## Abstract We report a simulated annealing study of the self‐assembly of symmetric lamella‐forming ABA triblock copolymers confined in cylindrical nanopores. We systematically examine the dependence of the self‐assembled morphologies and structural parameters on the degree of confinement and the s
Self-Assembly of Cylinder-Forming ABA Triblock Copolymers under Cylindrical Confinement
✍ Scribed by Zheng Wang; Baohui Li; Qinghua Jin; Datong Ding; An-Chang Shi
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 424 KB
- Volume
- 17
- Category
- Article
- ISSN
- 1022-1344
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The self‐assembly of two types of linear ABA triblock copolymers confined in cylindrical nanopores is studied using simulated annealing. The effects of pore size and block copolymer chain architecture on morphology, chain conformations and bridging fraction are investigated. For the bulk cylinder‐forming copolymers, novel structures such as helices and stacked toroids form, which depend sensitively on the pore size. Several significant differences between the two types of copolymers are predicted and explained based on the differences in their chain conformations and chain architectures. A simple model is proposed to explain the mean square radius of gyration for the bridge and loop chains.
magnified image
📜 SIMILAR VOLUMES
## Abstract Monte Carlo simulations were used to identify the microphase morphologies of ABA triblock copolymer melts confined in a cylindrical nanotube. The influences of the volume fraction of mid‐block B (__f__~B~), the radius of nanotube (__R__) and the asymmetry of ABA triblock copolymer chain
## Abstract An electroactive triblock copolymer of poly(ethylene glycol) (PEG) and aniline pentamer (AP), PEG‐__block__‐AP‐__block__‐PEG (PAP), was synthesized via polycondensation in the presence of __N__,__N'__‐dicyclohexylcarbodiimide (DCC). The UV‐vis spectra and cyclic‐voltammograms (CV) spect
## Abstract The self‐assembly and photoresponsivity of amphiphilic azobenzene‐containing ABA triblock copolymers PA6C~__m__~‐__b__‐PEG~__n__~‐__b__‐PA6C~__m__~ synthesized by atom transfer radical polymerization (ATRP) were reported. Different self‐assembly morphologies formed by the gradual additi