Highly Active La(III)-Based Metal-Organic Framework as a Heterogeneous Lewis Acid Catalyst for Friedel-Crafts Alkylation.

Chemistry

College of Chemistry and Materials Engineering, Wenzhou University, Chashan University Town, Wenzhou, Zhejiang Province, 325035, People's Republic of China.

Published: December 2022

AI Article Synopsis

  • - A new 2D metal-organic framework called SLX-2 was created from lanthanum and a specific tetracarboxylic acid, using a solvothermal method, and characterized using advanced techniques like X-ray diffraction.
  • - SLX-2 serves as a highly effective Lewis acid catalyst for alkylation reactions involving indole and pyrrole, achieving good yields and maintaining performance over 20 cycles with minimal loss in activity.
  • - This catalyst demonstrates exceptional stability in both acidic and basic conditions, outperforming previous catalysts in terms of durability while maintaining similar catalytic efficiency.

Article Abstract

In this study, a novel La(III)-based two-dimensional (2D) metal-organic framework, [La (qptca) ] (referred to as SLX-2), from LaCl and 1,1' : 4',1'' : 4'',1''' : 4''',1''''-quinquephenyl]-2,2'',2'''',5''-tetracarboxylic acid (H qptca) was synthesized by conventional solvothermal method and thoroughly characterized by using X-ray single-crystal diffraction, powder X-ray diffraction, and thermogravimetric analyses. The 2D SLX-2 features a unique lanthanum center exposed to the skeleton and was used as an efficient Lewis acid catalyst for the Friedel-Crafts alkylation of indole and pyrrole with β-nitrostyrene along with a wide substrate scope, giving the desired products in good-to-high yields under the optimal reaction conditions. Furthermore, the catalyst was used for twenty cycles, with nearly no effect on its activity, and the reaction was heterogeneous in nature. Moreover, compared to the previous hydrogen-bond-donating MOF catalysts for such alkylation reactions, SLX-2 showed an excellent stability toward harsh acidic and basic environment, and gave comparable catalytic activities.

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Source
http://dx.doi.org/10.1002/chem.202202441DOI Listing

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