2026-05-28T16:42:52Zhttps://riuma.uma.es/rest/oai/request

oai:riuma.uma.es:10630/297972026-02-03T12:14:01Zcom_10630_2254col_10630_37959

A theoretical investigation of the diradical character and cyclophane formation in π-conjugated diradicals. Sánchez Rincón, Juan Badía-Domínguez, María Irene Ruiz-Delgado, María del Carmen Moléculas Ciclofanos Enlaces químicos π-Conjugated diradical compounds which feature unpaired electrons in the ground state are essential for understanding the nature of chemical bonds and have potential applications in material science1. In fact, an important research effort by our group has been directed towards carbazole-based diradicaloids2, aiming to explore how external stimuli impacts on supramolecular organization, and thus on the resulting optical and electronic properties. Thanks to this research, we have demonstrated that these materials are potential building blocks for dynamic covalent chemistry (DCC)3. In our present work, we wanted to explore beyond carbazole-based diradicals and analyse what would be the diradical character after modification of the chemical structure of the carbazole skeleton. For this purpose, we will analyse the structural and electronic properties of carbazole-based diradicals after the following chemical modifications: (i) heteroatom substitution, (ii) core elongation and (iii) insertion of donor/acceptor groups. In addition, the effect of the heteroatom substitution on the dynamic interconversion between the monomer and cyclophane aggregates will be also investigated. 2024-02-05T11:45:14Z 2024-02-05T11:45:14Z 2024-02-05T11:45:14Z 2024 conference output https://hdl.handle.net/10630/29797 eng 14th symposium on Conjugated pi-conjugated Compounds San Sebastian 08/02/2024 http://creativecommons.org/licenses/by-nc-nd/4.0/ open access Attribution-NonCommercial-NoDerivatives 4.0 Internacional