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Article Abstract

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.

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http://dx.doi.org/10.1002/chem.202500969DOI Listing

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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.

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Non-Equilibrium Kinetic States of a [2]Rotaxane-Based Molecular Shuttle Controlled by Acid Concentrations.

Angew Chem Int Ed Engl

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Shenzhen Grubbs Institute, Guangdong Provincial Key Laboratory of Catalysis, and Department of Chemistry, Southern University of Science and Technology (SUSTech), Xueyuan Blvd 1088, Shenzhen, 518055, China.

A [2]rotaxane-based molecular shuttle with an acid-responsive asymmetric macrocycle on a symmetric dumbbell axle is reported. Upon adding TFA, the macrocycle, namely the amine naphthotube, is protonated and translocates from the di(quaternary ammonium) station to the triazole stations because of electrostatic repulsion and weakened binding. The shuttling kinetics are slow due to the steric hindrance caused by the ethyl group on the quaternary ammonium center and can be followed by H NMR spectroscopy.

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