On the Mechanism Behind the Instability of Isoreticular Metal-Organic Frameworks (IRMOFs) in Humid Environments
Increasing the resistance to humid environments is mandatory for the implementation of isoreticular metal–organic frameworks (IRMOFs) in industry. To date, the causes behind the sensitivity of [Zn4(μ4‐O)(μ‐bdc)3]8 (IRMOF‐1; bdc=1,4‐benzenedicarboxylate) to water remain still open. A multiscale schem...
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Published in: | Chemistry : a European journal Vol. 18; no. 39; pp. 12260 - 12266 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Weinheim
WILEY-VCH Verlag
24-09-2012
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
Subjects: | |
Online Access: | Get full text |
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Summary: | Increasing the resistance to humid environments is mandatory for the implementation of isoreticular metal–organic frameworks (IRMOFs) in industry. To date, the causes behind the sensitivity of [Zn4(μ4‐O)(μ‐bdc)3]8 (IRMOF‐1; bdc=1,4‐benzenedicarboxylate) to water remain still open. A multiscale scheme that combines Monte Carlo simulations, density functional theory and first‐principles Born–Oppenheimer molecular dynamics on IRMOF‐1 was employed to unravel the underlying atomistic mechanism responsible for lattice disruption. At very low water contents, H2O molecules are isolated in the lattice but provoke a dynamic opening of the terephthalic acid, and the lattice collapse occurs at about 6 % water weight at room temperature. The ability of Zn to form fivefold coordination spheres and the increasing basicity of water when forming clusters are responsible for the displacement of the organic linker. The present results pave the way for synthetic challenges with new target linkers that might provide more robust IRMOF structures.
Troubled waters: The instability of an isoreticular metal–organic framework ([Zn4(μ4‐O)(μ‐bdc)3]8 (see figure); bdc=1,4‐benzenedicarboxylate) against moisture has been evaluated by means of a multiscale approach that indicates the role of water clusters in lattice disruption and the large contributions of configurational entropy. |
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Bibliography: | ark:/67375/WNG-Z5D5G20C-5 ERC-Starting Grant Bio2chem-d istex:1CFCEA42F9DD2E7B619F6E60C3900683D331F79F MICINN - No. CTQ2010-16077; No. CTQ2009-07753/BQU; No. CSD2006-0003; No. P07-FQM-02595 ArticleID:CHEM201201212 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201201212 |