Manzoor Faiza, Majeed Adnan, Ibrahim Ahmad H, Iqbal Muhammad Adnan, Rehman Asma, Aziz Sadia, Shahzadi Anam, Fatima Sabahat, Ejaz Sana, Zafar Muhammad Shehroz
Department of Chemistry, University of Agriculture Faisalabad Faisalabad 38040 Pakistan
Pharmacy Department, Faculty of Pharmacy, Tishk International University Erbil Iraq.
RSC Adv. 2025 Sep 12;15(40):33345-33364. doi: 10.1039/d5ra04650e. eCollection 2025 Sep 11.
Nickel (Ni)-catalyzed photoredox reactions are revolutionary methods that transform organic synthesis, enabling highly efficient and selective reactions under mild conditions. The synergy between Ni catalysis and photoredox catalysis is efficacious in activating inert bonds, creating potential reaction pathways, and accessing otherwise inaccessible molecular architectures. This review provides a detailed overview of advances in nickel/photoredox dual catalysis, with particular reference to insights into mechanisms and reaction scope. Among the key developments are enantioselective allyl carbamates, -phenethylamines, and aryl--nucleosides, as well as methods for hydroalkylation, aryl alkylation, and C-N/C-O coupling reactions. The single electron transfer (SET) processes and versatile oxidation states of Ni, coupled with organic and metal-based photocatalysts, underpin the dual catalytic cycles. Such innovations render Ni-catalyzed photoredox reactions more sustainable and cost-effective, providing a strong foundation for future advances in this area.
镍(Ni)催化的光氧化还原反应是变革有机合成的方法,能在温和条件下实现高效且选择性的反应。镍催化与光氧化还原催化之间的协同作用在活化惰性键、创造潜在反应途径以及构建难以通过其他方式获得的分子结构方面十分有效。本综述详细概述了镍/光氧化还原双催化的进展,特别提及了对反应机理和反应范围的见解。其中的关键进展包括对映选择性烯丙基氨基甲酸酯、苯乙胺和芳基核苷,以及氢烷基化、芳基烷基化和C-N/C-O偶联反应的方法。镍的单电子转移(SET)过程和多样的氧化态,与有机和金属基光催化剂相结合,构成了双催化循环的基础。这些创新使镍催化的光氧化还原反应更具可持续性和成本效益,为该领域未来的发展奠定了坚实基础。