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Latest Advances in Highly Efficient Dye-Based Photoinitiating Systems for Radical Polymerization

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Light-activated polymerization is one of the most important and powerful strategies for fabrication of various types of advanced polymer materials. Because of many advantages, such as economy, efficiency, energy saving… Click to show full abstract

Light-activated polymerization is one of the most important and powerful strategies for fabrication of various types of advanced polymer materials. Because of many advantages, such as economy, efficiency, energy saving and being environmentally friendly, etc., photopolymerization is commonly used in different fields of science and technology. Generally, the initiation of polymerization reactions requires not only light energy but also the presence of a suitable photoinitiator (PI) in the photocurable composition. In recent years, dye-based photoinitiating systems have revolutionized and conquered the global market of innovative PIs. Since then, numerous photoinitiators for radical polymerization containing different organic dyes as light absorbers have been proposed. However, despite the large number of initiators designed, this topic is still relevant today. The interest towards dye-based photoinitiating systems continues to gain in importance, which is related to the need for new initiators capable of effectively initiating chain reactions under mild conditions. In this paper we present the most important information about photoinitiated radical polymerization. We describe the main directions for the application of this technique in various areas. Attention is mainly focused on the review of high-performance radical photoinitiators containing different sensitizers. Moreover, we present our latest achievements in the field of modern dye-based photoinitiating systems for the radical polymerization of acrylates.

Keywords: radical polymerization; based photoinitiating; dye based; systems radical; photoinitiating systems; polymerization

Journal Title: Polymers
Year Published: 2023

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