机构:
Univ St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, ScotlandUniv St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
Wang, Jingxiang
[1
]
Oviedo Ortiz, Jhon Sebastian
论文数: 0引用数: 0
h-index: 0
机构:
Univ Rennes, CNRS, ISCR Inst Sci Chim Rennes, UMR 6226, F-35000 Rennes, FranceUniv St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
Oviedo Ortiz, Jhon Sebastian
[2
]
McKay, Aidan P.
论文数: 0引用数: 0
h-index: 0
机构:
Univ St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, ScotlandUniv St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
McKay, Aidan P.
[1
]
Cordes, David B.
论文数: 0引用数: 0
h-index: 0
机构:
Univ St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, ScotlandUniv St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
Cordes, David B.
[1
]
Crassous, Jeanne
论文数: 0引用数: 0
h-index: 0
机构:
Univ Rennes, CNRS, ISCR Inst Sci Chim Rennes, UMR 6226, F-35000 Rennes, FranceUniv St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
Crassous, Jeanne
[2
]
Zysman-Colman, Eli
论文数: 0引用数: 0
h-index: 0
机构:
Univ St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, ScotlandUniv St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
Zysman-Colman, Eli
[1
]
机构:
[1] Univ St Andrews, Organ Semicond Ctr, EaStCHEM Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[2] Univ Rennes, CNRS, ISCR Inst Sci Chim Rennes, UMR 6226, F-35000 Rennes, France
Multi-resonant thermally activated delayed fluorescence (MR-TADF) helicenes show great potential as chiral emitters due to their typically high photoluminescence quantum yield and that they emit circularly polarized luminescence. Here, a new propeller-shaped chiral MR-TADF helicene DiKTa3, integrating three DiKTa moieties, was designed and synthesized aiming to achieve co-parallel electronic and magnitude transition dipole moments that would lead to a high dissymmetry factor, g. It emits at lambda PL of 491 nm, with a full width at half maximum of 52 nm and has a moderate Delta EST value of 0.24 eV in toluene. The separated (P,P,P) enantiomer shows an absorption dissymmetry factor |gabs| of 6.8x10-4 at 450 nm, which results from a lower symmetry conformation adopted by the compound in solution than the C3-symmetric optimized structure. This work highlights the strong influence that geometry can have on the chiroptical properties of the emitter.