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Post-Synthetically Elaborated BODIPY-Based Porous Organic Polymers (POPs) for the Photochemical Detoxification of a Sulfur Mustard Simulant

机译:基于后纯化的Bodipy的多孔有机聚合物(POPs)用于硫磺芥末模拟剂的光化学解毒

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摘要

Designing new materials for the effective detoxification of chemical warfare agents (CWAs) is of current interest given the recent use of CWAs. Although halogenated boron-dipyrromethene derivatives (4,4-difluoro-4-bora-3a,4a-diaza-s-in-dacene or BDP or BODIPY) at the 2 and 6 positions have been extensively explored as efficient photosensitizers for generating singlet oxygen (~1O_2) in homogeneous media, their utilization in the design of porous organic polymers (POPs) has remained elusive due to the difficulty of controlling polymerization processes through cross-coupling synthesis pathways. Our approach to overcome these difficulties and prepare halogenated BODIPY-based porous organic polymers (X-BDP-POP where X = Br or I) represents an attractive alternative through post-synthesis modification (PSM) of the parent hydrogenated polymer. Upon synthesis of both the parent polymer, H-BDP-POP, and its post-synthetically modified derivatives, Br-BDP-POP and I-BDP-POP, the BET surface areas of all POPs have been measured and found to be 640, 430, and 400 m~2·g~(-1), respectively. In addition, the insertion of heavy halogen atoms at the 2 and 6 positions of the BODIPY unit leads to the quenching of fluorescence (both polymer and solution-phase monomer forms) and the enhancement of phosphorescence (particularly for the iodo versions of the polymers and monomers), as a result of efficient intersystem crossing. The heterogeneous photocatalytic activities of both the parent POP and its derivatives for the detoxification of the sulfur mustard simulant, 2-chloroethyl ethyl sulfide (CEES), have been examined; the results show a significant enhancement in the generation of singlet oxygen (~1O_2). Both the bromination and iodination of H-BDP-POP served to shorten by 5-fold of the time needed for the selective and catalytic photo-oxidation of CEES to 2-chloroethyl ethyl sulfoxide (CEESO).
机译:为近期使用CWA的使用,设计用于化学疟原虫(CWA)的有效排毒的新材料是目前的利益。虽然2和6个位置的卤代硼 - 双甲基衍生物(4,4-二氟-4-硼-3a,4a-diaza-s-替代或BDP或BDP或BDP或BDP或BDPY)被广泛探索为有效的光敏剂,用于产生单线氧(〜1O_2)在均匀介质中,它们在多孔有机聚合物(POPs)设计中的利用由于通过交叉偶联合成途径控制聚合过程而难以捉摸。我们克服这些困难的方法并制备卤代的BODIPY基多孔有机聚合物(其中X = BR或I)代表母体氢化聚合物的合成后改性(PSM)的有吸引力的替代方案。在合成母体聚合物,H-BDP-POP和其合成后修饰的衍生物后,BR-BDP-POP和I-BDP-POP,已经测量了所有POP的BET表面区域,并发现为640, 430和400 m〜2·g〜(-1)。此外,在Bodipy单元的2和6位置插入重卤原子,导致荧光(聚合物和溶液相单体形式)的猝灭和磷光的增强(特别是聚合物的Iodo版本单体),由于有效的界面交叉。已经研究了母孔和其衍生物的异质光催化活性,用于硫磺芥末模拟剂,2-氯乙基硫醚(CEES)的解毒;结果表明,单次氧气(〜1O_2)的产生显着增强。 H-BDP-POP的溴化和碘化均用于缩短5倍的切片至2-氯乙基亚砜(CEESO)的选择性和催化光氧化所需的时间。

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  • 来源
    《Journal of the American Chemical Society》 |2020年第43期|18554-18564|共11页
  • 作者单位

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States Department of Bioinformatics and Genetics Faculty of Engineering and Natural Science Kadir Has University Istanbul Turkey;

    Department of Chemistry and Biochemistry Southern Illinois University Carbondale Illinois 62901 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

    Department of Chemistry and Biochemistry Southern Illinois University Carbondale Illinois 62901 United States;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States Institute of Molecular Design and Synthesis Tianjin University Nankai District Tianjin 300072 P. R. China School of Chemistry University of New South Wales Sydney NSW 2052 Australia;

    Department of Chemistry Northwestern University Evanston Illinois 60208-3113 United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 22:16:50

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