Sabri Zahra, Shadjou Nasrin, Mahmoudian Mehdi
Department of Nanotechnology, Faculty of Chemistry, Urmia University Urmia Iran
Institute of Nanotechnology, Urmia University Urmia Iran.
RSC Adv. 2024 Jan 15;14(4):2633-2651. doi: 10.1039/d3ra07629f. eCollection 2024 Jan 10.
Xanthene and acridine derivatives are interesting organic compounds that are used in different research fields like biomedicine and pharmaceutical science. However, applied catalysts for their synthesis have some limitations such as long reaction times, the need for harsh conditions and low yield. So, discovery of novel catalysts for the synthesis of xanthene and acridine derivatives is highly demanded. To overcome the limitation of previous methods on the efficient synthesis of 1,8-dioxo-octahydroxanthene and 1,8-dioxo-decahydroacridine derivatives, a green heterogeneous organic nano-catalyst (Cu@KCC-1-Pr-HMTA) was synthesized by covalent attachment of hexamethylenetetramine to the cavities and channels of dendritic mesoporous nanosilica (KCC-1). The prepared nano-catalyst was identified using various spectroscopic and microscopic methods including scanning electron microscopy (SEM), Fourier transform infrared (FT-IR), X-ray energy diffraction (EDX), EDX mapping and nitrogen adsorption-desorption analysis (BET-BJH). The prepared green nano-catalyst showed a spherical and dendritic structure with a surface area of 65.699 m g, average pore size of 40.78 nm and pore volume of 0.66 cm g. Also, Cu@KCC-1-Pr-HMTA has many chemo-active sites for the condensation reaction and was used as an efficient nano-catalyst towards one-step synthesis of 1,8-dioxo-decahydroacridine and 1,8-dioxo-octahydroxanthene derivatives from the reaction of aromatic aldehydes, dimedone, and ammonium acetate under solvent-free conditions. Short reaction times of 1 to 5 minutes for 1,8-dioxo-decahydroacridine and 30 to 55 minutes for 1,8-dioxo-octahydroxanthene derivatives, high yields and mild reaction conditions are advantages of the proposed synthetic method. It is hoped that the engineered nano-catalyst will be used for the synthesis of other organic compounds in the future.
呫吨和吖啶衍生物是有趣的有机化合物,用于生物医学和制药科学等不同研究领域。然而,用于其合成的催化剂存在一些局限性,如反应时间长、需要苛刻条件以及产率低。因此,迫切需要发现用于合成呫吨和吖啶衍生物的新型催化剂。为了克服先前方法在高效合成1,8 - 二氧代八氢呫吨和1,8 - 二氧代十氢吖啶衍生物方面的局限性,通过将六亚甲基四胺共价连接到树枝状介孔纳米二氧化硅(KCC - 1)的孔腔和通道中,合成了一种绿色多相有机纳米催化剂(Cu@KCC - 1 - Pr - HMTA)。使用包括扫描电子显微镜(SEM)、傅里叶变换红外光谱(FT - IR)、X射线能量衍射(EDX)、EDX映射和氮吸附 - 脱附分析(BET - BJH)等各种光谱和显微镜方法对制备的纳米催化剂进行了鉴定。制备的绿色纳米催化剂呈现出球形和树枝状结构,表面积为65.699 m²/g,平均孔径为40.78 nm,孔体积为0.66 cm³/g。此外,Cu@KCC - 1 - Pr - HMTA具有许多用于缩合反应的化学活性位点,并被用作一种高效的纳米催化剂,用于在无溶剂条件下由芳香醛、达米酮和醋酸铵反应一步合成1,8 - 二氧代十氢吖啶和1,8 - 二氧代八氢呫吨衍生物。1,8 - 二氧代十氢吖啶的反应时间为1至5分钟,1,8 - 二氧代八氢呫吨衍生物的反应时间为30至55分钟,反应时间短、产率高以及反应条件温和是所提出的合成方法的优点。希望这种工程化的纳米催化剂将来能用于合成其他有机化合物。