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Qi Sun

Researcher at Zhejiang University

Publications -  160
Citations -  10951

Qi Sun is an academic researcher from Zhejiang University. The author has contributed to research in topics: Catalysis & Heterogeneous catalysis. The author has an hindex of 47, co-authored 146 publications receiving 7705 citations. Previous affiliations of Qi Sun include University of South Florida & Tianjin University.

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Postsynthetically Modified Covalent Organic Frameworks for Efficient and Effective Mercury Removal.

TL;DR: This work demonstrates how two-dimensional covalent organic frameworks (COFs) with well-defined mesopore structures display the right combination of properties to serve as a scaffold for decorating coordination sites to create ideal adsorbents in environmental remediation.
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Porous polymer catalysts with hierarchical structures

TL;DR: This tutorial review highlights the importance of the synthesis of hierarchically porous polymer based heterogeneous catalysts using sustainable routes under template-free and metal-free conditions.
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Covalent Organic Frameworks as a Decorating Platform for Utilization and Affinity Enhancement of Chelating Sites for Radionuclide Sequestration.

TL;DR: It is shown that 2D covalent organic frameworks (COFs) with unique structures possess all the traits to be well suited as a platform for the deployment of highly efficient sorbents such that they exhibit remarkable performance, as demonstrated by uranium capture.
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Transesterification Catalyzed by Ionic Liquids on Superhydrophobic Mesoporous Polymers: Heterogeneous Catalysts That Are Faster than Homogeneous Catalysts

TL;DR: It is demonstrated here that heterogeneous catalysts of ionic liquids functionalized on superhydrophobic mesoporous polymers exhibit much higher activities in transesterification to form biodiesel than homogeneous catalytic activities of the ionic liquid themselves.
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Flexibility Matters: Cooperative Active Sites in Covalent Organic Framework and Threaded Ionic Polymer

TL;DR: This work uncovers an entirely new strategy for designing bifunctional catalysts with double-activation behavior and opens a new avenue in the design of multicapable systems that mimic biocatalysis.