Rapid One‐Step Synthesis of Complex‐Architecture Block Polymers Using Inductively “Armed–Disarmed” Monomer Pairs

Boyce S. Chang; Stephanie Oyola‐Reynoso; Joel Cutinho; Martin M. Thuo

Index: 10.1002/marc.201800026

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Abstract

A facile method is reported for rapid, room‐temperature synthesis of block copolymers (BCP) of complex morphology and hence nontraditional spherical assembly. The use of solvated electrons generates radical anions on olefinic monomers, and with a felicitous choice of monomer pairs, this species will propagate bimechanistically (via radical and the anion) to form BCPs. Molecular weight of the obtained BCP range from Mw = 97 000–404 000 g mol−1 (polydispersity index, PDI = 1.4–3.0) depending on monomer pairs. The composition of the blocks can be controlled by changing monomer ratio, with the caveat that yield is affected. Detailed characterization by 2D nuclear magnetic resonance spectroscopy, differential scanning calorimetry (DSC), and analysis of the mechanisms involved indicate the structure of obtained block copolymers to be at least a triblock with a complex central unit. Evaluating trends in the Hammett parameter segregates monomer pairs into “armed and disarmed” groups with respect to radical or anionic polymerization akin to oligosaccharides synthesis.