G-quadruplex organic frameworks

• Published in: Nature chemistry Vol. 9; no. 5; pp. 466 - 472
• Main Authors: 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., Wasielewski, Michael R.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.05.2017; Springer Nature; Nature Publishing Group
• Subjects: 119/118; 140/125; 639/638/440; 639/638/541; Analytical Chemistry; Biochemistry; Bioengineering; Chemistry; Chemistry, Multidisciplinary; Chemistry/Food Science; energy storage (including batteries and capacitors), charge transport, materials and chemistry by design, synthesis (novel materials); Hydrogen bonds; Inorganic Chemistry; Naphthalene; Organic Chemistry; Physical Chemistry; Physical Sciences; Science & Technology; United States > US; Colorado; Illinois; RECOMBINATION; DONOR; PHOTOINDUCED ELECTRON-TRANSFER; G-QUARTET; CHARGE-TRANSPORT; ENERGY-STORAGE; SEPARATION; POLARIZATION; BULK HETEROJUNCTION; HYDROGEN-BONDS
• ISSN: 1755-4330; 1755-4349
• DOI: 10.1038/nchem.2689

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. Using self-assembly to generate hydrogen-bonded organic networks is an underexplored method when preparing functional framework materials. Now, taking cue from DNA, bio-inspired G-quadruplexes are used as both intrinsic electron donors and hydrogen-bonding linkers to assemble rylene diimide acceptors. The resulting rectangular grids form layered crystalline frameworks, in which photoexcitation produces long-lived mobile charge carriers.