Noninvasive Substitution of K+ Sites in Cyclodextrin Metal–Organic Frameworks by Li+ Ions
Author(s) -
Hasmukh A. Patel,
Timur İslamoğlu,
Zhichang Liu,
Siva Krishna Mohan Nalluri,
Avik Samanta,
Ommid Anamimoghadam,
Christos D. Malliakas,
Omar K. Farha,
J. Fraser Stoddart
Publication year - 2017
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.7b06287
Subject(s) - chemistry , cyclodextrin , substitution (logic) , ion , metal ions in aqueous solution , metal , inorganic chemistry , radiochemistry , organic chemistry , computer science , programming language
Co-crystallization of K + and Li + ions with γ-cyclodextrin (γ-CD) has been shown to substitute the K + ion sites partially by Li + ions, while retaining the structural integrity and accessible porosity of CD-MOF-1 (MOF, metal-organic framework). A series of experiments, in which the K + /Li + ratio was varied with respect to that of γ-CD, have been conducted in order to achieve the highest possible proportion of Li + ions in the framework. Attempts to obtain a CD-MOF containing only Li + ions resulted in nonporous materials. The structural occupancy on the part of the Li + ions in the new CD-MOF has been confirmed by single-crystal X-ray analysis by determining the vacancies of K + -ion sites and accounting for the cation/γ-CD ratio in CD-MOF-1. The proportion of Li + ions has also been confirmed by elemental analysis, whereas powder X-ray diffraction has established the stability of the extended framework. This noninvasive synthetic approach to generating mixed-metal CD-MOFs is a promising method for obtaining porous framework unattainable de novo. Furthermore, the CO 2 and H 2 capture capacities of the Li + -ion-substituted CD-MOF have been shown to exceed the highest sorption capacities reported so far for CD-MOFs.
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