Relationship between the Molecular Geometry and the Radiative Efficiency in Naphthyl-Based Bis-Ortho-Carboranyl Luminophores

• Published in: Molecules (Basel, Switzerland) Switzerland), 2022-10, Vol.27 (19), p.6565
• Main Authors: Yi, Sanghee, Kim, Mingi, Ryu, Chan Hee, You, Dong Kyun, Seo, Yung Ju, Lee, Kang Mun
• Format: Article
• Language: English
• Subjects: Analysis; Cages; Carborane; Charge efficiency; Charge transfer; Chromatography; closo-ortho-carborane; Composition; Crystallography; Decay; Dielectric films; Efficiency; Emission analysis; Geometry; Hydrocarbons; intramolecular charge transfer; Molecular structure; Naphthalene; NMR; Nuclear magnetic resonance; Orthogonality; Quantum efficiency; radiative decay; Solvents; Thin films; X-ray crystallography
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules27196565

The efficiency of intramolecular charge transfer (ICT)-based emission on π-aromatic-group-appended closo-ortho-carboranyl luminophores is known to be affected by structural fluctuations and molecular geometry, but investigation of this relationship has been in progress to date. In this study, four naphthyl-based bis-o-carboranyl compounds, in which hydrogen (15CH and 26CH) or trimethysilyl groups (15CS and 26CS) were appended at the o-carborane cage, were synthesized and fully characterized. All the compounds barely displayed an emissive trace in solution at 298 K; however, 15CH and 26CH distinctly exhibited a dual emissive pattern in rigid states (in solution at 77 K and in films), attributed to locally excited (LE) and ICT-based emission, while 15CS and 26CS showed strong ICT-based greenish emission. Intriguingly, the molecular structures of the four compounds, analyzed by single X-ray crystallography, showed that the C-C bond axis of the o-carborane cage in the trimethysilyl group-appended compounds 15CS and 26CS were more orthogonal to the plane of the appended naphthyl group than those in 15CH and 26CH. These features indicate that 15CS and 26CS present an efficient ICT transition based on strong exo-π-interaction, resulting in a higher quantum efficiency (Φem) for ICT-based radiative decay than those of 15CH and 26CH. Moreover, the 26CS structure revealed most orthogonal geometry, resulting in the highest Φem and lowest knr values for the ICT-based emission. Consequently, all the findings verified that efficient ICT-based radiative decay of aromatic group-appended o-carboranyl luminophores could be achieved by the formation of a specific geometry between the o-carborane cage and the aromatic plane.