Abstract
We have developed a method to obtain a polymer gel consisting of a relatively homogeneous network structure composed of polymers with a narrow molecular weight simply by mixing the necessary compounds. In this method, a radical chain polymerization reaction with a fast reaction rate is combined with a radical addition cross-linking reaction that has a sufficiently slow reaction rate compared with the polymerization reaction. For the polymerization reaction, a multifunctional initiator with a strictly controlled number of polymerization initiation sites was used to prepare a star polymer with a chain number and length determined by living radical polymerization. In the cross-linking reaction, a multifunctional terminating agent was used to prepare a star polymer from a polymer with a narrow molecular weight via living radical polymerization followed by coupling with multiple polymer chains using a termination reaction. As a result, two kinds of reactions with greatly different kinetics occurred sequentially only when all of the compounds were mixed and allowed to stand at a constant temperature, and a relatively homogeneous network structure comprising cross-linked polymers with a low molecular weight distribution was inherently constructed.
Highlights
Polymer gels consist of a cross-linked three-dimensional polymer network swollen with excess solvent[1,2]
Using single-electron transfer living radical polymerization of a multifunctional initiator, namely, the four-branched halogenated organic compound pentaerythritol tetra(2-chloropropionate) (PETCP), enabled the synthesis of a star polymer composed of four monodisperse polymers
To investigate the influence of the solvent composition on the polymerization reaction, PETCP was employed as the initiator in a mixed solvent system of DMF/water at various compositions in which NIPA was used as the vinyl monomer to generate a thermoresponsive polymer
Summary
Polymer gels consist of a cross-linked three-dimensional polymer network swollen with excess solvent[1,2]. We elucidated a possible method of inherently constructing a polymer gel composed of a relatively homogeneous network structure in which various types of macromolecules of narrow molecular weight are cross-linked.
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