Fabrication of size-controllable mPEG-decorated microparticles conjugating optically active ketoprofen based on self-assembly of amphiphilic random copolymers

2012 ◽  
Vol 127 (4) ◽  
pp. 3242-3248 ◽  
Author(s):  
Xia Li ◽  
Guo-Jun Zhou ◽  
Guo-Hai Chu ◽  
Xian-Fu Lin ◽  
Jun-Liang Wang ◽  
...  
2000 ◽  
Vol 33 (10) ◽  
pp. 3671-3679 ◽  
Author(s):  
Gabino A. Carriedo ◽  
Francisco J. García Alonso ◽  
Paloma Gómez Elipe ◽  
José L. García-Alvarez ◽  
M. Pilar Tarazona ◽  
...  

2020 ◽  
Vol 20 (4) ◽  
pp. 6-26
Author(s):  
V. A. Burmistrov ◽  
V. V. Aleksandriiskii ◽  
I. V. Novikov ◽  
O. I. Koifman

Induction of helical mesophases by incorporating chiral dopants into the nematics matrix is the promising modern trends in the chemistry of liquid crystals. This process is associated with a unique phenomenon - an amplification of chirality in liquid-crystalline phases, which ensures the detection of enantiomers by their chiral induction, much more sensitive than other methods. The relevance of this approach is due to the need to create perspective electro-optical devices operating with ultra-low control voltages based on twist effects, chromatographic stationary phases with high chiral selectivity, flexible magnets, photo-sensitive nanostructures, and other smart LC materials. The successful solution of these problems is impossible without experimental research and theoretical comprehension of the mechanisms of third level chiral transfer optically active dopant – nematic liquid crystal. In the last decade, a large number of works have appeared on the solution of these problems. This review is devoted to a generalization of the experimental results and a theoretical description of the transfer of molecular chirality to orientationally ordered systems with the participation of both chiral molecular substituents with an asymmetric carbon atom and planar or quasi-planar fragments chirally distorted relative to each other. The stereochemical aspects of induction associated with the structural correspondences of the dopant and nematic liquid crystal, as well as the main classes of optically active additives, are discussed. Application of metal complexes, both Werner and macroheterocyclic, are presented. Special attention is paid to the results of the mechanisms study of chiral transfer due to various intermolecular interactions: hydrogen bonding, axial coordination, and the formation of inclusion compounds. The high efficiency of induction of spiral mesophases has been demonstrated with a combination of different self-assembly mechanisms in liquid crystal - chiral additive systems.


2000 ◽  
Vol 661 ◽  
Author(s):  
Shirish M. Chitanvis

We have mapped the physics of a system of random copolymers onto a time-dependent density functional-type field theory using techniques of functional integration. Time in the theory is merely a label for the location of a given monomer along the extent of a flexible chain. We derive heuristically within this approach a non-local constraint which prevents segments on chains in the system from straying too far from each other, and leads to self-assembly. The structure factor is then computed in a straightforward fashion. The dependence of various calculated quantities on the average chain length are compared with experiments. The profile and size of spherulitic mesoscale domains is also computed.


2018 ◽  
Vol 51 (2) ◽  
pp. 398-409 ◽  
Author(s):  
Shota Imai ◽  
Yuji Hirai ◽  
Chitose Nagao ◽  
Mitsuo Sawamoto ◽  
Takaya Terashima

Soft Matter ◽  
2020 ◽  
Vol 16 (42) ◽  
pp. 9738-9745
Author(s):  
Beatriz Robles-Hernández ◽  
Edurne González ◽  
José A. Pomposo ◽  
Juan Colmenero ◽  
Ángel Alegría

Dielectric studies on water dynamics in aqueous solutions of amphiphilic random copolymers confirm the self-assembly into globular like core–shell single-chain nano-particles (SCNPs) at concentrations well above the overlap concentration.


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