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Published on: April 22, 2016
Poly(arylene-ethynylene)s in Synthetic Heterogeneous Visible Light Photocatalysis: Structure-Reactivity Principles
Basile Weyl1, Benjamin Laroche1
1Molecular, Macromolecular Chemistry and Materials (C3M), ESPCI Paris PSL, UMR CNRS 7167, 10 rue Vauquelin, Paris 75005, (France).
Abstract:
Visible light photocatalysis has reshaped synthetic organic chemistry by enabling mild and selective radical processes. However, its widespread adoption is still constrained by the reliance on homogeneous photocatalysts, typically precious-metal complexes or organic dyes, which complicate recovery, recyclability, scalability, and integration into telescoped continuous flow processes. Heterogeneous photocatalysts (hPCs) offer a sustainable alternative, and among emerging candidates, π-conjugated polymers (π-CPs) have recently attracted attention as tunable, metal-free semiconductors capable of efficient visible light harvesting. This perspective highlights poly-(arylene-ethynylene)-s (PAEs), a distinctive subclass of π-CPs whose modular, conjugated backbones enable control over morphology, band structure, and excited-state behavior. Historically developed for optoelectronic applications, PAEs are now gaining traction as photocatalysts in synthetic organic chemistry, including in continuous flow reactors. Yet, the absence of systematic structure-reactivity relationships limits rational catalyst design and restricts broader deployment. Here, we examine emerging trends that link PAEs structure to photocatalytic function and articulate guiding principles for designing next-generation polymeric photocatalysts. By integrating concepts from materials science and synthetic methodology, this perspective aims to establish PAEs as robust, recyclable, and versatile platforms for sustainable photocatalysis.
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