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Tetsuro Kusamoto

Researcher at Graduate University for Advanced Studies

Publications -  83
Citations -  2237

Tetsuro Kusamoto is an academic researcher from Graduate University for Advanced Studies. The author has contributed to research in topics: Radical & Luminescence. The author has an hindex of 22, co-authored 75 publications receiving 1622 citations. Previous affiliations of Tetsuro Kusamoto include University of Tokyo & National Presto Industries.

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Redox Control and High Conductivity of Nickel Bis(dithiolene) Complex π‑Nanosheet: A Potential Organic Two-Dimensional Topological Insulator

TL;DR: This work provides a foothold for the development of the first organic-based two-dimensional topological insulator, which will require the precise control of the oxidation state in the single-layer nickel bisdithiolene complex nanosheet.
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Luminescence, Stability, and Proton Response of an Open‐Shell (3,5‐Dichloro‐4‐pyridyl)bis(2,4,6‐trichlorophenyl)methyl Radical

TL;DR: A luminescent open-shell organic radical with high chemical stability was synthesized and the pyridine moiety acts as a proton coordination site, thereby allowing for control of the electronic and optical properties of the radical by protonation and deprotonation.
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Versatile synthesis of blue luminescent siloles and germoles and hydrogen-bond-assisted color alteration

TL;DR: A variety of dibenzosiloles and -germoles as well as dithiophenosilole (VII) are prepared, better tolerating the functional groups as the methods applied so far.
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Bis(aminothiolato)nickel nanosheet as a redox switch for conductivity and an electrocatalyst for the hydrogen evolution reaction

TL;DR: Precisely tuned functional coordination nanosheet exhibits competent catalytic activity for HER, accompany with drastic electronic property switching by redox treatment.
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Interfacial Synthesis of Electrically Conducting Palladium Bis(dithiolene) Complex Nanosheet.

TL;DR: The synthesis of palladium bis(dithiolene) complex nanosheets (PdDt) possessing a kagome-type lattice structure was performed via interfacial reaction between metal salt in aqueous phase and dithiolato ligand in organic phase.