From non-conductive MOF to proton-conducting metal-HOFs: a new class of reversible transformations induced by solvent-free mechanochemistry

Literature Information

Publication Date 2023-11-27
DOI 10.1039/D3SC04401G
Impact Factor 9.825
Authors

Marcin Oszajca, Dariusz Matoga


View Original

Abstract

Proton-conducting materials play an important role as solid electrolytes in electrochemical devices for energy storage and conversion, including proton exchange membrane fuel cells. Metal–organic frameworks (MOFs), covalent-organic frameworks (COFs) and more recently hydrogen-bonded organic frameworks (HOFs) have emerged as useful crystalline platforms for proton transport that provide high conductivity and enable insight into conduction pathways. Here, we present two new HOFs with high conductivity, reaching 2 × 10−2 S cm−1 at 60 °C and 75% relative humidity, obtained in reactions that represent a new class of reversible transformations of solids. The reactions are induced by solvent-free mechanochemistry and involve breaking of coordination linkages in a MOF and formation of extended hydrogen-bonded networks of metal-HOFs (MHOFs). This unprecedented class of MOF-to-MHOF transformations has been demonstrated using a non-conductive MOF (JUK-1) and formamidinium or methylammonium thiocyanates as solid reactants. Structural details of the solid-state reactions are revealed by powder X-ray diffraction and Rietveld refinements for the MHOF products. None of the attempts using conventional methods were successful in obtaining the MHOFs, emphasizing a unique role of mechanochemical stimuli in the reactivity of supramolecular polymer solids, including crystalline MOFs and HOFs. The reversible nature of non-covalent interactions in such materials may be utilized for the development of healable polymer systems.

Related Literature

Contents

Front/Back Matter

DOI: 10.1039/B814265N

Fabrication of mesoporous Pt nanotubes utilizing dual templates under a reduced pressure condition

Azusa Takai, Yusuke Yamauchi, Kazuyuki Kuroda

2008-05-08 Communication

DOI: 10.1039/B804072A

Controlled generation of acentric and homochiral coordination compounds from a versatile asymmetric ligand 4-(1H-1,2,4-triazol-3-yl)-4H-1,2,4-triazole

Jian Zhang, Zhao-Ji Li, Ye-Yan Qin, Jian-Kai Cheng, Yuan-Gen Yao

2008-07-15 Communication

DOI: 10.1039/B807320A

Biocompatible bacteria@Au composites for application in the photothermal destruction of cancer cells

Wen-Shuo Kuo, Ching-Ming Wu, Zih-Syuan Yang, Szu-Yu Chen, Cheng-Ying Chen, Chih-Chia Huang, Wei-Ming Li, Chi-Kuang Sun, Chen-Sheng Yeh

2008-08-20 Communication

DOI: 10.1039/B808871C

A simple route for fabricating poly(para-phenylene vinylene) (PPV) particles by using ionic liquids and a solvent evaporation process

Hiroshi Yabu, Atsunori Tajima, Takeshi Higuchi

2008-08-06 Communication

DOI: 10.1039/B809765H

Subtractive assembly of DNA nanoarchitectures driven by fuel strand displacement

Zhe Li, Yonggang Ke, Chenxiang Lin, Hao Yan, Yan Liu

2008-07-17 Communication

DOI: 10.1039/B807933A

Chemogenetic protein engineering: an efficient tool for the optimization of artificial metalloenzymes

Anca Pordea, Thomas R. Ward

2008-08-12 Feature Article

DOI: 10.1039/B806652C

Front cover

Cover

DOI: 10.1039/B814263G

You might also like

Compound Q&A

What precautions should be taken when handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3)?

When handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3), it ...

79206-94-34-(2-Furylmethyl)thi...
Compound Q&A

What precautions should be taken when handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9)?

When handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9), it...

71320-77-94-Chloro-N-[2-(4-mor...
Compound Q&A

How should waste containing 2-[2-(2-Methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate (CAS: 62921-74-8) be handled?

Waste containing this compound (CAS: 62921-74-8) should be handled according to ...

62921-74-82-[2-(2-Methoxyethox...
Compound Q&A

How should waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate be handled?

Waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate should be collected i...

40056-18-6(S)-Methyl 2-amino-3...
166882-70-85-({4-[(2S,4R)-4-Hyd...
Compound Q&A

Are there alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid (CAS: 7312-27-8) in synthesis?

There are several alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid in syn...

7312-27-8(2E)-3-(3,4-Dichloro...
Compound Q&A

How should Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84-9) be stored?

Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84...

925437-84-9Ethyl 6-(2-nitrophen...
Compound Q&A

How should waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) be handled?

Waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) should be coll...

18453-07-12-(1,3-Thiazol-2-yl)...
Compound Q&A

How is Methyl 5-iodo-2-methylbenzoate (CAS: 103440-54-6) typically synthesized?

Methyl 5-iodo-2-methylbenzoate can be synthesized through the iodination of meth...

103440-54-6Methyl 5-iodo-2-meth...
Compound Q&A

How is 5-Chloro[1,2,4]triazolo[1,5-a]pyridine (CAS: 1427399-34-5) typically synthesized?

5-Chloro[1,2,4]triazolo[1,5-a]pyridine is commonly synthesized via the condensat...

1427399-34-55-Chloro[1,2,4]triaz...

Source Journal

Chemical Science

Chemical Science
CiteScore: 14.4
Self-citation Rate: 3.9%
Articles per Year: 1413

Our journal has a wide-ranging scope which covers the full breadth of the chemical sciences. The research we publish contains the sorts of novel ideas, challenging questions and progressive thinking that bring undiscovered breakthroughs within reach. Your paper could focus on a single area, or cross many. It could be beyond the accepted bounds of the chemical sciences. It might address an immediate challenge, contribute to a future breakthrough or be wholly conceptual. We’re a team from every field of the chemical sciences, and know from experience that breakthroughs that drive the solutions to global challenges can come from anywhere, at any time. You could even start an entirely new area of research. Too bold? Too progressive? No such thing

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.