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G-quadruplex organic frameworks

Wu, Yi-Lin, Horwitz, Noah E., Chen, Kan-Sheng, Gomez-Gualdron, Diego A., Luu, Norman S., Ma, Lin, Wang, Timothy C., Hersam, Mark C., Hupp, Joseph T., Farha, Omar K., Snurr, Randall Q. and Wasielewski, Michael R. 2017. G-quadruplex organic frameworks. Nature Chemistry 9 , 466–472. 10.1038/nchem.2689

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Abstract

Two-dimensional covalent organic frameworks often π stack into crystalline solids that allow precise spatial positioning of molecular building blocks. Inspired by the hydrogen-bonded G-quadruplexes found frequently in guanine-rich DNA, here we show that this structural motif can be exploited to guide the self-assembly of naphthalene diimide and perylene diimide electron acceptors end-capped with two guanine electron donors into crystalline G-quadruplex-based organic frameworks, wherein the electron donors and acceptors form ordered, segregated π-stacked arrays. Time-resolved optical and electron paramagnetic resonance spectroscopies show that photogenerated holes and electrons in the frameworks have long lifetimes and display recombination kinetics typical of dissociated charge carriers. Moreover, the reduced acceptors form polarons in which the electron is shared over several molecules. The G-quadruplex frameworks also demonstrate potential as cathode materials in Li-ion batteries because of the favourable electron- and Li-ion-transporting capacity provided by the ordered rylene diimide arrays and G-quadruplex structures, respectively.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Chemistry
Publisher: Nature Publishing Group
ISSN: 1755-4330
Date of First Compliant Deposit: 16 January 2019
Date of Acceptance: 3 November 2016
Last Modified: 26 Nov 2020 14:59
URI: http://orca-mwe.cf.ac.uk/id/eprint/118421

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