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Polyglycidol Based Amphiphilic Double‐Comb Copolymers and Their Self‐Association in Aqueous Solution
Author(s) -
Ozdemir Firat,
Keul Helmut,
Mourran Ahmed,
Moeller Martin
Publication year - 2011
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/marc.201100175
Subject(s) - amphiphile , copolymer , monomer , polymer , polymer chemistry , side chain , aqueous solution , self assembly , materials science , polymersome , polymerization , bifunctional , chemical engineering , chemistry , organic chemistry , nanotechnology , catalysis , engineering , composite material
Herein, we report synthesis and self‐association properties of amphiphilic double‐comb polymers with polyglycidol backbones. First, a bifunctional polyglycidol precursor is synthesized via monomer activated anionic polymerization. Next, two efficient and orthogonal polymer analogous reactions are carried out for grafting hydrophilic oligoethylene glycol side chains and hydrophobic linear aliphatic side‐chains. The polymers are analyzed by means of NMR, GPC, and DSC. From the DSC analysis of the bulk samples it is evident that aliphatic side chains segregate from the polar backbone and thus crystallize. Furthermore, in aqueous media the double‐comb polymers spontaneously self‐assemble to form a multilayer structure. The present results pave a way to tailor and design amphiphilic polymers based on glycidols. Major advantages are spontaneous self‐assembly in water and the possibility to form onion polymersomes relevant to encapsulation.

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