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Abstract Photomediated Atom Transfer Radical Polymerization (photoATRP) is an activator regeneration method, which allows for the controlled synthesis of well‐defined polymers via light irradiation. Traditional photoATRP is often limited by the need for high‐energy ultraviolet or violet light. These could negatively affect the control and selectivity of the polymerization, promote side reactions, and may not be applicable to biologically relevant systems. This drawback can be circumvented by an introduction of the catalytic amount of photocatalysts, which absorb visible and/or NIR light and, therefore, controlled, regenerative ATRP can be performed with the dual‐catalytic cycle. Herein, a critical summary of recent developments in the field of dual‐catalysis concerning Cu‐catalyzed ATRP is provided. Contributions of involved species are examined mechanistically, followed by challenges and future directions towards the next generation of advanced functional macromolecular materials.
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Expanding the toolbox for development of metal‐based dual‐functional catalytic membranes
Abstract Catalytic membranes offer opportunities to develop modular, process‐intensified units. Dual‐functional materials, which integrate reactive and separation components in a single material, could play an important role in enabling them. Adapting the various characterization tools that are used to analyze the structures of metal‐based catalysts to these integrated structures could provide vital information for their design and implementation. In this perspective, we highlight the ways in which these tools can be used to analyze nonreactive membranes and non‐integrated systems where the catalyst and the membrane operate as two separate units. A methodology developed to analyze these comparatively simpler systems could be subsequently extended to integrated dual‐functional catalytic membranes. Thus, researchers from the catalysis and membranes communities can work together in a way that will not only lead to fundamental advancements in our understanding of catalytic membranes but also enable their transformation into real, scalable process‐intensified units.
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- Award ID(s):
- 2119688
- PAR ID:
- 10641454
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- AIChE Journal
- Volume:
- 69
- Issue:
- 11
- ISSN:
- 0001-1541
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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