Metal‐Carboxyl Helical Chain Secondary Units Supported Ion‐Exchangeable Anionic Uranyl–Organic Framework
As a less explored avenue, actinide‐based metal‐organic frameworks (MOFs) are worth studying for the particularity of actinide nodes in coordination behaviour and assembly modes. In this work, an azobenzenetetracarboxylate‐based anionic MOF supported by uranyl–carboxyl helical chain units was synthe...
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Published in | Chemistry : a European journal Vol. 25; no. 44; pp. 10309 - 10313 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
06.08.2019
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Subjects | |
Online Access | Get full text |
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Summary: | As a less explored avenue, actinide‐based metal‐organic frameworks (MOFs) are worth studying for the particularity of actinide nodes in coordination behaviour and assembly modes. In this work, an azobenzenetetracarboxylate‐based anionic MOF supported by uranyl–carboxyl helical chain units was synthesized, incorporating linear uranyl as the metal centre. This kind of helical chain‐type building unit is reported for the first time in uranyl‐based MOFs. Structural analysis reveals that the formation of helical chain secondary units can be attributed to restricted equatorial coordination of rigid flat azobenzene ligand to uranyl centres. Meanwhile, this newly‐synthesized anionic material has been used to remove Eu3+ ions, as a non‐radioactive surrogate of Am3+ ion, through an ion‐exchange process with [(CH3)2NH2]+ ions in its open channels, as evidenced by a combination of 1H NMR spectroscopy, EDS and PXRD.
Chain gang: An anionic uranyl–organic framework supported by metal‐carboxyl helical chain units can selectively remove Eu3+ ion, a non‐radioactive surrogate of Am3+ ion, through ion‐exchange with [(CH3)2NH2]+ ions in its open channels. |
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Bibliography: | These authors contributed equally to this work. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0947-6539 1521-3765 1521-3765 |
DOI: | 10.1002/chem.201902180 |