Entropy-Driven Hierarchical Nanostructures from Cooperative Self-Assembly of Gold Nanoparticles/Block Copolymers under Three-Dimensional Confinement

2015 ◽  
Vol 48 (16) ◽  
pp. 5980-5987 ◽  
Author(s):  
Nan Yan ◽  
Hongxia Liu ◽  
Yutian Zhu ◽  
Wei Jiang ◽  
Zeyuan Dong
Nanoscale ◽  
2017 ◽  
Vol 9 (39) ◽  
pp. 15056-15061 ◽  
Author(s):  
Yun He ◽  
Yan Zhang ◽  
Nan Yan ◽  
Yutian Zhu ◽  
Wei Jiang ◽  
...  

The unique sieve-like particles with lattice arrayed switchable channels were created via the confined self-assembly of P4VP-b-PS-b-P4VP triblock copolymers within the emulsion droplets.


Molecules ◽  
2019 ◽  
Vol 24 (9) ◽  
pp. 1772 ◽  
Author(s):  
Maria de los Angeles Cortes ◽  
Raquel de la Campa ◽  
Maria Luisa Valenzuela ◽  
Carlos Díaz ◽  
Gabino A. Carriedo ◽  
...  

During the last number of years a variety of crystallization-driven self-assembly (CDSA) processes based on semicrystalline block copolymers have been developed to prepare a number of different nanomorphologies in solution (micelles). We herein present a convenient synthetic methodology combining: (i) The anionic polymerization of 2-vinylpyridine initiated by organolithium functionalized phosphane initiators; (ii) the cationic polymerization of iminophosphoranes initiated by –PR2Cl2; and (iii) a macromolecular nucleophilic substitution step, to prepare the novel block copolymers poly(bistrifluoroethoxy phosphazene)-b-poly(2-vinylpyridine) (PTFEP-b-P2VP), having semicrystalline PTFEP core forming blocks. The self-assembly of these materials in mixtures of THF (tetrahydrofuran) and 2-propanol (selective solvent to P2VP), lead to a variety of cylindrical micelles of different lengths depending on the amount of 2-propanol added. We demonstrated that the crystallization of the PTFEP at the core of the micelles is the main factor controlling the self-assembly processes. The presence of pyridinyl moieties at the corona of the micelles was exploited to stabilize gold nanoparticles (AuNPs).


2010 ◽  
Vol 23 (5) ◽  
pp. 634-639 ◽  
Author(s):  
Jeong Gon Son ◽  
Adam F. Hannon ◽  
Kevin W. Gotrik ◽  
Alfredo Alexander-Katz ◽  
Caroline A. Ross

2006 ◽  
Vol 110 (6) ◽  
pp. 2798-2803 ◽  
Author(s):  
Ahmed I. Abdelrahman ◽  
Ahmad M. Mohammad ◽  
Takeyoshi Okajima ◽  
Takeo Ohsaka

2011 ◽  
Vol 44 (15) ◽  
pp. 5868-5873 ◽  
Author(s):  
Hiroshi Yabu ◽  
Tatsuya Jinno ◽  
Kazutaka Koike ◽  
Takeshi Higuchi ◽  
Masatsugu Shimomura

2014 ◽  
Vol 1706 ◽  
Author(s):  
Hiroaki Wakayama ◽  
Hirotaka Yonekura ◽  
Yasuaki Kawai

ABSTRACTPeriodically ordered nanohetero inorganic structures offer great promise due to their unique electric, ionic, magnetic, and photonic properties. Many studies have focused on the formation of periodically ordered nano-hetero inorganic structures through layer-by-layer adsorption, sputtering, and self-assembly methods. However, the construction of three-dimensional periodically ordered nanohetero inorganic structures with desired sizes and morphologies remains a great challenge. We present a simple method for producing three-dimensional periodically ordered inorganic nanoheterostructures with controlled shape and size by replicating self-assembled block copolymers (BCPs) containing precursors of metals and metal oxides. Precursors were dissolved with BCPs in a solvent. Upon evaporation of the solvent, each precursor was selectively introduced into a separate polymer block. Application of an external magnetic field (10 T) to the BCP-precursor composites resulted in a phase transition of from spheres to hexagonal cylinders. Subsequent pyrolytic removal of the BCPs produced periodically ordered nanoheterostructures that were structural replicates of the precursor–BCP composites. Self-assembled nano-hetero inorganic structures of nanoparticles, nanorods and layers in a matrix were produced. The morphology and domain size can be tailored by controlling the molecular weight and relative block length of block copolymers. The controlled size and morphology of the inorganic nanoheterostructures demonstrate the method’s utility for producing highly functional materials.


2019 ◽  
Vol 10 (34) ◽  
pp. 4637-4642 ◽  
Author(s):  
Anna P. Constantinou ◽  
Uriel Marie-Sainte ◽  
Lihui Peng ◽  
Dean R. Carroll ◽  
Catriona M. McGilvery ◽  
...  

Gold nanoparticles (AuNPs) fabricated via the self-assembly of block copolymers of various architectures.


2015 ◽  
Vol 3 (9) ◽  
pp. 1169-1175 ◽  
Author(s):  
Dong-Po Song ◽  
Cheng Li ◽  
Nicholas S. Colella ◽  
Xuemin Lu ◽  
Jae-Hwang Lee ◽  
...  

Author(s):  
Song J

Plasmonic assemblies of gold nanoparticles (AuNPs) triggered by DNA exhibited excellent biocompatibility and specific-targeting ability. Moreover, the integration of AuNPs and DNA allows the DNA scaffolds exhibit greater chemical stability and optical plasmonic properties. In this mini review, we summarized the development of DNA nanotechnology, especially DNA framework and DNA origami that were employed to fabricate two-dimensional and three-dimensional (3D) Au nanoassembled nanostructures.


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