Singlet fission (SF) could offset the thermalization loss of high-energy photons multiexciton generations, thus holding great potential in improving the power conversion efficiency of solar cells. However, the development of SF-based devices has basically remained stagnant so far owing to the limited scope of practical SF materials. Therefore, designing and developing practical SF material systems have been imperative, yet challenging so far. In this work, we comprehensively investigated the effects of aromatic substituents on excited-state properties and SF process of azaquinodimethane systems. Results indicated that the aromatic substituents have a significant influence on molecular diradical characters, thereby determining the excited-state energetics of the SF material system, including optical band gaps and triplet energy. Moreover, the aromatic substituents influenced charge transfer coupling interactions by adjusting molecular packing in the aggregate state to shunt the excited-state population to exert SF process or trap in excimer species. These results not only offer a deep insight into the multiple regulatory effects of the aromatic substituents on excited-state properties and SF process but also provide a practical SF material system, which could lay the foundation for the discovery of new SF-active chromophores and practical applications of new-generation light-harvesting materials.
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http://dx.doi.org/10.1039/d4sc06494a | DOI Listing |
Chemistry
March 2025
Laboratoire de Chimie Supramoléculaire, Institut de Science et d'Ingénierie Supramoléculaires (ISIS), Université de Strasbourg, 8 allée Gaspard Monge, BP 70028, F-67000, Strasbourg Cedex, France.
The conjugation-driven stability and reactivity of bis-imine formation from the reaction of substituted aromatic aldehydes and amines bearing electron donor and acceptor groups were studied in two approaches involving aldehydes and amines with the substituents either conjugated (para position) or non-conjugated (meta position) to the reacting functional groups. The bis-imine from the reaction of a bis-amine (B) with different types of aldehydes (A) constituted an ABA module, whereas the reaction of bis-aldehydes with different amines resulted in a BAB module. The competitive reactions were also studied for a specified bis-amine (B1 or B2) in similar conditions with a mixture of different aldehydes, and the time-dependent generations of dynamic covalent libraries were followed.
View Article and Find Full Text PDFJ Am Chem Soc
March 2025
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, Guangdong Basic Research Center of Excellence for Functional Molecular Engineering, School of Chemistry, IGCME, Sun Yat-sen University, Guangzhou 510275, China.
Nitroso compounds, R-N═O, containing N═O double bonds are ubiquitous and widely utilized in organic synthesis. In contrast, heavier congeners of nitroso compounds, namely pnictinidene chalcogenides R-Pn = E (Pn = P, As, Sb, Bi; E = O, S, Se, Te), are highly reactive and scarce. They have been stabilized in the coordination sphere of Lewis acid/base or by pronounced contribution from resonance structures, whereas free species with unperturbed pnictogen-chalcogen double bonds remains elusive.
View Article and Find Full Text PDFRSC Med Chem
February 2025
School of Chemistry, Faculty of Science, The University of Sydney Sydney New South Wales 2006 Australia
The translocator protein (TSPO) is an 18 kDa protein on the outer mitochondrial membrane. It has gained significant interest in recent years for its potential as a therapeutic target and imaging biomarker, particularly in neuroinflammation, cancer, and central nervous system disorders (CNS). Clinical translation of ligands has been complicated by the presence of a common single nucleotide polymorphism (A147T TSPO), at which many disclosed TSPO ligands lose affinity.
View Article and Find Full Text PDFACS Omega
March 2025
N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Ave. 47, Moscow 119991, Russian Federation.
The interaction of perfluoroaromatic compounds with 1-aminoadamantane followed by oxidation of the formed -adamantylanilines with -chloroperoxybenzoic acid led to functionalized -polyfluorophenyl--adamantylaminoxyls (mono- and diradicals) in high total yields. The molecular and crystal structures of -adamantylanilines and the aminoxyl radicals obtained from them by oxidation have been established using single-crystal X-ray diffraction analysis. The introduction of a substituent into the polyfluorinated moiety affects the arrangement of -adamantylanilines in the crystal structure and the formation of hydrogen bonds; in addition, short contacts of the rare N···N type are present in crystals of 4-((adamantan-1-yl)amino)-perfluorobiphenyl.
View Article and Find Full Text PDFJ Mol Graph Model
March 2025
School of Physics and Physical Engineering, Qufu Normal University, Qufu, 273165, PR China.
Thieno-guanine (thG) is a prominent emissive surrogate of natural guanine (G), which almost perfectly mimics G in nucleic duplexes. In this paper, to widen the utility of thG, the C7 attachment effects by aromatic pyrrole, indole, furan, benzofuran, thiophene, benzothiophene, and pyrene on the structural, electronic, and photophysical properties of thG were theoretically examined by using the density functional theory (DFT) and the time-dependent DFT (TD-DFT). Calculations were performed employing the hybrid B3LYP and the long-range corrected CAM-B3LYP density functionals in combination with the 6-311++G(d, p) basis set.
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