Cation-induced chirality in a bifunctional metal-organic framework for quantitative enantioselective recognition View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2019-11-11

AUTHORS

Zongsu Han, Kunyu Wang, Yifan Guo, Wenjie Chen, Jiale Zhang, Xinran Zhang, Giuliano Siligardi, Sihai Yang, Zhen Zhou, Pingchuan Sun, Wei Shi, Peng Cheng

ABSTRACT

The integration of luminescence and chirality in easy-scalable metal-organic frameworks gives rise to the development of advanced luminescent sensors. To date, the synthesis of chiral metal-organic frameworks is poorly predictable and their chirality primarily originates from components that constitute the frameworks. By contrast, the introduction of chirality into the pores of metal-organic frameworks has not been explored to the best of our knowledge. Here, we demonstrate that chirality can be introduced into an anionic Zn-based metal-organic framework via simple cation exchange, yielding dual luminescent centers comprised of the ligand and Tb3+ ions, accompanied by a chiral center in the pores. This bifunctional material shows enantioselectivity luminescent sensing for a mixture of stereoisomers, demonstrated for Cinchonine and Cinchonidine epimers and amino alcohol enantiomers, from which the quantitative determination of the stereoisomeric excess has been obtained. This study paves a pathway for the design of multifunctional metal-organic framework systems as a useful method for rapid sensing of chiral molecules. More... »

PAGES

5117

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41467-019-13090-9

DOI

http://dx.doi.org/10.1038/s41467-019-13090-9

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1122475737

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/31712651


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