ArticleSmall (Weinheim an der Bergstrasse, Germany)2026
Modular Donor-Acceptor Diradicaloids Based on an Electron Deficient N-Heteroacene Acceptor.
Article in Small (Weinheim an der Bergstrasse, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Conjugated organic molecules with open-shell diradical character (y) possess two weakly paired electron spins interacting across their constituent π-systems. These materials provide fundamental insight into the nature of electron pairing, enabling the utilization of the spin degree of freedom within emerging technologies. However, materials systems that synergistically offer high modularity, tunable y, high chemical stability, and interrelated (opto)electronic functionalities remain limited. Here, we report the facile synthesis of donor-acceptor-donor diradicaloids comprised of a central electron-deficient 6,7,8,9-tetrachloro-[1,2,5]thiadiazolo[3,4-b]phenazine acceptor flanked by electron-rich thiophene-based donors. Nuclear magnetic resonance and electron paramagnetic resonance spectroscopies, and theoretical investigations that account for the multiconfigurational nature of these species, connect a narrowing of the singlet-triplet splitting (∆E
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