Add like
Add dislike
Add to saved papers

A series of sulfonic acid functionalized mixed-linker DUT-4 analogues: synthesis, gas sorption properties and catalytic performance.

In this work, we present the successful synthesis of a series of sulfonic acid functionalized mixed-linker metal-organic frameworks (MOFs) having the DUT-4 topology by using different ratios of 2,6-naphthalenedicarboxylic acid (H2 -NDC) and 4,8-disulfonaphthalene-2,6-dicarboxylic acid (H2 -NDC-2SO3 H) in one-pot reactions. The obtained materials were fully characterized and their CO2 adsorption properties at low and high pressures were studied and compared with those of the pristine DUT-4 material. Generally, the CO2 adsorption capacities range from 3.28 and 1.36 mmol g-1 for DUT-4 to 1.54 and 0.78 mmol g-1 for DUT-4-SO3 H (50) up to 1 bar at 273 K and 303 K, respectively. Computational calculations corroborated the structural changes of the material in function of the loading of sulfonic acid groups. Furthermore, due to the strong Brønsted acid character, the resulting sulfonic acid based MOF material was evaluated as a catalyst for the ring opening of styrene oxide with methanol as a nucleophile under mild conditions, showing almost full conversion (99%) after 5 hours of reaction. A hot filtration experiment demonstrated that the catalysis occurred heterogeneously and the catalyst could be recovered and reused for multiple runs without significant loss in activity and crystallinity.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app