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Incorporation of Al 3+ Sites on Brønsted Acid Metal–Organic Frameworks for Glucose‐to‐Hydroxylmethylfurfural Transformation
Author(s) -
Tangsermvit Vitsarut,
Pila Taweesak,
Boekfa Bundet,
Somjit Vetiga,
Klysubun Wantana,
Limtrakul Jumras,
Horike Satoshi,
Kongpatpanich Kanokwan
Publication year - 2021
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.202006541
Subject(s) - lewis acids and bases , brønsted–lowry acid–base theory , catalysis , xanes , metal organic framework , chemistry , zirconium , density functional theory , yield (engineering) , metal , linker , materials science , inorganic chemistry , organic chemistry , computational chemistry , spectroscopy , physics , adsorption , quantum mechanics , metallurgy , computer science , operating system
5‐hydroxylmethylfurfural (HMF) is a bio‐based chemical that can be prepared from natural abundant glucose by using combined Brønsted–Lewis acid catalysts. In this work, Al 3+ catalytic site has been grafted on Brønsted metal–organic frameworks (MOFs) to enhance Brønsted–Lewis acidity of MOF catalysts for a one‐pot glucose‐to‐HMF transformation. The uniform porous structure of zirconium‐based MOFs allows the optimization of both acid strength and density of acid sites in MOF‐based catalysts by incorporating the desired amount of Al 3+ catalytic sites at the organic linker. Al 3+ sites generated via a post‐synthetic modification act as Lewis acid sites located adjacent to the Brønsted sulfonated sites of MOF structure. The local structure of the Al 3+ sites incorporated in MOFs has been elucidated by X‐ray absorption near‐edge structure (XANES) combined with density functional theory (DFT) calculations. The cooperative effect from Brønsted and Lewis acids located in close proximity and the high acid density is demonstrated as an important factor to achieve high yield of HMF.

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