作者: Hiroki KIMOTO , Atsuko FUKUDA , Atsushi ASANO , Takuzo KUROTSU
关键词: Polymer 、 Kinetic chain length 、 Chemistry 、 End-group 、 Methyl acrylate 、 Polymer chemistry 、 Side chain 、 Bulk polymerization 、 Physical chemistry 、 Polymerization 、 Living polymerization
摘要: The proton spin-spin relaxation time (T2) during the bulk polymerization of methyl acrylate was measured as a function reaction at various temperatures. Three kinds T2 (T2L (long), T2S (short) and T2M (intermediate)) were obtained proceeded. fraction (FS) increased sigmoidally certain time, while that T2L (FL) decreased reciprocally. former corresponded to amount polymer whose molecular weight sufficiently high enough cause tight entanglement produced transient network structure; latter reflected decrease in mixture monomer low polymer. is considered arise from relatively mobile region entanglement. relationship between fractions + yield found be linear, which led us monitor real non-distractive manner. 13C DD (dipolar decoupling)/MAS (magic angle spinning) NMR spectra also process terms motions main chain side formation structure. DD/MAS show motion became restricted well when “Trommosdorff effect” (gel effect) observed, part monomers trapped