4.8 Article

Dual-catalyst engineered porous organic framework for visible-light triggered, metal-free and aerobic sp3 C-H activation in highly synergistic and recyclable fashion

Journal

JOURNAL OF CATALYSIS
Volume 394, Issue -, Pages 40-49

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcat.2020.12.013

Keywords

Porous organic framework; Dual-catalyst engineering; Photo-organo catalysis; Atom-economy; Metal-free reaction; C-H activation

Funding

  1. CSIR [MLP-0028]
  2. CSIR, New Delhi, India

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By combining photoredox and organo-catalysis methods, a new approach for constructing carbon-carbon bonds on a two-dimensional porous organic framework has been developed. The catalyst, using oxygen as the oxidant and visible light as the trigger, can successfully synthesize biorelevant products at room temperature, showing excellent reusability and economic viability.
Photoredox and organo-catalysis denote powerful construction tools for new classes of carbon-carbon bonds, where incisive amalgamation of both the approaches over a single, recyclable platform can bring about synergic and eco-friendly reactions under mild conditions. Aiming at enamine-based photoredox catalysis for atom-economic and metal-free sp(3 )C-H activation, an amide-based two-dimensional (2D) porous organic framework (POF) is devised. The pendent -NH2 groups are judiciously anchored with two catalytic stations viz. Rose Bengal and L-proline, through stepwise variation of solid phase peptide synthesis. The dual-catalyst engineered POF represents a fully organic material that synergistically performs visible-light triggered oxidative Mannich reaction to produce biorelevant heterocycle beta-amino ketone in excellent yield at room temperature, using oxygen as clean and selective oxidant. Importantly, activity of this bi-functionalized catalyst compares favorably well to individual homogeneous counterparts. The covalently modified framework demonstrates economic viability via gram-scale synthesis besides admirable reusability, and proves to be effective for nineteen varieties of substrates. The photocatalytic path is detailed from efficient energy transfer from host polymer to substrate in light of experimental and theoretical studies, which provides proof-of-concept to the photo-organo combined mechanism. The material benefits heterogenising two homogeneous catalysts, besides excluding additional steps of conventional Mannich reactions, and offers a step-forward to smart and green cross-dehydrogenative coupling reactions. (C) 2020 Elsevier Inc. All rights reserved.

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