Construction of Benzoxazine‐linked One‐Dimensional Covalent Organic Frameworks Using the Mannich Reaction

Author:

Cheng Cheng1ORCID,Liu Yikuan2,Sheng Guan2,Jiang Xinru2,Kang Xing1,Jiang Chao1,Liu Yan1,Zhu Yihan2,Cui Yong1ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules and State Key Laboratory of Metal Matrix Composites Shanghai Jiao Tong University Shanghai 200240 China

2. Center for Electron Microscopy, Institute for Frontier and Interdisciplinary Sciences, State Key Laboratory Breeding Base of Green Chemistry Synthesis Technology and College of Chemical Engineering Zhejiang University of Technology Hangzhou 310014, Zhejiang China

Abstract

AbstractCovalent polymerization of organic molecules into crystalline one‐dimensional (1D) polymers is effective for achieving desired thermal, optical, and electrical properties, yet it remains a persistent synthetic challenge for their inherent tendency to adopt amorphous or semicrystalline phases. Here we report a strategy to synthesize crystalline 1D covalent organic frameworks (COFs) composing quasi‐conjugated chains with benzoxazine linkages via the one‐pot Mannich reaction. Through [4+2] and [2+2] type Mannich condensation reactions, we fabricated stoichiometric and sub‐stoichiometric 1D covalent polymeric chains, respectively, using doubly and singly linked benzoxazine rings. The validity of their crystal structures has been directly visualized through state‐of‐the‐art cryogenic low‐dose electron microscopy techniques. Post‐synthetic functionalizations of them with a chiral MacMillan catalyst produce crystalline organic photocatalysts that demonstrated excellent catalytic and recyclable performance in light‐driven asymmetric alkylation of aldehydes, affording up to 94 % enantiomeric excess

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

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