Single‐crystal‐to‐single‐crystal transformation of a two‐dimensional noninterpenetrated layer to a microporous three‐dimensional fourfold interpenetrated MOF triggered by DMF

We have demonstrated a single‐crystal‐to‐single‐crystal (SCSC) transformation from a two‐dimensional noninterpenetrated layer to a microporous three‐dimensional fourfold interpenetrated MOF. The centrosymmetric [Co2(μ2‐OH)(EIBA)3]n (SNUT‐25) transforms into a microporous [Co(EIBA)2]n (SNUT‐26), whic...

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Published in:Applied organometallic chemistry 2024-08, Vol.38 (8), p.n/a
Main Authors: Huang, Pei‐Pei, Wu, Ting‐Ting, Tuo, Meng‐Qi, Pan, Hui‐Bin, Yue, Si‐Yu, Huang, Pei, Gao, Yan‐Hong, Lu, Jiu‐Fu, Jin, Ling‐Xia
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Language:English
Subjects:
Benzoic acid
Chemical synthesis
crystal structure
Crystals
Dimensional changes
Dimethylformamide
electrocatalytic
Light irradiation
Metal-organic frameworks
Molecular structure
Nitric acid
Oxygen evolution reactions
photocatalytic activity
Photodegradation
solvothermal
syntheses
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creator Huang, Pei‐Pei
Wu, Ting‐Ting
Tuo, Meng‐Qi
Pan, Hui‐Bin
Yue, Si‐Yu
Huang, Pei
Gao, Yan‐Hong
Lu, Jiu‐Fu
Jin, Ling‐Xia
description We have demonstrated a single‐crystal‐to‐single‐crystal (SCSC) transformation from a two‐dimensional noninterpenetrated layer to a microporous three‐dimensional fourfold interpenetrated MOF. The centrosymmetric [Co2(μ2‐OH)(EIBA)3]n (SNUT‐25) transforms into a microporous [Co(EIBA)2]n (SNUT‐26), which is triggered by the reaction time with DMF that acts as a structure‐directing agent (HEIBA = 4‐(2‐ethyl‐1H‐imidazol‐1‐yl)benzoic acid; DMF = N,N′‐dimethylformamide). Despite the distinct structure and coordination arrangements of SNUT‐25 in contrast to SNUT‐26, both Co‐MOFs were synthesized using the same ligand. Fascinatingly, upon introducing a specific quantity of DMF combined with a negligible proportion of nitric acid, SNUT‐25 will progressively and completely transform into SNUT‐26. Under the synergistic induction of solvent molecules and temperature, SNUT‐25 changed from the original two‐dimensional layered structure to the three‐dimensional pore structure of SNUT‐26. In addition, SNUT‐25 and SNUT‐26 are efficient photocatalysts for the degradation of organic dye methyl blue (MB) under visible light irradiation. Surprisingly, the degradation rates of both SNUT‐25 and SNUT‐26 can reach over 96%. In addition, SNUT‐25 and SNUT‐26 also exhibited high electrocatalytic oxygen evolution reaction. We have successfully recorded the single crystal to single crystal (SCSC) transition from two‐dimensional non interpenetrating layers (SNUT‐25) to microporous three‐dimensional quadruple interpenetrating MOFs (SNUT‐26). Both SNUT‐25 and SNUT‐26 exhibit excellent electrocatalytic and photocatalytic performance.
doi_str_mv 10.1002/aoc.7590
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The centrosymmetric [Co2(μ2‐OH)(EIBA)3]n (SNUT‐25) transforms into a microporous [Co(EIBA)2]n (SNUT‐26), which is triggered by the reaction time with DMF that acts as a structure‐directing agent (HEIBA = 4‐(2‐ethyl‐1H‐imidazol‐1‐yl)benzoic acid; DMF = N,N′‐dimethylformamide). Despite the distinct structure and coordination arrangements of SNUT‐25 in contrast to SNUT‐26, both Co‐MOFs were synthesized using the same ligand. Fascinatingly, upon introducing a specific quantity of DMF combined with a negligible proportion of nitric acid, SNUT‐25 will progressively and completely transform into SNUT‐26. Under the synergistic induction of solvent molecules and temperature, SNUT‐25 changed from the original two‐dimensional layered structure to the three‐dimensional pore structure of SNUT‐26. In addition, SNUT‐25 and SNUT‐26 are efficient photocatalysts for the degradation of organic dye methyl blue (MB) under visible light irradiation. Surprisingly, the degradation rates of both SNUT‐25 and SNUT‐26 can reach over 96%. In addition, SNUT‐25 and SNUT‐26 also exhibited high electrocatalytic oxygen evolution reaction. We have successfully recorded the single crystal to single crystal (SCSC) transition from two‐dimensional non interpenetrating layers (SNUT‐25) to microporous three‐dimensional quadruple interpenetrating MOFs (SNUT‐26). 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The centrosymmetric [Co2(μ2‐OH)(EIBA)3]n (SNUT‐25) transforms into a microporous [Co(EIBA)2]n (SNUT‐26), which is triggered by the reaction time with DMF that acts as a structure‐directing agent (HEIBA = 4‐(2‐ethyl‐1H‐imidazol‐1‐yl)benzoic acid; DMF = N,N′‐dimethylformamide). Despite the distinct structure and coordination arrangements of SNUT‐25 in contrast to SNUT‐26, both Co‐MOFs were synthesized using the same ligand. Fascinatingly, upon introducing a specific quantity of DMF combined with a negligible proportion of nitric acid, SNUT‐25 will progressively and completely transform into SNUT‐26. Under the synergistic induction of solvent molecules and temperature, SNUT‐25 changed from the original two‐dimensional layered structure to the three‐dimensional pore structure of SNUT‐26. In addition, SNUT‐25 and SNUT‐26 are efficient photocatalysts for the degradation of organic dye methyl blue (MB) under visible light irradiation. Surprisingly, the degradation rates of both SNUT‐25 and SNUT‐26 can reach over 96%. In addition, SNUT‐25 and SNUT‐26 also exhibited high electrocatalytic oxygen evolution reaction. We have successfully recorded the single crystal to single crystal (SCSC) transition from two‐dimensional non interpenetrating layers (SNUT‐25) to microporous three‐dimensional quadruple interpenetrating MOFs (SNUT‐26). Both SNUT‐25 and SNUT‐26 exhibit excellent electrocatalytic and photocatalytic performance.</description><subject>Benzoic acid</subject><subject>Chemical synthesis</subject><subject>crystal structure</subject><subject>Crystals</subject><subject>Dimensional changes</subject><subject>Dimethylformamide</subject><subject>electrocatalytic</subject><subject>Light irradiation</subject><subject>Metal-organic frameworks</subject><subject>Molecular structure</subject><subject>Nitric acid</subject><subject>Oxygen evolution reactions</subject><subject>photocatalytic activity</subject><subject>Photodegradation</subject><subject>solvothermal</subject><subject>syntheses</subject><issn>0268-2605</issn><issn>1099-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1kUtOwzAQhi0EEqUgcQRLbNikjPOys6wKBaRWXQDryHXGJVUaB9sVyo4jcB6Ow0lwKatKbOalb0a__RNyyWDEAOIbadSIZwUckQGDooiAJ8UxGUCciyjOITslZ86tAaDIWTogX091u2rw--NT2d552YTKmxDcwZx6K1unjd1IX5uWGk0l9e87tKo32LowDFRr2rr1aDtsMWx4rGgje7TUm8BvamVNZ6zZOupfLeLBtjZbq01T0cMb88U0CKhXK7ShW_b0dj49JydaNg4v_vKQvEzvnicP0Wxx_zgZzyLFRAoRFgA8U0yrLOGgOWOJ0OFnBORpLBKsMhZqoRSwpax4kfAsLRguOY-FqgRLhuRqf7ez5m2LzpfrIDPIdWUCXIhU5GkWqOs9FV7onEVddrbeSNuXDMqdM2Vwptw5E9Boj77XDfb_cuV4MfnlfwCKu5mY</recordid><startdate>202408</startdate><enddate>202408</enddate><creator>Huang, Pei‐Pei</creator><creator>Wu, Ting‐Ting</creator><creator>Tuo, Meng‐Qi</creator><creator>Pan, Hui‐Bin</creator><creator>Yue, Si‐Yu</creator><creator>Huang, Pei</creator><creator>Gao, Yan‐Hong</creator><creator>Lu, Jiu‐Fu</creator><creator>Jin, Ling‐Xia</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0009-0003-3131-0562</orcidid><orcidid>https://orcid.org/0009-0005-4307-7459</orcidid><orcidid>https://orcid.org/0009-0004-8263-6295</orcidid><orcidid>https://orcid.org/0009-0002-7373-8391</orcidid><orcidid>https://orcid.org/0000-0003-2645-0512</orcidid><orcidid>https://orcid.org/0009-0007-5092-6935</orcidid><orcidid>https://orcid.org/0000-0001-7876-4674</orcidid><orcidid>https://orcid.org/0000-0001-7869-8021</orcidid><orcidid>https://orcid.org/0000-0002-2668-7475</orcidid></search><sort><creationdate>202408</creationdate><title>Single‐crystal‐to‐single‐crystal transformation of a two‐dimensional noninterpenetrated layer to a microporous three‐dimensional fourfold interpenetrated MOF triggered by DMF</title><author>Huang, Pei‐Pei ; 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The centrosymmetric [Co2(μ2‐OH)(EIBA)3]n (SNUT‐25) transforms into a microporous [Co(EIBA)2]n (SNUT‐26), which is triggered by the reaction time with DMF that acts as a structure‐directing agent (HEIBA = 4‐(2‐ethyl‐1H‐imidazol‐1‐yl)benzoic acid; DMF = N,N′‐dimethylformamide). Despite the distinct structure and coordination arrangements of SNUT‐25 in contrast to SNUT‐26, both Co‐MOFs were synthesized using the same ligand. Fascinatingly, upon introducing a specific quantity of DMF combined with a negligible proportion of nitric acid, SNUT‐25 will progressively and completely transform into SNUT‐26. Under the synergistic induction of solvent molecules and temperature, SNUT‐25 changed from the original two‐dimensional layered structure to the three‐dimensional pore structure of SNUT‐26. In addition, SNUT‐25 and SNUT‐26 are efficient photocatalysts for the degradation of organic dye methyl blue (MB) under visible light irradiation. Surprisingly, the degradation rates of both SNUT‐25 and SNUT‐26 can reach over 96%. In addition, SNUT‐25 and SNUT‐26 also exhibited high electrocatalytic oxygen evolution reaction. We have successfully recorded the single crystal to single crystal (SCSC) transition from two‐dimensional non interpenetrating layers (SNUT‐25) to microporous three‐dimensional quadruple interpenetrating MOFs (SNUT‐26). 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subjects Benzoic acid
Chemical synthesis
crystal structure
Crystals
Dimensional changes
Dimethylformamide
electrocatalytic
Light irradiation
Metal-organic frameworks
Molecular structure
Nitric acid
Oxygen evolution reactions
photocatalytic activity
Photodegradation
solvothermal
syntheses
title Single‐crystal‐to‐single‐crystal transformation of a two‐dimensional noninterpenetrated layer to a microporous three‐dimensional fourfold interpenetrated MOF triggered by DMF
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