Development of Ni(II) Complexes Based on Thiosemicarbazides as Photocatalysts in Free-Radical Photopolymerization

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Palavras-chave:

nickel, thiosemicarbazides, photocatalyst, photopolymerization, LED

Resumo

Developing efficient and cost-effective photoinitiating systems that operate under mild conditions remains a key challenge in light-driven polymerization. In particular, the development of systems based on low-cost metal complexes has gained attention as a promising strategy to replace expensive transition metals such as ruthenium or iridium. In this context, monometallic Ni(II) complexes of the type [Ni(N,N,S-tsc)(4-aminopyridine)] (NiMe and NiPh), incorporating tridentate ligands derived from thiosemicarbazides, were synthesized. These complexes were characterized using various spectroscopic techniques, and their catalytic activity was evaluated in free-radical photopolymerization (FRP) reactions. This study investigates the role of light in modulating the reactivity of these nickel-based systems, aiming to elucidate their catalytic performance and contribute to the development of new transition-metal photocatalysts for applications in homogeneous catalysis.

Referências

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2. S. S. Tandon, M. C. Dul, J. L. Lee, L. N. Dawe, M. U. U. Anwar, L. K. Thompson, Dalton Transactions, 2011, 40, 3466-3475.

3. P. I. S. Maia, A. G. De A. Fernandes, N. J. J. N. Silva, A. D. Andricopulo, S. S. Lemos, E. S. Lang, U. Abram, V. M. Deflon, Journal of Inorganic Biochemistry, 2010, 104, 1276–1282.

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Publicado

03-11-2025

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Seção

Eletrocatálise e fotocatálise