Porous metal-organic alloys based on soluble coordination cages

Diverse strategies for the preparation of mixed-metal three-dimensional porous solids abound, although many of them lend themselves only moderate levels of tunability. Herein, we report the design and synthesis of surface functionalized permanently microporous coordination cages and their use in the...

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Published inChemical science (Cambridge) Vol. 11; no. 46; pp. 1254 - 12546
Main Authors Antonio, Alexandra M, Korman, Kyle J, Yap, Glenn P. A, Bloch, Eric D
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 07.12.2020
Royal Society of Chemistry (RSC)
The Royal Society of Chemistry
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Summary:Diverse strategies for the preparation of mixed-metal three-dimensional porous solids abound, although many of them lend themselves only moderate levels of tunability. Herein, we report the design and synthesis of surface functionalized permanently microporous coordination cages and their use in the isolation of mixed metal solids. Judicious alkoxide-based ligand functionalization was utilized to tune the solubility of starting copper( ii )-based cages and their resulting compatibility with the mixed-cage approach described here. We further prepared a family of isostructural molybdenum( ii ) cages for a subset of the ligands. The preparation of mixed-metal cage solids proceeds under facile conditions where solutions of parent cages are mixed and product phases isolated. A suite of spectroscopic and characterization tools confirm the starting cages are intact in the amorphous product. Finally, we show that utilization of precise ligand functional groups can be used to prepare mixed cage solids that can be easily and cleanly separated into their constituent components through simple solvent washing or solvent extraction techniques. Surface-functionalized porous coordination cages can be used to create homogeneous mixed-cage alloys with high levels of tunability and processability.
Bibliography:Electronic supplementary information (ESI) available. CCDC
For ESI and crystallographic data in CIF or other electronic format see DOI
2018425-2018427
10.1039/d0sc04941g
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
USDOE Office of Energy Efficiency and Renewable Energy (EERE)
EE0008813
These authors are joint first authors and contributed equally.
ISSN:2041-6520
2041-6539
DOI:10.1039/d0sc04941g