Synthesis and Solution Self-Assembly of Side-Chain Cobaltocenium-Containing Block Copolymers

2010 ◽  
Vol 132 (26) ◽  
pp. 8874-8875 ◽  
Author(s):  
Lixia Ren ◽  
Christopher G. Hardy ◽  
Chuanbing Tang
2020 ◽  
Vol 11 (45) ◽  
pp. 7147-7158
Author(s):  
Bret M. Boyle ◽  
Joseph L. Collins ◽  
Tara E. Mensch ◽  
Matthew D. Ryan ◽  
Brian S. Newell ◽  
...  

Four series of brush block copolymers with near identical side chain compositions but varying backbone structures were synthesized to investigate the effect of backbone structure on the thermal self-assembly to photonic crystals.


Soft Matter ◽  
2012 ◽  
Vol 8 (5) ◽  
pp. 1460-1466 ◽  
Author(s):  
Huifeng Ren ◽  
Yaoting Wu ◽  
Ning Ma ◽  
Huaping Xu ◽  
Xi Zhang

2016 ◽  
Vol 99 ◽  
pp. 26-34 ◽  
Author(s):  
Sudhansu Sekhar Jena ◽  
Saswati Ghosh Roy ◽  
Venkanna Azmeera ◽  
Priyadarsi De

2008 ◽  
Vol 41 (1) ◽  
pp. 218-229 ◽  
Author(s):  
Manas Shah ◽  
Victor Pryamitsyn ◽  
Venkat Ganesan

2013 ◽  
Vol 46 (20) ◽  
pp. 8245-8252 ◽  
Author(s):  
Prashant Deshmukh ◽  
Suk-kyun Ahn ◽  
Ludovic Geelhand de Merxem ◽  
Rajeswari M. Kasi

2020 ◽  
Vol 11 (6) ◽  
pp. 1237-1248 ◽  
Author(s):  
Davy Daubian ◽  
Jens Gaitzsch ◽  
Wolfgang Meier

A new PEO-b-PEHOx amphiphilic diblock copolymer was achieved which unlocked new complex self-assembled structures. Thanks to its hydrophobic oxazoline block with a long branched side chain, EHOx, various potent structures were obtained.


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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