Issue 24, 2021

Coordination-driven self-assembly of anthraquinone-based metal–organic cages for photocatalytic selective [2 + 2] cycloaddition

Abstract

Visible-light-promoted [2 + 2] cycloaddition provides a straightforward and efficient way to produce cyclobutanes, which are the core skeleton in commercial pharmaceuticals and fine chemicals. However, the control of the conformation to produce syn-head-to-head (syn-HH) cyclobutanes remains a grand challenge. In this work, we report the design and synthesis of anthraquinone-based metal–organic cages (MOCs) for the [2 + 2] photocycloaddition of chalcones to generate syn-HH cyclobutanes. Guided by the coordination-driven self-assembly strategy, one D2 and three D4h symmetric MOCs are constructed from anthraquinone-derived dicarboxylate linkers and 4-tert-butylsulfonylcalixarene capped tetrametallic clusters. The porous cages feature large hydrophobic cavities and photoactive anthraquinone units and are demonstrated to be efficient and recyclable photocatalysts for [2 + 2] cycloaddition of chalcones. The syn-HH diastereomers are obtained with up to 13 : 1 diastereomeric ratio (dr). The cage catalysts provide a well-defined confined space to accommodate the substrates, thus leading to enhanced selectivity relative to the free anthraquinone catalyst.

Graphical abstract: Coordination-driven self-assembly of anthraquinone-based metal–organic cages for photocatalytic selective [2 + 2] cycloaddition

Supplementary files

Article information

Article type
Paper
Submitted
26 Feb 2021
Accepted
26 Mey 2021
First published
27 Mey 2021

Dalton Trans., 2021,50, 8533-8539

Coordination-driven self-assembly of anthraquinone-based metal–organic cages for photocatalytic selective [2 + 2] cycloaddition

Y. Jin, H. Jiang, X. Tang, W. Zhang, Y. Liu and Y. Cui, Dalton Trans., 2021, 50, 8533 DOI: 10.1039/D1DT00652E

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