Gong Xiuyang, Gao Yang, Guo Yanxia, Cao Hongliang, Liu Jichang, Han Lu, Zhu Kake
State Key Laboratory of Green Chemical Engineering and Industrial Catalysis, East China University of Science and Technology, Shanghai, 200237, P.R. China.
School of Chemical Science and Engineering, Tongji University, Shanghai, 200092, P.R. China.
Chemistry. 2025 Jul 25;31(42):e202500969. doi: 10.1002/chem.202500969. Epub 2025 Jul 9.
Organic structure directing agents (OSDAs) based on asymmetric di-quaternary ammonia compounds have been rarely explored in crystallization of zeolites, owing to difficulties in structural control. Their use holds promise to regulate physicochemical properties of zeolitic materials toward enhancing the relevant catalytic performances. In this study, a stepwise alkylation of 1,4-diazabicyclo[2.2.2]octane (Dab) to generate asymmetric di-quaternary derivatives has been established, enabling their use as OSDAs in large pore zeolite synthesis. Through exploratory syntheses, we showed that small Me-Dab-Et can direct the formation of SBT zeolite in multiple inorganic cation (Cs─Na) crystallization, while the bulky Me-Dab-iPr and Me-Dab-sBu lead to the formation of FAU-SBT-SBS intergrowths. The obtained SBT zeolite exhibited higher olefin selectivity in catalytic upgrading of pyrolysis oil derived from polyethylene, with respect to alike cage-containing faujasite (FAU) zeolite. Our findings expand the library of asymmetric di-quaternary OSDAs and highlight their capability to achieve phase selective synthesis of large pore zeolites.
基于不对称二季铵化合物的有机结构导向剂(OSDAs)在沸石结晶中鲜有研究,因为其结构控制存在困难。它们的使用有望调节沸石材料的物理化学性质,从而提高相关的催化性能。在本研究中,已建立了1,4-二氮杂双环[2.2.2]辛烷(Dab)的逐步烷基化反应以生成不对称二季铵衍生物,使其能够用作大孔沸石合成中的OSDAs。通过探索性合成,我们发现小的Me-Dab-Et可以在多种无机阳离子(Cs─Na)结晶中指导SBT沸石的形成,而体积较大的Me-Dab-iPr和Me-Dab-sBu则导致FAU-SBT-SBS共生体的形成。相对于类似的含笼八面沸石(FAU)沸石,所获得的SBT沸石在聚乙烯衍生的热解油的催化提质中表现出更高的烯烃选择性。我们的研究结果扩展了不对称二季铵OSDAs的库,并突出了它们实现大孔沸石相选择性合成的能力。