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氢键有机骨架材料合成子的连续流合成进展

Progress in Continuous Flow Synthesis of Hydrogen-Bonded Organic Framework Material Synthons.

作者信息

Yao Xingjun, Wen Sanmiao, Ji Ningning, Deng Qiulin, Li Zhiliang, Wang Hongbing, Shang Qianqian

机构信息

Shandong Provincial Key Laboratory of Chemical Energy Storage and Novel Cell Technology, School of Chemistry and Chemical Engineering, Liaocheng University, Liaocheng 252059, China.

College of Chemistry and Chemical Engineering, Taishan University, Tai'an 271021, China.

出版信息

Molecules. 2024 Dec 26;30(1):41. doi: 10.3390/molecules30010041.

DOI:10.3390/molecules30010041
PMID:39795100
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11721421/
Abstract

Hydrogen-bonded organic framework (HOF) materials are typically formed by the self-assembly of small organic units (synthons) with specific functional groups through hydrogen bonding or other interactions. HOF is commonly used as an electrolyte for batteries. Well-designed HOF materials can enhance the proton exchange rate, thereby boosting battery performance. This paper reviews recent advancements in the continuous synthesis of HOF synthons, in the continuous synthesis of HOF's unit small molecules enabling the multi-step, rapid, and in situ synthesis of synthons, such as carboxylic acid, diaminotriazine (DAT), urea, guanidine, imidazole, pyrazole, pyridine, thiazole, triazole, and tetrazole, with online monitoring. Continuous flow reactors facilitate fast chemical reactions and precise microfluidic control, offering superior reaction speed, product yield, and selectivity compared to batch processes. Integrating the continuous synthesis of synthons with the construction of HOF materials on a single platform is essential for achieving low-cost, safe, and efficient processing, especially for reactions involving toxic, flammable, or explosive substances.

摘要

氢键有机框架(HOF)材料通常由带有特定官能团的小有机单元(合成子)通过氢键或其他相互作用自组装而成。HOF通常用作电池的电解质。精心设计的HOF材料可以提高质子交换速率,从而提升电池性能。本文综述了HOF合成子连续合成方面的最新进展,即在HOF单元小分子的连续合成中,实现诸如羧酸、二氨基三嗪(DAT)、尿素、胍、咪唑、吡唑、吡啶、噻唑、三唑和四唑等合成子的多步、快速和原位合成,并进行在线监测。连续流动反应器有助于快速化学反应和精确的微流体控制,与间歇过程相比,具有更高的反应速度、产物收率和选择性。将合成子的连续合成与在单一平台上构建HOF材料相结合,对于实现低成本、安全和高效的加工至关重要,特别是对于涉及有毒、易燃或易爆物质的反应。

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RSC Adv. 2024 Dec 2;14(51):38193-38199. doi: 10.1039/d4ra07120d. eCollection 2024 Nov 25.
2
An Update on the Nitrogen Heterocycle Compositions and Properties of U.S. FDA-Approved Pharmaceuticals (2013-2023).美国食品和药物管理局批准药物的含氮杂环组成和性质的最新进展(2013-2023 年)。
J Med Chem. 2024 Jul 25;67(14):11622-11655. doi: 10.1021/acs.jmedchem.4c01122. Epub 2024 Jul 12.
3
1,3,5-Triazine: Recent Development in Synthesis of its Analogs and Biological Profile.
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Mini Rev Med Chem. 2024;24(22):2019-2071. doi: 10.2174/0113895575309800240526180356.
4
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Nat Commun. 2024 May 10;15(1):3930. doi: 10.1038/s41467-024-48158-8.
5
Current Development of Thiazole-Containing Compounds as Potential Antibacterials against Methicillin-Resistant .含噻唑化合物作为抗耐甲氧西林菌潜在抗菌剂的当前进展
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6
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Pharmaceuticals (Basel). 2023 Feb 14;16(2):299. doi: 10.3390/ph16020299.
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9
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ACS Cent Sci. 2022 Dec 28;8(12):1589-1608. doi: 10.1021/acscentsci.2c01196. Epub 2022 Dec 16.
10
A practical flow synthesis of 1,2,3-triazoles.1,2,3-三唑的实用流动合成法。
RSC Adv. 2022 Oct 11;12(45):28910-28915. doi: 10.1039/d2ra04727f.