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Updated: Feb 4, 2026

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
Published on: April 22, 2016
On Demand Switching of Polymerization Mechanism and Monomer Selectivity with Orthogonal Stimuli
Brian M Peterson1, Veronika Kottisch1, Michael J Supej1
1Cornell University, Ithaca, New York 14853, United States.
Abstract:
The development of next-generation materials is coupled with the ability to predictably and precisely synthesize polymers with well-defined structures and architectures. In this regard, the discovery of synthetic strategies that allow on demand control over monomer connectivity during polymerization would provide access to complex structures in a modular fashion and remains a grand challenge in polymer chemistry. In this Article, we report a method where monomer selectivity is controlled during the polymerization by the application of two orthogonal stimuli. Specifically, we developed a cationic polymerization where polymer chain growth is controlled by a chemical stimulus and paired it with a compatible photocontrolled radical polymerization. By alternating the application of the chemical and photochemical stimuli the incorporation of vinyl ethers and acrylates could be dictated by switching between cationic and radical polymerization mechanisms, respectively. This enables the synthesis of multiblock copolymers where each block length is governed by the amount of time a stimulus is applied, and the quantity of blocks is determined by the number of times the two stimuli are toggled. This new method allows on demand control over polymer structure with external influences and highlights the potential for using stimuli-controlled polymerizations to access novel materials.
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