vol 22 (38) ◽  
pp. 4325-4329 ◽  
Author(s):  
Eungnak Han ◽  
Huiman Kang ◽  
Chi-Chun Liu ◽  
Paul F. Nealey ◽  
Padma Gopalan
2014 ◽  
Vol 16 (19) ◽  
pp. 8865-8871 ◽  
Author(s):  
Jay Hoon Park ◽  
Yong Lak Joo

Mesoscale simulations demonstrate that nanorod inclusion in a symmetric block copolymer leads to facile formation of interconnected morphologies under cylindrical confinement.


2012 ◽  
Vol 45 (9) ◽  
pp. 3986-3992 ◽  
Author(s):  
Guoliang Liu ◽  
François Detcheverry ◽  
Abelardo Ramírez-Hernández ◽  
Hiroshi Yoshida ◽  
Yasuhiko Tada ◽  
...  

2012 ◽  
Vol 22 (16) ◽  
pp. 7672 ◽  
Author(s):  
Hiroshi Yabu ◽  
Shunsuke Sato ◽  
Takeshi Higuchi ◽  
Hiroshi Jinnai ◽  
Masatsugu Shimomura

Soft Matter ◽  
2018 ◽  
Vol 14 (8) ◽  
pp. 1389-1396 ◽  
Author(s):  
George L. Shebert ◽  
Yong Lak Joo

Using coarse-grained nonequilibrium molecular dynamics, symmetric block copolymers are simulated under the combined effects of cylindrical confinement and uniaxial extensional deformation.


Soft Matter ◽  
2020 ◽  
Vol 16 (17) ◽  
pp. 4311-4323
Author(s):  
Jingxue Zhang ◽  
Jiaping Wu ◽  
Run Jiang ◽  
Zheng Wang ◽  
Yuhua Yin ◽  
...  

The effects of chain architecture on the structural details and orientation of confined lamellae formed by symmetric AB-type block copolymer melts are studied.


2002 ◽  
Vol 724 ◽  
Author(s):  
Elizabeth R. Wright ◽  
R. Andrew McMillan ◽  
Alan Cooper ◽  
Robert P. Apkarian ◽  
Vincent P. Conticello

AbstractTriblock copolymers have traditionally been synthesized with conventional organic components. However, triblock copolymers could be synthesized by the incorporation of two incompatible protein-based polymers. The polypeptides would differ in their hydrophobicity and confer unique physiochemical properties to the resultant materials. One protein-based polymer, based on a sequence of native elastin, that has been utilized in the synthesis of biomaterials is poly (Valine-Proline-Glycine-ValineGlycine) or poly(VPGVG) [1]. This polypeptide has been shown to have an inverse temperature transition that can be adjusted by non-conservative amino acid substitutions in the fourth position [2]. By combining polypeptide blocks with different inverse temperature transition values due to hydrophobicity differences, we expect to produce amphiphilic polypeptides capable of self-assembly into hydrogels. Our research examines the design, synthesis and characterization of elastin-mimetic block copolymers as functional biomaterials. The methods that are used for the characterization include variable temperature 1D and 2D High-Resolution-NMR, cryo-High Resolutions Scanning Electron Microscopy and Differential Scanning Calorimetry.


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