Search Results - "Kushida, Tomokatsu"

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  1. 1

    A Radical Anion of Structurally Constrained Triphenylborane by Kushida, Tomokatsu, Yamaguchi, Shigehiro

    Published in Organometallics (25-11-2013)
    “…Chemical reduction of the structurally constrained triphenylborane 1 with K produced a radical anion. EPR analysis demonstrated the delocalization of the…”
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  2. 2

    Mixed-Orbital Charge Transport in N‑Shaped Benzene- and Pyrazine-Fused Organic Semiconductors by Yu, Craig P., Kumagai, Shohei, Kushida, Tomokatsu, Mitani, Masato, Mitsui, Chikahiko, Ishii, Hiroyuki, Takeya, Jun, Okamoto, Toshihiro

    Published in Journal of the American Chemical Society (29-06-2022)
    “…The hole-carrier transport of organic semiconductors is widely known to occur via intermolecular orbital overlaps of the highest occupied molecular orbitals…”
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  3. 3

    Photochemical Intramolecular C−H Addition of Dimesityl(hetero)arylboranes through a [1,6]‐Sigmatropic Rearrangement by Ando, Naoki, Fukazawa, Aiko, Kushida, Tomokatsu, Shiota, Yoshihito, Itoyama, Shuhei, Yoshizawa, Kazunari, Matsui, Yasunori, Kuramoto, Yutaro, Ikeda, Hiroshi, Yamaguchi, Shigehiro

    Published in Angewandte Chemie International Edition (25-09-2017)
    “…A new reaction mode for triarylboranes under photochemical conditions was discovered. Photoirradiation of dimesitylboryl‐substituted (hetero)arenes produced…”
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    Journal Article
  4. 4

    Planarized B-phenylborataanthracene anions: structural and electronic impacts of coplanar constraint by Kushida, Tomokatsu, Zhou, Zhiguo, Wakamiya, Atsushi, Yamaguchi, Shigehiro

    “…Potassium and lithium salts of anionic B-phenylborataanthracenes, whose phenyl groups were fixed in a coplanar fashion, were synthesized. These compounds…”
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  5. 5

    Synthesis and Reversible Control of the Fluorescent Properties of a Divalent Tin Dipyrromethene by Kobayashi, Junji, Kushida, Tomokatsu, Kawashima, Takayuki

    Published in Journal of the American Chemical Society (12-08-2009)
    “…A fluorescent chlorostannylene bearing a dipyrromethene ligand was synthesized. Its fluorescence quantum yield was low, Φf = 0.04, probably because of the…”
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  6. 6

    Constraint-induced structural deformation of planarized triphenylboranes in the excited state by Kushida, Tomokatsu, Camacho, Cristopher, Shuto, Ayumi, Irle, Stephan, Muramatsu, Masayasu, Katayama, Tetsuro, Ito, Syoji, Nagasawa, Yutaka, Miyasaka, Hiroshi, Sakuda, Eri, Kitamura, Noboru, Zhou, Zhiguo, Wakamiya, Atsushi, Yamaguchi, Shigehiro

    Published in Chemical science (Cambridge) (01-01-2014)
    “…Triphenylboranes planarized with three methylene bridges exhibited dual fluorescence bands around 340 and 400 nm despite their structural constraint. To…”
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  7. 7

    Control of molecular doping in conjugated polymers by thermal annealing by Fujimoto, Ryo, Watanabe, Shun, Yamashita, Yu, Tsurumi, Junto, Matsui, Hiroyuki, Kushida, Tomokatsu, Mitsui, Chikahiko, Yi, Hee Taek, Podzorov, Vitaly, Takeya, Jun

    Published in Organic electronics (01-08-2017)
    “…Doping is one of the most fundamental building blocks for semiconductor processing, and enables adaptation to both charge concentration and electrical…”
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  8. 8

    Planarized Triarylboranes: Stabilization by Structural Constraint and Their Plane-to-Bowl Conversion by Zhou, Zhiguo, Wakamiya, Atsushi, Kushida, Tomokatsu, Yamaguchi, Shigehiro

    Published in Journal of the American Chemical Society (14-03-2012)
    “…Triphenylborane and 9,10-diphenyl-9,10-dihydro-9,10-diboraanthracene, constrained to a planar arrangement with methylene tethers, were synthesized by…”
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  9. 9

    A Planarized Triphenylborane Mesogen: Discotic Liquid Crystals with Ambipolar Charge-Carrier Transport Properties by Kushida, Tomokatsu, Shuto, Ayumi, Yoshio, Masafumi, Kato, Takashi, Yamaguchi, Shigehiro

    Published in Angewandte Chemie International Edition (01-06-2015)
    “…A discotic liquid‐crystalline (LC) material, consisting of a planarized triphenylborane mesogen, was synthesized. X‐ray diffraction analysis confirmed that…”
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  10. 10

    Boracyclophanes: Modulation of the σ/π Character in Boron-Benzene Interactions by Kushida, Tomokatsu, Yamaguchi, Shigehiro

    Published in Angewandte Chemie International Edition (29-07-2013)
    “…Character sketch: Boracyclophanes, in which the benzene ring coordinates to the boron atom, were synthesized. X‐ray crystallographic analysis and theoretical…”
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  11. 11

    π‑Extended Planarized Triphenylboranes with Thiophene Spacers by Shuto, Ayumi, Kushida, Tomokatsu, Fukushima, Tatsuya, Kaji, Hironori, Yamaguchi, Shigehiro

    Published in Organic letters (20-12-2013)
    “…Planarized triphenylboranes extended with thiophene or bithiophene spacers were synthesized, which showed intense fluorescences in solution and reversible…”
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  12. 12

    Fluorescent Organic π‐Radicals Stabilized with Boron: Featuring a SOMO–LUMO Electronic Transition by Ito, Masato, Shirai, Shusuke, Xie, Yongfa, Kushida, Tomokatsu, Ando, Naoki, Soutome, Hiroki, Fujimoto, Kazuhiro J., Yanai, Takeshi, Tabata, Kenichi, Miyata, Yasuo, Kita, Hiroshi, Yamaguchi, Shigehiro

    Published in Angewandte Chemie International Edition (20-06-2022)
    “…We report on the fluorescence properties of a new class of emissive and stable π‐radicals that contain a boron atom at a position distant from the radical…”
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  13. 13

    Boron-Stabilized Planar Neutral π‑Radicals with Well-Balanced Ambipolar Charge-Transport Properties by Kushida, Tomokatsu, Shirai, Shusuke, Ando, Naoki, Okamoto, Toshihiro, Ishii, Hiroyuki, Matsui, Hiroyuki, Yamagishi, Masakazu, Uemura, Takafumi, Tsurumi, Junto, Watanabe, Shun, Takeya, Jun, Yamaguchi, Shigehiro

    Published in Journal of the American Chemical Society (18-10-2017)
    “…Organic neutral π-monoradicals are promising semiconductors with balanced ambipolar carrier-transport abilities, which arise from virtually identical spatial…”
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  14. 14

    Boracyclophanes: Modulation of the [sigma]/[pi]Character in Boron-Benzene Interactions by Kushida, Tomokatsu, Yamaguchi, Shigehiro

    Published in Angewandte Chemie International Edition (29-07-2013)
    “…Character sketch: Boracyclophanes, in which the benzene ring coordinates to the boron atom, were synthesized. X-ray crystallographic analysis and theoretical…”
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    Journal Article
  15. 15
  16. 16

    Boracyclophanes: Modulation of the σ/π Character in Boron-Benzene Interactions by Kushida, Tomokatsu, Yamaguchi, Shigehiro

    Published in Angewandte Chemie (29-07-2013)
    “…Charakterzeichnung: Boracyclophane, in denen der Benzolring an das Boratom koordiniert, wurden synthetisiert. Die Eigenschaften der Bor‐Benzol‐Wechselwirkung…”
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  17. 17

    Fluorescent Organic π‐Radicals Stabilized with Boron: Featuring a SOMO–LUMO Electronic Transition by Ito, Masato, Shirai, Shusuke, Xie, Yongfa, Kushida, Tomokatsu, Ando, Naoki, Soutome, Hiroki, Fujimoto, Kazuhiro J., Yanai, Takeshi, Tabata, Kenichi, Miyata, Yasuo, Kita, Hiroshi, Yamaguchi, Shigehiro

    Published in Angewandte Chemie (20-06-2022)
    “…We report on the fluorescence properties of a new class of emissive and stable π‐radicals that contain a boron atom at a position distant from the radical…”
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    Journal Article
  18. 18
  19. 19

    A Planarized Triphenylborane Mesogen: Discotic Liquid Crystals with Ambipolar Charge-Carrier Transport Properties by Kushida, Tomokatsu, Shuto, Ayumi, Yoshio, Masafumi, Kato, Takashi, Yamaguchi, Shigehiro

    Published in Angewandte Chemie (01-06-2015)
    “…A discotic liquid‐crystalline (LC) material, consisting of a planarized triphenylborane mesogen, was synthesized. X‐ray diffraction analysis confirmed that…”
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    Journal Article
  20. 20

    Photochemical Intramolecular C−H Addition of Dimesityl(hetero)arylboranes through a [1,6]‐Sigmatropic Rearrangement by Ando, Naoki, Fukazawa, Aiko, Kushida, Tomokatsu, Shiota, Yoshihito, Itoyama, Shuhei, Yoshizawa, Kazunari, Matsui, Yasunori, Kuramoto, Yutaro, Ikeda, Hiroshi, Yamaguchi, Shigehiro

    Published in Angewandte Chemie (25-09-2017)
    “…A new reaction mode for triarylboranes under photochemical conditions was discovered. Photoirradiation of dimesitylboryl‐substituted (hetero)arenes produced…”
    Get full text
    Journal Article