» Articles » PMID: 34465772

A Contorted Nanographene Shelter

Abstract

Nanographenes have kindled considerable interest in the fields of materials science and supramolecular chemistry as a result of their unique self-assembling and optoelectronic properties. Encapsulating the contorted nanographenes inside artificial receptors, however, remains challenging. Herein, we report the design and synthesis of a trigonal prismatic hexacationic cage, which has a large cavity and adopts a relatively flexible conformation. It serves as a receptor, not only for planar coronene, but also for contorted nanographene derivatives with diameters of approximately 15 Å and thicknesses of 7 Å. A comprehensive investigation of the host-guest interactions in the solid, solution and gaseous states by experimentation and theoretical calculations reveals collectively an induced-fit binding mechanism with high binding affinities between the cage and the nanographenes. Notably, the photostability of the nanographenes is improved significantly by the ultrafast deactivation of their excited states within the cage. Encapsulating the contorted nanographenes inside the cage provides a noncovalent strategy for regulating their photoreactivity.

Citing Articles

Chemically Mediated Artificial Electron Transport Chain.

Yang Y, Zhang Q, Khrouz L, Chau C, Yang J, Wang Y ACS Cent Sci. 2024; 10(6):1148-1155.

PMID: 38947209 PMC: 11212131. DOI: 10.1021/acscentsci.4c00165.


Tailored Water-Soluble Covalent Organic Cages for Encapsulation of Pyrene and Information Encryption.

Song H, Guo Y, Zhang G, Shi L Int J Mol Sci. 2023; 24(24).

PMID: 38139371 PMC: 10743434. DOI: 10.3390/ijms242417541.


Conformationally Confined Emissive Cationic Macrocycle with Photocontrolled Organelle-Specific Translocation.

Dong X, Dai X, Li G, Zhang Y, Xu X, Liu Y Adv Sci (Weinh). 2022; 9(23):e2201962.

PMID: 35713271 PMC: 9376817. DOI: 10.1002/advs.202201962.

References
1.
Wu J, Pisula W, Mullen K . Graphenes as potential material for electronics. Chem Rev. 2007; 107(3):718-47. DOI: 10.1021/cr068010r. View

2.
CRAM D . The design of molecular hosts, guests, and their complexes. Science. 1988; 240(4853):760-7. View

3.
Wu Y, Siegel J . Aromatic molecular-bowl hydrocarbons: synthetic derivatives, their structures, and physical properties. Chem Rev. 2006; 106(12):4843-67. DOI: 10.1021/cr050554q. View

4.
Peck E, Liu W, Spence G, Shaw S, Davis A, Destecroix H . Rapid Macrocycle Threading by a Fluorescent Dye-Polymer Conjugate in Water with Nanomolar Affinity. J Am Chem Soc. 2015; 137(27):8668-71. PMC: 4643739. DOI: 10.1021/jacs.5b03573. View

5.
Wang Y, Wu H, Li P, Chen S, Jones L, Mosquera M . Two-photon excited deep-red and near-infrared emissive organic co-crystals. Nat Commun. 2020; 11(1):4633. PMC: 7493989. DOI: 10.1038/s41467-020-18431-7. View