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Updated: Sep 22, 2025

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Orthogonal Modification of Polymers via Thio-Bromo "Click" Reaction and Supramolecular Chemistry: An Easy Method
Senbin Chen1, Dieter Ströhl2, Wolfgang H Binder1
1Chair of Macromolecular Chemistry, Faculty of Natural Science II (Chemistry, Physics and Mathematics), Martin-Luther University Halle-Wittenberg, Von-Danckelmann-Platz 4, Halle (Saale) D-06120, Germany.
Abstract:
Heterotelechelic poly(n-butyl acrylate)s (PnBuA) bearing two different and complementing supramolecular groups (namely, barbiturate (Ba) and the Hamilton wedge (HW)) at their α-end and ω-end (Ba-PnBuA-HW) were prepared by a combination of the reversible addition-fragmentation chain transfer (RAFT) process and the thio-bromo click reaction. The successful synthesis of the heterotelechelic H-bonding polymer Ba-PnBuA-HW (Mn,NMR = 7700 g/mol, Mn,SEC = 7500 g/mol, PDI = 1.25) was proven by a combination of 1H NMR and MALDI-TOF mass spectrometry. Self-assembly of the resulting heterotelechelic H-bonding polymers (Ba-PnBuA-HW) in a head-to-tail fashion driven by multiple H-bondings in solution and in the bulk was proven by temperature-dependent 1H NMR, concentration-dependent DOSY NMR studies, and rheological measurements.
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