Arkawazi, HDJ orcid.org/0000-0002-6973-6927, Clowes, R orcid.org/0009-0002-4686-2119, Cooper, AI orcid.org/0000-0003-0201-1021 et al. (4 more authors) (2019) Complex phase behaviour and structural transformations of metal-organic frameworks with mixed rigid and flexible bridging ligands. Chemistry - A European Journal, 25 (5). pp. 1353-1362. ISSN 0947-6539
Abstract
Two new heteroleptic metal-organic framework materials show strong adsorption of H2 and ethanol. [Co2(L1)(bdc)2], where L1 = N1,N4-bis(4-pyridinylmethyl)-2,5-dimethylbenzene-1,4-diamine and bdc is benzene-1,4-dicarboxylate, has a twofold interpenetrating pillared layer structure with pcu topology. It has a stepped, hysteretic EtOH adsorption that can be related to complicated phase and structural transformation behaviour that occurs on de-solvation and re-solvation, including major conformational changes to the geometry of the flexible L1 ligand. [Co2(L1)(bpdc)2], where bpdc = biphenyl-4,4’-dicarboxylate, has a unique six-connected self-catenating framework structure. Solvation changes occur without significant structural change and a partially-hydrolysed material binds its own decomposition products as guests.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2018 Wiley‐VCH Verlag GmbH & Co. This is an author produced version of a paper published in Chemistry - A European Journal. Uploaded in accordance with the publisher's self-archiving policy. |
Keywords: | Flexible structure; hydrogen storage; metal-organic framework; self-catenating; single-crystal-to-single-crystal |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemistry (Leeds) > Inorganic Chemistry (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 14 Nov 2018 15:58 |
Last Modified: | 17 Dec 2024 11:45 |
Status: | Published |
Publisher: | Wiley |
Identification Number: | 10.1002/chem.201805028 |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:138583 |