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Updated: Aug 11, 2025

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
Synthesis of High Molecular Weight Polymers by Organocatalyzed Living Radical Polymerization and Self-Assembly
Keling Hu1, Shun Liu1, Zhuo Zhao1
1State Key Laboratory of Separation Membranes and Membrane Processes, School of Chemistry, Tiangong University, Tianjin, 300387, P. R. China.
Abstract:
A mild organocatalyzed living radical polymerization method is studied for high molecular weight polymers (HMWPs), yielding low-dispersity linear and star polymers (Đ = Mw /Mn = 1.03-1.28) up to Mn = 3.9 × 105 and monomer conversion = 80%, where Mn and Mw are the number- and weight-average molecular weights, respectively. Even at high degrees of polymerization (DPs > 2000), this technique still features excellent control over molecular weights and Đ values, indicating the living character. The macroinitiators prepared at DP = 2000 are subsequently used for block polymerizations at high DPs (>2000) with functional methacrylates, yielding linear A-B diblock, linear B-A-B triblock, and 3-arm star A-B diblock copolymers, suggesting the excellent block efficiency of macroinitiators synthesized at a high DP value (=2000). This mild organocatalyzed living radical polymerization technique can enhance the livingness of propagation radicals and kinetic chain length at high monomer conversions for monomers with moderate propagation rate coefficients (kp s), reduce the persistent radical effect as much as possible, and hence enable HMWPs without the presence of metal catalyst, exogenous initiator, or harsh equipment. The obtained amphiphilic block copolymers present unique microphase separation behavior, and hold great potential in advanced materials applications, for example, thermosensitive nanocarriers.
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