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将镍(II)配合物固定在介孔改性KIT-6表面,作为一种新型、可重复使用且高效的纳米催化剂用于合成四唑和吡喃并吡唑衍生物。

Immobilization of Ni(ii) complex on the surface of mesoporous modified-KIT-6 as a new, reusable and highly efficient nanocatalyst for the synthesis of tetrazole and pyranopyrazole derivatives.

作者信息

Darabi Mitra, Nikoorazm Mohsen, Tahmasbi Bahman, Ghorbani-Choghamarani Arash

机构信息

Department of Chemistry, Faculty of Science, Ilam University P. O. Box 69315516 Ilam Iran

Department of Organic Chemistry, Faculty of Chemistry, Bu-Ali Sina University Hamedan 6517838683 Iran.

出版信息

RSC Adv. 2023 Apr 24;13(18):12572-12588. doi: 10.1039/d2ra08269a. eCollection 2023 Apr 17.

Abstract

In this paper, KIT-6@SMTU@Ni was successfully synthesized a new method of Ni(ii) complex stabilization on modified mesoporous KIT-6, as a novel and green heterogeneous catalyst. The obtained catalyst (KIT-6@SMTU@Ni) was characterized using Fourier transform infrared spectroscopy (FT-IR), Brunauer-Emmett-Teller (BET) calculation, X-ray diffraction (XRD), atomic absorption spectroscopy (AAS), energy-dispersive X-ray spectroscopy (EDS), X-ray mapping, thermogravimetric analysis (TGA) techniques and scanning electron microscopy (SEM). After complete characterization of the catalyst, it was successfully used for the synthesis of 5-substituted 1-tetrazoles and pyranopyrazoles. Moreover, tetrazoles were synthesized from benzonitrile derivatives and sodium azide (NaN). All tetrazole products were synthesized with high TON, TOF and excellent yields (88-98%) in a reasonable time (0.13-8 h), demonstrating the efficiency and practicality of the KIT-6@SMTU@Ni catalyst. Furthermore, pyranopyrazoles were prepared through the condensation reaction of benzaldehyde derivatives with malononitrile, hydrazine hydrate and ethyl acetoacetate with high TON, TOF and excellent yields (87-98%) at appropriate times (2-10.5 h). KIT-6@SMTU@Ni could be reused for five runs without any re-activation. Significantly, this plotted protocol has prominent benefits, such as applying green solvents, the use of commercially available and low-cost materials, excellent separation and reusability of the catalyst, short reaction time, high yield of products and a facile work-up.

摘要

在本文中,通过一种在改性介孔KIT-6上稳定镍(II)配合物的新方法,成功合成了KIT-6@SMTU@Ni,作为一种新型绿色多相催化剂。使用傅里叶变换红外光谱(FT-IR)、布鲁诺尔-埃米特-泰勒(BET)计算、X射线衍射(XRD)、原子吸收光谱(AAS)、能量色散X射线光谱(EDS)、X射线映射、热重分析(TGA)技术和扫描电子显微镜(SEM)对所得催化剂(KIT-6@SMTU@Ni)进行了表征。在对催化剂进行全面表征后,它成功用于合成5-取代-1-四唑和吡喃并吡唑。此外,四唑由苯甲腈衍生物和叠氮化钠(NaN)合成。所有四唑产物均在合理时间(0.13 - 8小时)内以高TON、TOF和优异产率(88 - 98%)合成,证明了KIT-6@SMTU@Ni催化剂的效率和实用性。此外,吡喃并吡唑是通过苯甲醛衍生物与丙二腈、水合肼和乙酰乙酸乙酯的缩合反应在适当时间(2 - 10.5小时)以高TON、TOF和优异产率(87 - 98%)制备的。KIT-6@SMTU@Ni可以重复使用五次而无需任何再活化。值得注意的是,该方案具有显著优点,如使用绿色溶剂、使用市售低成本材料、催化剂分离和可重复使用性优异、反应时间短、产物产率高以及后处理简便。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2b6/10123498/53f37bbfb1f5/d2ra08269a-s1.jpg

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