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磺酸官能化多孔有机聚合物作为一种非均相催化剂用于高效假四组分合成二氢-2-氧代吡咯。

Sulfonic acid functionalized porous organic polymer as a heterogeneous catalyst for efficient pseudo four-component synthesis of dihydro-2-oxypyrroles.

作者信息

Daliran Saba, Hosseini Seyedeh Fatemeh, Oveisi Ali Reza, Sanchooli Esmael, Rodríguez-Castellón Enrique, Ballesteros-Plata Daniel

机构信息

Department of Organic Chemistry, Faculty of Chemistry, Lorestan University, Khorramabad, 68151-44316, Iran.

Department of Chemistry, University of Zabol, P.O. Box: 98615-538, Zabol, Iran.

出版信息

BMC Chem. 2025 Jul 17;19(1):215. doi: 10.1186/s13065-025-01583-2.

DOI:10.1186/s13065-025-01583-2
PMID:40676673
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12273233/
Abstract

BACKGROUND

A new sulfonated porous organic polymer (POP-SOH) is synthesized through post-synthetic modification of (PSM) of the COF-366 through a two-step process: first, transformation of imine (C = N) functional groups into amine (C-N) linkages, followed by treatment of the amine groups with 1,3-propane sultone. Then, it was used for the first time as an efficient heterogeneous catalyst for the preparation of dihydro-2-oxo pyrroles under mild conditions.

RESULTS

The nominal solid was characterized and confirmed by a variety of techniques such as FT-IR, PXRD, SEM/EDX, UV-Vis DRS, XPS, HRTEM, BET surface area and TGA/DSC. The catalytic performance of POP-SOH was assessed and optimized in the pseudo four-component synthesis of dihydro-2-oxopyrroles. Accordingly, the optimal conditions were found to be 20 mg of POP-SOH in methanol at room temperature for 1 h, giving the highest product yield of 92% of the desired product.

CONCLUSION

The above procedure demonstrated remarkable advantages such as high product yields, operational simplicity, short reaction times, and excellent catalyst reusability (four consecutive cycles without significant loss of activity). The catalyst showed superior performance compared to the pristine COF and many existing systems, operating efficiently at room temperature with a relatively low catalyst loading.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1186/s13065-025-01583-2.

摘要

背景

通过两步法对COF-366进行后合成修饰(PSM)合成了一种新型磺化多孔有机聚合物(POP-SOH):首先,将亚胺(C=N)官能团转化为胺(C-N)键,然后用1,3-丙烷磺酸内酯处理胺基。然后,它首次被用作在温和条件下制备二氢-2-氧代吡咯的高效多相催化剂。

结果

通过多种技术对该标称固体进行了表征和确认,如傅里叶变换红外光谱(FT-IR)、粉末X射线衍射(PXRD)、扫描电子显微镜/能谱仪(SEM/EDX)、紫外可见漫反射光谱(UV-Vis DRS)、X射线光电子能谱(XPS)、高分辨率透射电子显微镜(HRTEM)、比表面积(BET)和热重分析/差示扫描量热法(TGA/DSC)。在二氢-2-氧代吡咯的准四组分合成中评估并优化了POP-SOH的催化性能。因此,发现最佳条件是在室温下于甲醇中使用20 mg POP-SOH反应1小时,所需产物的最高产率为92%。

结论

上述方法显示出显著优势,如高产率、操作简单、反应时间短和优异的催化剂可重复使用性(连续四个循环且活性无明显损失)。与原始COF和许多现有体系相比,该催化剂表现出优异的性能,在室温下以相对较低的催化剂负载量高效运行。

补充信息

在线版本包含可在10.1186/s13065-025-01583-2获取的补充材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/d8e06f408a3c/13065_2025_1583_Sch3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/4d96b6b432b8/13065_2025_1583_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/bf68b5c5938c/13065_2025_1583_Sch2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/77ab1e3b4550/13065_2025_1583_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/1bdcb330561f/13065_2025_1583_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/ef253a827104/13065_2025_1583_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/d9075d028741/13065_2025_1583_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/3cbf5029943d/13065_2025_1583_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/1db0f73b0fbd/13065_2025_1583_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/d8e06f408a3c/13065_2025_1583_Sch3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/4d96b6b432b8/13065_2025_1583_Sch1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/bf68b5c5938c/13065_2025_1583_Sch2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/77ab1e3b4550/13065_2025_1583_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/1bdcb330561f/13065_2025_1583_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/ef253a827104/13065_2025_1583_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/d9075d028741/13065_2025_1583_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/3cbf5029943d/13065_2025_1583_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/1db0f73b0fbd/13065_2025_1583_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68cf/12273233/d8e06f408a3c/13065_2025_1583_Sch3_HTML.jpg

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