000281716 001__ 281716 000281716 005__ 20240619091203.0 000281716 0247_ $$2doi$$a10.1021/acs.macromol.5b01316 000281716 0247_ $$2ISSN$$a0024-9297 000281716 0247_ $$2ISSN$$a1520-5835 000281716 0247_ $$2WOS$$aWOS:000361935600040 000281716 037__ $$aFZJ-2016-01404 000281716 041__ $$aEnglish 000281716 082__ $$a540 000281716 1001_ $$0P:(DE-HGF)0$$aGoracci, Guido$$b0$$eCorresponding author 000281716 245__ $$aInfluence of Solvent on Poly(2-(Dimethylamino)Ethyl Methacrylate) Dynamics in Polymer-Concentrated Mixtures: A Combined Neutron Scattering, Dielectric Spectroscopy, and Calorimetric Study 000281716 260__ $$aWashington, DC$$bSoc.$$c2015 000281716 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1454318121_19494 000281716 3367_ $$2DataCite$$aOutput Types/Journal article 000281716 3367_ $$00$$2EndNote$$aJournal Article 000281716 3367_ $$2BibTeX$$aARTICLE 000281716 3367_ $$2ORCID$$aJOURNAL_ARTICLE 000281716 3367_ $$2DRIVER$$aarticle 000281716 500__ $$a"final draft post referee" kann nicht beigebracht werden 000281716 520__ $$aWe have investigated the dynamical processes—α-relaxation, local motions of the side-groups, and methyl group rotations—in poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) in the dry state and in mixtures (at 70 wt% polymer concentration) with tetrahydrofuran (THF) and water, to address the question as to how these polymer motions are affected by plasticizers interacting in different ways with the polymer. Differential scanning calorimetry, dielectric spectroscopy, and neutron scattering techniques on labeled samples (with deuterated solvents to isolate the signal of the polymer component) have been combined. The α-relaxation is drastically affected, with similar shifts of the glass-transition temperature for both solvents. Effects of compositional heterogeneities and reduction of the fragility are also observed. On the contrary, methyl-group dynamics are unaffected by the presence of solvent. Regarding side-group local motions (β-relaxation), two kinds of components—a slow and a fast one—could be identified in the dry state. On the basis of the spatial information provided by neutron scattering, a model for the geometry of the motions involved in the fast component has been proposed. Adding solvent, this process would remain essentially unaltered, but the population involved in the slower one would be reduced. With THF as solvent, this reduction would be complete, but with water it would be only partial. This could be attributed to rather heterogeneous distribution of water molecules in the polymer likely associated with the presence of water clusters. 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