Nanoparticle-Driven Assembly of Block Copolymers: A Simple Route to Ordered Hybrid Materials

2011 ◽  
Vol 133 (17) ◽  
pp. 6513-6516 ◽  
Author(s):  
Ying Lin ◽  
Vikram K. Daga ◽  
Eric R. Anderson ◽  
Samuel P. Gido ◽  
James J. Watkins

2000 ◽  
Vol 72 (1-2) ◽  
pp. 67-72 ◽  
Author(s):  
Keith J. Watson ◽  
Jin Zhu ◽  
SonBinh T. Nguyen ◽  
Chad A. Mirkin

Ring-opening metathesis polymerization was used to modify organic soluble gold nanoparticles with redox-active polymers. A gel-permeation chromatography study revealed that each nanoparticle is modified with approximately 11 polymer chains. Electrochemical studies of nanoparticles modified with block copolymers of two different redox-active groups revealed that each monomer is electrochemically accessible, while no current rectification was observed.





2019 ◽  
Vol 10 (6) ◽  
pp. 1746-1753 ◽  
Author(s):  
Sergio Ayala ◽  
Kyle C. Bentz ◽  
Seth M. Cohen

Block copolymers were used to generate metal–organic frameworks (MOFs) as novel materials (block co-polyMOFs, BCPMOFs) with controlled morphologies.



2001 ◽  
pp. 1116-1117 ◽  
Author(s):  
Robert J. P. Corriu ◽  
Frank Embert ◽  
Yannick Guari ◽  
Ahmad Mehdi ◽  
Catherine Reyé


1999 ◽  
Vol 5 (S2) ◽  
pp. 628-629
Author(s):  
Alexander Du Chesne ◽  
Ralph Ulrich ◽  
Ulrich Wiesner

A topic of growing importance is the nano-structuring of inorganic materials by exploiting interactions with self assembling polymers. One example are multiphase polymers.Driven by the mixing enthalpy, most polymers phase separate below their critical solution temperature. The components of block copolymers are covalently linked, restricting separation to microscopic length scales. Depending on composition, block copolymers form different equilibrium morphologies representing the energetically most favorable balance between- interfacial area and chain conformation.Mass thickness contrast of polymers is often weak and conventional TEM can thus fail to characterize the morphology unless selective staining methods exist. This is the case for the poly(isoprene)-b-poly(ethyleneoxide) diblock copolymer system (PI-b-PEO) used as a structure directing agent and to provide solubility (see below). Fig. 1 shows the micro-domain morphology of PI-b-PEO where the rubbery phase is selectively stained with OsO4 .Hybrid materials are obtained by addition of an inorganic precursor to a solution of PI-b-PEO in a "mutual" solvent.



2015 ◽  
Vol 6 (17) ◽  
pp. 3236-3244 ◽  
Author(s):  
Trevor Gavin Wright ◽  
Harald Pasch

For the first time, deuterated polystyrene block copolymers were synthesized by RITP and analysed by advanced fractionation and spectroscopic methods.



2017 ◽  
Vol 46 (3) ◽  
pp. 569-585 ◽  
Author(s):  
Dechao Niu ◽  
Yongsheng Li ◽  
Jianlin Shi

Silica/organosilica cross-linked block copolymer micelles are a novel class of hybrid materials that combine the advantages of amphiphilic block copolymers and silica/organosilica cross-linking agents into one unit. This Tutorial Review summarizes the recent progress in the design, synthesis and biomedical applications of various silica/organosilica cross-linked block copolymer micelles.



2016 ◽  
Vol 69 (7) ◽  
pp. 701 ◽  
Author(s):  
Lauren J. Kang ◽  
Christine K. Luscombe

End-functionalized poly(3-hexylthiophene) (P3HT) has contributed to continued advancements in conjugated polymer applications, especially within organic electronics. P3HT synthesized using Kumada catalyst-transfer polymerization (KCTP) has many favourable attributes such as controlled molecular weight, high regioregularity, and narrow dispersity. With the addition of reactive end-groups, P3HT plays an important role in advancing the development of hybrid materials and preparation of block copolymers. Exploring methods of end-functionalization that result in heteroatom-bond formation, giving a non-carbon atom bonded to the terminal thiophene, could help control and understand the p–n junction of hybrid materials. This research highlight focuses on the development of a novel and facile way of end-functionalizing P3HT with chalcogens.



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