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Science and Technology of Advanced Materials|November 24, 2016
Tetrathiapentalene-based organic conductorsYohji MisakiOrganic Letters|July 20, 2013
[5]Radialene-fused tetrathiafulvalenes exhibiting a simultaneous four- or eight-electron transferMasafumi Ueda, Yohji MisakiChemical Record (New York, N.Y.)|June 4, 2021
Periphery Modification of Tetrathiafulvalenes: Recent Development and ApplicationsAya Yoshimura, Yohji MisakiThe Journal of Organic Chemistry|May 31, 1996
Novel Bis-Fused pi-Electron Donors for Organic Metals: 2-(1,3-Dithiol-2-ylidene)-5-(thiopyran-4-ylidene)-1,3,4,6-tetrathiapentaleneYohji Misaki, Hideki Fujiwara, Tokio YamabeChemsuschem|February 26, 2026
Expanding the Molecular Library for In Situ Polymerization: Design and Evaluation of Dithiafulvene- and Triphenylamine-Based Cathode MaterialsShuntaro Asari, Aya Yoshimura, Takashi Shirahata, et al.Organic Letters|December 10, 2016
Bis- and Tris-fused Tetrathiafulvalenes Extended with Anthracene-9,10-diylideneDaisuke Ogi, Yusuke Fujita, Shigeki Mori, et al.Chemical Communications (Cambridge, England)|October 18, 2023
A triad molecular conductor: simultaneous control of charge and molecular arrangementsNaoya Kinoshita, Atsuya Maruyama, Takashi Shirahata, et al.Organic Letters|August 22, 2018
Redox-Switchable Bis-fused Tetrathiafulvalene Analogue: Observation and Control of Two Different Reduction Processes from Dication to Neutral StateMinami Kato, Yusuke Fujita, Tomokazu Yamauchi, et al.Chemsuschem|July 28, 2025
Molecular Anions Move Faster than Lithium Ions as Charge Carriers in the Organic Battery Electrodes: Insights from 2,6-Bis(diphenylamino)anthraquinoneHikaru Sano, Aya Yoshimura, Masaki Sawada, et al.Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry|September 21, 2025
Anthraquinone Derivatives with Diphenylamino or Carbazole Groups: Organic Active Materials for Use in Lithium-Ion BatteriesAya Yoshimura, Hikaru Sano, Masato Fujimura, et al.Pageof 3