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      Hyper-Cross-Linked Porous Polymer Featuring B–N Covalent Bonds (HCP-BNs): A Stable and Efficient Metal-Free Heterogeneous Photocatalyst

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          Abstract

          The first example of a porous polymer containing B–N covalent bonds, prepared from a tetraphene B–N monomer and biphenyl as a comonomer, is reported. It was prepared using the solvent knitting strategy, which allows the connection between the aromatic rings of the two monomers through methylene groups provided by an external cross-linking agent. The new polymer exhibited micromeso porosity with an S BET of 612 m 2/g, high thermal stability, and potential properties as a heterogeneous photocatalyst, since it is very active in the aza-Henry coupling reaction (>98% of conversion and selectivity). After the first run, the catalyst improves its photocatalytic activity, shortening the reaction time to only 2 h and maintaining this activity in successive runs. The presence of a radical in this structure that remains stable with successive runs makes it a new type of material with potential applications as a highly stable and efficient photocatalyst.

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          Most cited references30

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          Functional porous organic polymers for heterogeneous catalysis.

          Porous organic polymers (POPs), a class of highly crosslinked amorphous polymers possessing nano-pores, have recently emerged as a versatile platform for the deployment of catalysts. The bottom-up approach for porous organic polymer synthesis provides the opportunity for the design of polymer frameworks with various functionalities, for their use as catalysts or ligands. This tutorial review focuses on the framework structures and functionalities of catalytic POPs. Their structural design, functional framework synthesis and catalytic reactions are discussed along with some of the challenges.
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            A New Strategy to Microporous Polymers: Knitting Rigid Aromatic Building Blocks by External Cross-Linker

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              Porous organic polymers: a promising platform for efficient photocatalysis

              This review summarizes the latest advances of porous organic polymers (POPs) focusing on their applications in photocatalysis, including photocatalytic chemical transformations, photodetoxification of pollutants from water, and water splitting. Porous organic polymers (POPs) are a class of multi-dimensional porous network materials, which are built via strong covalent linkages between various organic building blocks with different geometries and topologies, and have recently become a rising research field in porous materials. POPs can be generally divided into two categories based on their degree of long-range order, including amorphous ( e.g. , CMPs, HCPs, PIMs, and PAFs) and crystalline ( e.g. , COFs). Owning to their advantages of light-weight, superior inherent porosity, excellent stability, pre-designable and tunable structures and functions, POPs have received increasing attention and research interest for their tremendous potential applications in gas storage/separation, heterogeneous catalysis, photoelectric conversion, chemical- and bio-sensing, energy storage and conversion, etc. Their porous structure, pore size, specific surface areas and functions can be directly designed and facilely tuned by introducing specific functional building blocks. In this review article, we summarize the latest representative advances in the field of POPs, focusing on their design and synthetic strategies, with emphasis on their specific applications in photocatalysis, including photocatalytic chemical transformation, photodetoxification of contaminants from water, and water splitting.
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                Author and article information

                Journal
                ACS Macro Lett
                ACS Macro Lett
                mz
                amlccd
                ACS Macro Letters
                American Chemical Society
                2161-1653
                29 June 2023
                18 July 2023
                : 12
                : 7
                : 949-954
                Affiliations
                []Department of Frontiers in Materials Chemistry, Instituto de Ciencia de Materiales de Madrid (ICMM-CSIC) , Sor Juana Inés de la Cruz, 3, Cantoblanco, Madrid 28049, Spain
                [§ ]Universidad de Alcalá (IRYCIS) , Departamento de Química Orgánica y Química Inorgánica, Instituto de Investigación Química “Andrés M. del Río” (IQAR), Campus Científico-Tecnológico, Facultad de Farmacia, Autovía A-II, Km 33.1, 28805-Alcalá de Henares, Madrid, Spain
                Author notes
                Author information
                https://orcid.org/0000-0002-2960-5404
                https://orcid.org/0000-0001-7373-4927
                https://orcid.org/0000-0002-0120-5599
                https://orcid.org/0000-0001-9522-0134
                Article
                10.1021/acsmacrolett.3c00217
                10357577
                37384421
                60005ecf-164c-41f5-8d8a-1b02dc26ef4c
                © 2023 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 10 April 2023
                : 13 June 2023
                Funding
                Funded by: Comunidad de Madrid, doi 10.13039/100012818;
                Award ID: 2018-T1/IND-10054
                Funded by: Universidad de Alcalá, doi 10.13039/501100006302;
                Award ID: PIUAH22/CC-016
                Funded by: Ministerio de Ciencia e Innovación, doi 10.13039/501100004837;
                Award ID: TED2021-129843B-I00
                Funded by: Ministerio de Ciencia e Innovación, doi 10.13039/501100004837;
                Award ID: PID2020-115128RB-I00
                Funded by: Ministerio de Ciencia e Innovación, doi 10.13039/501100004837;
                Award ID: PID2020-112590GB-C22
                Funded by: Consejo Superior de Investigaciones Científicas, doi 10.13039/501100003339;
                Award ID: NA
                Funded by: European Commission, doi 10.13039/501100000780;
                Award ID: NA
                Categories
                Letter
                Custom metadata
                mz3c00217
                mz3c00217

                Polymer chemistry
                Polymer chemistry

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