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具有发光特性的β-酰基吡唑衍生物的环保合成方法。

Eco-friendly methods for the synthesis of -acyl pyrazole derivatives with luminescent properties.

作者信息

Świętczak Eliza, Rachwalski Michał, Pieczonka Adam Marek

机构信息

University of Lodz, Doctoral School of Exact and Natural Sciences Matejki 21/23 90-237 Lodz Poland.

University of Lodz, Faculty of Chemistry, Department of Organic and Applied Chemistry Tamka 12 PL-91-403 Lodz Poland

出版信息

RSC Adv. 2025 Apr 29;15(16):12698-12703. doi: 10.1039/d4ra08527b. eCollection 2025 Apr 16.

DOI:10.1039/d4ra08527b
PMID:40303902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12038390/
Abstract

A comparison of green methods for the synthesis of -acyl pyrazoles starting from aromatic carbohydrazide derivatives and 1,3-diketones is presented. Special attention was focused on reactions utilizing a ball mill enabling the synthesis of novel pyrazole derivatives with optimal yield and reproducibility. The use of this approach facilitated the synthesis of target compounds exhibiting solid-state luminescent properties attributable to the phenomenon of aggregation-induced emission (AIE). Additionally, efforts were made to prepare thin, luminescent solid-state films, allowing for the assessment of which synthesized compounds may have potential applications in organic electronics.

摘要

本文介绍了从芳香族酰肼衍生物和1,3 - 二酮开始合成α-酰基吡唑的绿色方法的比较。特别关注了利用球磨机的反应,该反应能够以最佳产率和可重复性合成新型吡唑衍生物。这种方法的使用促进了具有归因于聚集诱导发光(AIE)现象的固态发光特性的目标化合物的合成。此外,还努力制备薄的发光固态薄膜,以便评估哪些合成化合物可能在有机电子学中具有潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/12038390/1e3ffab6b57c/d4ra08527b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/12038390/ea327116c7c8/d4ra08527b-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/12038390/28948759cbcd/d4ra08527b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/12038390/1e3ffab6b57c/d4ra08527b-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/12038390/ea327116c7c8/d4ra08527b-s1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/12038390/28948759cbcd/d4ra08527b-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebc0/12038390/1e3ffab6b57c/d4ra08527b-f2.jpg

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本文引用的文献

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Azole reagents enabled ligation of peptide acyl pyrazoles for chemical protein synthesis.唑类试剂可实现肽酰吡唑的连接,用于化学蛋白质合成。
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Accessing N-Acyl Azoles via Oxoammonium Salt-Mediated Oxidative Amidation.通过氧铵盐介导的氧化酰胺化来获取 N-酰基唑。
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