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Dendronized Polymers with Ureidopyrimidinone Groups: An Efficient Strategy To Tailor Intermolecular Interactions, Rheology, and Fracture
Author(s) -
Leon F. Scherz,
Salvatore Costanzo,
Qian Huang,
A. Dieter Schlüter,
Dimitris Vlassopoulos
Publication year - 2017
Publication title -
macromolecules
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.994
H-Index - 313
eISSN - 1520-5835
pISSN - 0024-9297
DOI - 10.1021/acs.macromol.7b00747
Subject(s) - rheology , intermolecular force , viscoelasticity , polymer , materials science , polymer chemistry , shear thinning , hydrogen bond , polymerization , methacrylate , macromonomer , polymer science , composite material , chemistry , molecule , organic chemistry
A library of poly(methyl methacrylate)-based dendronized polymers with generation numbers g = 1–3 was prepared, which contain different degrees of dendritic substitution (0–50%) with strongly hydrogen bonding 2-ureido-4[1H]pyrimidinone (UPy) moieties at their respective g = 1 levels. Our rheological and thermal studies demonstrate that the strong intermolecular UPy interactions are suppressed for g = 2 and essentially eliminated for g = 3. Focusing on samples with short backbone degrees of polymerization (Pn ≈ 40), the linear viscoelastic response alters from liquid-like in the absence of UPy to gel-like with ever increasing moduli as the UPy content increases. Nonlinear rheological measurements indicate a transition from ductile to brittle behavior and, in parallel, a transition from shear strain thinning to shear strain hardening. This unique behavior makes UPy-DPs promising candidates for the design of new functional materials.

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