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Self‐assembly of telechelic polymers bearing adamantane groups via host‐guest inclusion complexes with cyclodextrin polymer
Author(s) -
Zhou Yingxue,
Yang Rongrong,
Fan Xiaodong,
Sun Mengmeng,
He Xinhai
Publication year - 2021
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.49520
Subject(s) - adamantane , polymer chemistry , micelle , acrylic acid , acrylate , polymerization , polymer , dynamic light scattering , copolymer , cyclodextrin , chain transfer , materials science , chemistry , radical polymerization , organic chemistry , nanoparticle , aqueous solution , nanotechnology
Self‐assembly and supramolecular inclusion complexations between telechelic polymers bearing one or double adamantane groups and linear poly(β‐cyclodextrin) (P(β‐CD)) were investigated in water. An adamantane (Ada) attached to poly (acrylic acid) (PAA) was prepared by reversible addition‐fragmentation chain transfer polymerization using s‐1‐dodecyl‐s″ ‐(α,α′‐dimethyl‐α″‐acetic acid) trithio‐carbonate functionalized Ada with tert‐butyl acrylate, followed by functional modification. Additionally, two Ada groups capped triblock copolymer F127 were obtained via an esterification reaction. The dynamic light scattering, transmission electron microscope and 1 H 2D NOSEY NMR spectroscopy were conducted to characterize the self‐assembly behaviors. With the inclusion complexation of Ada/CD in 1:1 M ratio in water, the spherical micelles were enlarged at 25°C than that of the adamantyl polymer precursors. Due to the PPO segment of Ada‐F127‐Ada, the micelles aggregation showed temperature dependence from 4 to 37°C for precursor and corresponding inclusion complexation; while in Ada‐PAA/P(β‐CD) system, the hydrodynamic diameters decreased with pH decreasing.