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Soichiro Nakatsuka

Researcher at Kwansei Gakuin University

Publications -  25
Citations -  2122

Soichiro Nakatsuka is an academic researcher from Kwansei Gakuin University. The author has contributed to research in topics: OLED & Chemistry. The author has an hindex of 11, co-authored 20 publications receiving 1371 citations.

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Ultrapure Blue Thermally Activated Delayed Fluorescence Molecules: Efficient HOMO–LUMO Separation by the Multiple Resonance Effect

TL;DR: Ultrapure blue-fluorescent molecules based on thermally activated delayed fluorescence are developed that exhibit a deep blue emission at 467 nm with a full-width at half-maximum of 28 nm and an internal quantum efficiency of ≈100%, which represent record-setting performance for blue OLED devices.
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One-Step Borylation of 1,3-Diaryloxybenzenes Towards Efficient Materials for Organic Light-Emitting Diodes

TL;DR: The development of a one-step borylation of 1,3-diaryloxybenzenes is reported, yielding novel boron-containing polycyclic aromatic compounds, which possess high singlet-triplet excitation energies as a result of localized frontier molecular orbitals induced by bor on and oxygen.
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Two-Step Synthesis of Boron-Fused Double Helicenes.

TL;DR: Novel boron-fused double [5]helicenes were synthesized from hexabromobenzene in two steps via Hart reaction and demethylative cyclization, enabling optical resolution and excellent ambipolar conductivity.
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Multiple heteroatom substitution to graphene nanoribbon

TL;DR: This work synthesized multiple heteroatom-substituted graphene nanoribbons and showed that AFM can directly resolve elemental differences and can be correlated to the van der Waals radii, as well as the modulated local electron density caused by the substitution.
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Divergent Synthesis of Heteroatom-Centered 4,8,12-Triazatriangulenes.

TL;DR: A divergent synthesis of heteroatom-centered 4,8,12-triazatriangulenes was explored, which involved the preparation of a nitrogen-containing macrocyclic precursor and subsequent central heteroatoms introduction by electrophilic C-Li and C-H substitution.