Tomohiko Nishiuchi

Assistant Professor

Osaka University

Japan

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About

Tomohiko Nishiuchi is an Assistant Professor at Osaka University, Japan. His research areas include photomechanical materials, surface synthesis of organic compounds, and molecular quantum systems, as reflected in his recent publications. His work explores the interplay between theoretical and experimental approaches in the synthesis and reactivity of novel molecular structures.

Articles (20)

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2025

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2022

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2022

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2022

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2022

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2022

Collaborators (12)

Gregory Beran

Professor

University of California, Riverside

UNITED STATES

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Samuel Jeong

Assistant Professor

University of Tsukuba

JAPAN

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Ryohei Kishi

Associate Professor

JAPAN

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Tatsuhiko Ohto

Associate Professor

Nagoya University

JAPAN

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Jose Lado

Assistant Professor

Aalto University

FINLAND

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Hajime Kimizuka

Professor

Nagoya University

JAPAN

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Orlando Silveira

Aalto University

FINLAND

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Yoshikazu Ito

Associate Professor

University of Tsukuba

JAPAN

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Yasufumi Takahashi

Nagoya University

JAPAN

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Veronica Carta

University of California, Riverside

UNITED STATES

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Shohei Saito

准教授 / Associate Professor

Kyoto University

JAPAN

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Takashi Kubo

Professor

Osaka University

JAPAN

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Tomohiko Nishiuchi

Research Interests

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About

Articles (20)

Photomechanical Anthracenophane Crystals: Theory, Experiment, and Composite Actuator Performance

Pyrrole-Fused Aza-Nanographene with Two Gulf-Edge Regions as Flexible Sites

Frustration-Induced Many-Body Degeneracy in Spin −1/2 Molecular Quantum Rings

Using an aromatic linker to optimize charge-resonance states, photodimerization and reversibility in covalent anthracene dimers

Systematic C–C Bond Cleavage in Oligomers via Diels–Alder Reaction on Au(111)

Synthesis and reactivity of the di(9-anthryl)methyl radical

On‐Surface Synthesis of Silole and Disila‐Cyclooctene Derivatives

Back Cover: On‐Surface Synthesis of Silole and Disila‐Cyclooctene Derivatives (Angew. Chem. Int. Ed. 18/2024)

On‐Surface Synthesis of Silole and Disila‐Cyclooctene Derivatives

Rücktitelbild: On‐Surface Synthesis of Silole and Disila‐Cyclooctene Derivatives (Angew. Chem. 18/2024)

Suppression of Methanol and Formate Crossover through Sulfanilic‐Functionalized Holey Graphene as Proton Exchange Membranes

1T/1H-SnS2 Sheets for Electrochemical CO2 Reduction to Formate

Stacked antiaromaticity in the π‐congested space between the aromatic rings in the anthracene dimer

Synthesis and structural evaluation of closed-shell folded and open-shell twisted hexabenzo[5.6.7]quinarene

Computational Study of the Effect of π-Congestion on the Singlet Biradical Character and Stacked Antiaromaticity in Acene Dimers

Stacked Antiaromaticity in the π-Congested Space Between the Aromatic Rings in the Anthracene Dimer

Stacked 3D Antiaromaticity in the π-Congested Space Between the Aromatic Rings in the Anthracene Dimer

Cover Feature: Sterically Frustrated Aromatic Enes with Various Colors Originating from Multiple Folded and Twisted Conformations in Crystal Polymorphs (Chem. Eur. J. 28/2022)

Sterically Frustrated Aromatic Enes with Various Colors Originating from Multiple Folded and Twisted Conformations in Crystal Polymorphs**

Synthesis of π-Extended Thiele’s and Chichibabin’s Hydrocarbons and Effect of the π-Congestion on Conformations and Electronic States

Collaborators (12)

Gregory Beran

Samuel Jeong

Ryohei Kishi

Tatsuhiko Ohto

Jose Lado

Hajime Kimizuka

Orlando Silveira

Yoshikazu Ito

Yasufumi Takahashi

Veronica Carta

Shohei Saito

Takashi Kubo

Make your next move.

Tomohiko Nishiuchi

Research Interests

Explore related searches

Contact this professor

About

Articles (20)

Photomechanical Anthracenophane Crystals: Theory, Experiment, and Composite Actuator Performance

Pyrrole-Fused Aza-Nanographene with Two Gulf-Edge Regions as Flexible Sites

Frustration-Induced Many-Body Degeneracy in Spin −1/2 Molecular Quantum Rings

Using an aromatic linker to optimize charge-resonance states, photodimerization and reversibility in covalent anthracene dimers

Systematic C–C Bond Cleavage in Oligomers via Diels–Alder Reaction on Au(111)

Synthesis and reactivity of the di(9-anthryl)methyl radical

On‐Surface Synthesis of Silole and Disila‐Cyclooctene Derivatives

Back Cover: On‐Surface Synthesis of Silole and Disila‐Cyclooctene Derivatives (Angew. Chem. Int. Ed. 18/2024)

On‐Surface Synthesis of Silole and Disila‐Cyclooctene Derivatives

Rücktitelbild: On‐Surface Synthesis of Silole and Disila‐Cyclooctene Derivatives (Angew. Chem. 18/2024)

Suppression of Methanol and Formate Crossover through Sulfanilic‐Functionalized Holey Graphene as Proton Exchange Membranes

1T/1H-SnS2 Sheets for Electrochemical CO2 Reduction to Formate

Stacked antiaromaticity in the π‐congested space between the aromatic rings in the anthracene dimer

Synthesis and structural evaluation of closed-shell folded and open-shell twisted hexabenzo[5.6.7]quinarene

Computational Study of the Effect of &pi;-Congestion on the Singlet Biradical Character and Stacked Antiaromaticity in Acene Dimers

Stacked Antiaromaticity in the &pi;-Congested Space Between the Aromatic Rings in the Anthracene Dimer

Stacked 3D Antiaromaticity in the &pi;-Congested Space Between the Aromatic Rings in the Anthracene Dimer

Cover Feature: Sterically Frustrated Aromatic Enes with Various Colors Originating from Multiple Folded and Twisted Conformations in Crystal Polymorphs (Chem. Eur. J. 28/2022)

Sterically Frustrated Aromatic Enes with Various Colors Originating from Multiple Folded and Twisted Conformations in Crystal Polymorphs**

Synthesis of π-Extended Thiele’s and Chichibabin’s Hydrocarbons and Effect of the π-Congestion on Conformations and Electronic States

Collaborators (12)

Gregory Beran

Samuel Jeong

Ryohei Kishi

Tatsuhiko Ohto

Jose Lado

Hajime Kimizuka

Orlando Silveira

Yoshikazu Ito

Yasufumi Takahashi

Veronica Carta

Shohei Saito

Takashi Kubo

Make your next move.

Computational Study of the Effect of π-Congestion on the Singlet Biradical Character and Stacked Antiaromaticity in Acene Dimers

Stacked Antiaromaticity in the π-Congested Space Between the Aromatic Rings in the Anthracene Dimer

Stacked 3D Antiaromaticity in the π-Congested Space Between the Aromatic Rings in the Anthracene Dimer