Publisher
Springer Science and Business Media LLC
Reference5 articles.
1. Kuang, H., Xu, C. & Tang, Z. Emerging chiral materials. Adv. Mater. 32, e2005110 (2020). A review article that presents developments and areas for future research in chiral materials.
2. Fernandez-Garcia, J. M., Izquierdo-Garcia, P., Buendía, M., Filippone, S. & Martín, N. Synthetic chiral molecular nanographenes: the key figure of the racemization barrier. Chem. Commun. 58, 2634–2645 (2022). A review article that describes common topological defects of nanographenes and techniques for determining their energy barriers and,therefore, relative configurational stability.
3. Izquierdo-García, P., Fernández-García, J. M., Perles, J., Fernández, I. & Martín, N. Electronic control of the Scholl reaction: selective synthesis of spiro vs helical nanographenes. Angew. Chem. Int. Ed. 61, e202215655 (2023). This paper describes that the Scholl reaction can be controlled through electronic effects of the starting substrates, affording different final products.
4. Ramírez-Barroso, S. et al. Curved nanographenes: multiple emission, thermally activated delayed fluorescence, and non-radiative decay. Adv. Mater. 35, e2212064 (2023). This paper reports results from the photophysical study of several molecular nanographenes using time-resolved and temperature-dependent photoluminescence spectroscopy.
5. Filippone, S., Maroto, E. E., Martín-Domenech, A., Suarez, M. & Martín, N. An efficient approach to chiral fullerene derivatives by catalytic enantioselective 1,3-dipolar cycloadditions. Nat. Chem. 1, 578–582 (2009). This paper reports the enantioselective catalytic synthesis of chiral fullerenes under mild conditions at low temperatures.