Visible Light-Driven C-3 Functionalization of Indoles over Conjugated Microporous Polymers
2018; American Chemical Society; Volume: 8; Issue: 9 Linguagem: Inglês
10.1021/acscatal.8b01478
ISSN2155-5435
AutoresWeijie Zhang, Juntao Tang, Wenguang Yu, Qing Huang, Yu Fu, Gui‐Chao Kuang, Chunyue Pan, Guipeng Yu,
Tópico(s)Metal-Organic Frameworks: Synthesis and Applications
ResumoMetal-free and heterogeneous organic photocatalysts provide an environmentally friendly alternative to traditional metal-based catalysts. This paper reports a series of carbazole-based conjugated microporous polymers (CMPs) with tunable redox potentials and explores their photocatalytic performance with regard to C-3 formylation and thiocyanation of indoles. Conjugated polymers were synthesized through FeCl3 mediated Friedel–Crafts reactions, and their redox potentials were well regulated by simply altering the nature of the core (i.e., 1,4-dibenzyl, 1,3,5-tribenzyl, or 1,3,5-triazin-2,4,6-triyl). The resulting CMPs exhibited high surface areas, visible light absorptions, and tunable semiconductor-range band gaps. With the highest oxidative capability, CMP-CSU6 derived from 1,3,5-tri(9H-carbazol-9-yl)benzene showed the highest efficiency for C-3 formylation and thiocyanation of indoles at room temperature. Notably, the as-made catalysts can be easily recovered with good retention of photocatalytic activity and reused at least five times, suggesting good recyclability. These results are significant for constructing high-performance porous polymer catalysts with tunable photoredox potentials targeting an efficient material design for catalysis.
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