Molecular characterization of soluble poly(1,4‐divinylbenzene) obtained by anionic polymerization of 1,4‐divinylbenzene with lithium alkylamide as initiator
Kanji Kajiwara, Hidematsu Suzuki, Hiroshi Inagaki, Mizuo Maeda, Teiji Tsuruta
Abstract
Kanji Kajiwara, Hidematsu Suzuki, Hiroshi Inagaki, Mizuo Maeda, Teiji Tsuruta
Abstract
Abstract A series of soluble poly(1,4‐divinylbenzene) (PDVB) samples was prepared by anionic polymerization of 1,4‐divinylbenzene (DVB) in tetrahydrofuran with a varying amount of diisopropylamine. The dilute solution properties of the PDVB samples were examined with conventional methods including viscosimetry, sedimentation equilibrium, and light scattering measurements. The results suggest a considerable amount of long branches in soluble PDVB though not all of the pendant vinyl groups are consumed to form branches. A tree‐like model was proposed for the present system. The data were analysed quantitatively according to this model which yielded a consistent pair of values of the z‐average mean‐square radius of gyration 〈S2〉 and the intrinsic viscosity [η].
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Abstract A series of soluble poly(1,4‐divinylbenzene) (PDVB) samples was prepared by anionic polymerization of 1,4‐divinylbenzene (DVB) in tetrahydrofuran with a varying amount of diisopropylamine. The dilute solution properties of the PDVB samples were examined with conventional methods including viscosimetry, sedimentation equilibrium, and light scattering measurements. The results suggest a considerable amount of long branches in soluble PDVB though not all of the pendant vinyl groups are consumed to form branches. A tree‐like model was proposed for the present system. The data were analysed quantitatively according to this model which yielded a consistent pair of values of the z‐average mean‐square radius of gyration 〈S2〉 and the intrinsic viscosity [η].
Key concepts: Divinylbenzene, Anionic addition polymerization, Chemistry, Polymerization, Polymer chemistry, Tetrahydrofuran, Lithium (medication), Radius of gyration