Wang Danfeng, Malmberg Robert, Pernik Indrek, Prasad Shyamal K K, Roemer Max, Venkatesan Koushik, Schmidt Timothy W, Keaveney Sinead T, Messerle Barbara A
Department of Molecular Sciences , Macquarie University , North Ryde , NSW 2109 , Australia . Email:
ARC Centre of Excellence in Exciton Science , School of Chemistry , University of New South Wales , Kensington , NSW 2052 , Australia.
Chem Sci. 2020 Jun 5;11(24):6256-6267. doi: 10.1039/d0sc02703k. eCollection 2020 Jun 28.
While dual photocatalysis-transition metal catalysis strategies are extensively reported, the majority of systems feature two separate catalysts, limiting the potential for synergistic interactions between the catalytic centres. In this work we synthesised a series of tethered dual catalysts allowing us to investigate this underexplored area of dual catalysis. In particular, Ir(i) or Ir(iii) complexes were tethered to a BODIPY photocatalyst through different tethering modes. Extensive characterisation, including transient absorption spectroscopy, cyclic voltammetry and X-ray absorption spectroscopy, suggest that there are synergistic interactions between the catalysts. The tethered dual catalysts were more effective at promoting photocatalytic oxidation and Ir-catalysed dihydroalkoxylation, relative to the un-tethered species, highlighting that increases in both photocatalysis and Ir catalysis can be achieved. The potential of these catalysts was further demonstrated through novel sequential reactivity, and through switchable reactivity that is controlled by external stimuli (heat or light).
虽然双光催化-过渡金属催化策略已有广泛报道,但大多数体系都有两种单独的催化剂,这限制了催化中心之间协同相互作用的潜力。在这项工作中,我们合成了一系列 tethered 双催化剂,使我们能够研究这个尚未充分探索的双催化领域。特别是,Ir(i) 或 Ir(iii) 配合物通过不同的 tethering 模式连接到 BODIPY 光催化剂上。包括瞬态吸收光谱、循环伏安法和 X 射线吸收光谱在内的广泛表征表明,催化剂之间存在协同相互作用。相对于未连接的物种,tethered 双催化剂在促进光催化氧化和 Ir 催化的二氢烷氧基化方面更有效,这突出表明光催化和 Ir 催化都可以实现增强。这些催化剂的潜力通过新颖的顺序反应性以及由外部刺激(热或光)控制的可切换反应性得到了进一步证明。