齊藤 尚平

Last Update: 2018/08/03 12:49:27

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Name(Kanji/Kana/Abecedarium Latinum)
齊藤 尚平/サイトウ シヨウヘイ/Saito, Shohei
Primary Affiliation(Org1/Job title)
Graduate Schools Science/Associate Professor
Faculty
Org1 Job title
理学部
Academic Degree
Field(Japanese) Field(English) University(Japanese) University(English) Method
修士(理学) 京都大学
博士(理学) 京都大学
Graduate School
University(Japanese) University(English) Faculty(Japanese) Faculty(English) Major(Japanese) Major(English) Degree
京都大学 大学院理学研究科修士課程化学専攻 修了
京都大学 大学院理学研究科博士後期課程化学専攻 修了
Undergraduate School / Major(s)
University(Japanese) University(English) Faculty(Japanese) Faculty(English) Major(s)(Japanese) Major(s)(English) Degree
京都大学 理学部理学科 卒業
High School
Highschool Kana
私立武蔵高校
Personal Website(s) (URL(s))
URL
http://shohei-saito.webnode.jp
ORCID ID
https://orcid.org/0000-0003-1863-9956
researchmap URL
https://researchmap.jp/read0156671
Published Papers
Author Author(Japanese) Author(English) Title Title(Japanese) Title(English) Bibliography Bibliography(Japanese) Bibliography(English) Publication date Refereed paper Language Publishing type Disclose
Eduard Carbonell-Sanrom{\`{a}}, Aran Garcia-Lekue, Martina Corso, Guillaume Vasseur, Pedro Brandimarte, Jorge Lobo-Checa, Dimas G. de Oteyza, Jingcheng Li, Shigeki Kawai, Shohei Saito, Shigehiro Yamaguchi, J. Enrique Ortega, Daniel S{\'{a}}nchez-Portal, Jose Ignacio Pascual Eduard Carbonell-Sanrom{\`{a}}, Aran Garcia-Lekue, Martina Corso, Guillaume Vasseur, Pedro Brandimarte, Jorge Lobo-Checa, Dimas G. de Oteyza, Jingcheng Li, Shigeki Kawai, Shohei Saito, Shigehiro Yamaguchi, J. Enrique Ortega, Daniel S{\'{a}}nchez-Portal, Jose Ignacio Pascual Eduard Carbonell-Sanrom{\`{a}}, Aran Garcia-Lekue, Martina Corso, Guillaume Vasseur, Pedro Brandimarte, Jorge Lobo-Checa, Dimas G. de Oteyza, Jingcheng Li, Shigeki Kawai, Shohei Saito, Shigehiro Yamaguchi, J. Enrique Ortega, Daniel S{\'{a}}nchez-Portal, Jose Ignacio Pascual Electronic Properties of Substitutionally Boron-Doped Graphene Nanoribbons on a Au(111) Surface Electronic Properties of Substitutionally Boron-Doped Graphene Nanoribbons on a Au(111) Surface Electronic Properties of Substitutionally Boron-Doped Graphene Nanoribbons on a Au(111) Surface The Journal of Physical Chemistry C The Journal of Physical Chemistry C The Journal of Physical Chemistry C 2018/07 Refereed Disclose to all
Takuya Yamakado, Kazuya Otsubo, Atsuhiro Osuka, Shohei Saito Takuya Yamakado, Kazuya Otsubo, Atsuhiro Osuka, Shohei Saito Takuya Yamakado, Kazuya Otsubo, Atsuhiro Osuka, Shohei Saito Compression of a Flapping Mechanophore Accompanied by Thermal Void Collapse in a Crystalline Phase Compression of a Flapping Mechanophore Accompanied by Thermal Void Collapse in a Crystalline Phase Compression of a Flapping Mechanophore Accompanied by Thermal Void Collapse in a Crystalline Phase Journal of the American Chemical Society Journal of the American Chemical Society Journal of the American Chemical Society 2018/05 Refereed Disclose to all
Fumitoshi Ema, Mana Tanabe, Shohei Saito, Tomoki Yoneda, Kenji Sugisaki, Takashi Tachikawa, Seiji Akimoto, Seigo Yamauchi, Kazunobu Sato, Atsuhiro Osuka, Takeji Takui, Yasuhiro Kobori Fumitoshi Ema, Mana Tanabe, Shohei Saito, Tomoki Yoneda, Kenji Sugisaki, Takashi Tachikawa, Seiji Akimoto, Seigo Yamauchi, Kazunobu Sato, Atsuhiro Osuka, Takeji Takui, Yasuhiro Kobori Fumitoshi Ema, Mana Tanabe, Shohei Saito, Tomoki Yoneda, Kenji Sugisaki, Takashi Tachikawa, Seiji Akimoto, Seigo Yamauchi, Kazunobu Sato, Atsuhiro Osuka, Takeji Takui, Yasuhiro Kobori Charge-Transfer Character Drives Möbius Antiaromaticity in the Excited Triplet State of Twisted [28]Hexaphyrin Charge-Transfer Character Drives Möbius Antiaromaticity in the Excited Triplet State of Twisted [28]Hexaphyrin Charge-Transfer Character Drives Möbius Antiaromaticity in the Excited Triplet State of Twisted [28]Hexaphyrin The Journal of Physical Chemistry Letters, 2685 The Journal of Physical Chemistry Letters, 2685 The Journal of Physical Chemistry Letters, 2685 2018/05 Refereed Disclose to all
Takuya Yamakado, Shota Takahashi, Kazuya Watanabe, Yoshiyasu Matsumoto, Atsuhiro Osuka, Shohei Saito Takuya Yamakado, Shota Takahashi, Kazuya Watanabe, Yoshiyasu Matsumoto, Atsuhiro Osuka, Shohei Saito Takuya Yamakado, Shota Takahashi, Kazuya Watanabe, Yoshiyasu Matsumoto, Atsuhiro Osuka, Shohei Saito Conformational Planarization versus Singlet Fission: Distinct Excited-State Dynamics of Cyclooctatetraene-Fused Acene Dimers Conformational Planarization versus Singlet Fission: Distinct Excited-State Dynamics of Cyclooctatetraene-Fused Acene Dimers Conformational Planarization versus Singlet Fission: Distinct Excited-State Dynamics of Cyclooctatetraene-Fused Acene Dimers Angewandte Chemie International Edition, 57, 19, 5438 Angewandte Chemie International Edition, 57, 19, 5438 Angewandte Chemie International Edition, 57, 19, 5438 2018/05 Refereed Disclose to all
Takuya Yamakado, Shota Takahashi, Kazuya Watanabe, Yoshiyasu Matsumoto, Atsuhiro Osuka, Shohei Saito Takuya Yamakado, Shota Takahashi, Kazuya Watanabe, Yoshiyasu Matsumoto, Atsuhiro Osuka, Shohei Saito Takuya Yamakado, Shota Takahashi, Kazuya Watanabe, Yoshiyasu Matsumoto, Atsuhiro Osuka, Shohei Saito Conformational Planarization versus Singlet Fission: Distinct Excited-State Dynamics of Cyclooctatetraene-Fused Acene Dimers Conformational Planarization versus Singlet Fission: Distinct Excited-State Dynamics of Cyclooctatetraene-Fused Acene Dimers Conformational Planarization versus Singlet Fission: Distinct Excited-State Dynamics of Cyclooctatetraene-Fused Acene Dimers Angewandte Chemie, 130, 19, 5536 Angewandte Chemie, 130, 19, 5536 Angewandte Chemie, 130, 19, 5536 2018/05 Refereed Disclose to all
Masaki Hada, Shohei Saito, Sei'ichi Tanaka, Ryuma Sato, Masahiko Yoshimura, Kazuhiro Mouri, Kyohei Matsuo, Shigehiro Yamaguchi, Mitsuo Hara, Yasuhiko Hayashi, Fynn Röhricht, Rainer Herges, Yasuteru Shigeta, Ken Onda, R. J. Dwayne Miller Masaki Hada, Shohei Saito, Sei'ichi Tanaka, Ryuma Sato, Masahiko Yoshimura, Kazuhiro Mouri, Kyohei Matsuo, Shigehiro Yamaguchi, Mitsuo Hara, Yasuhiko Hayashi, Fynn Röhricht, Rainer Herges, Yasuteru Shigeta, Ken Onda, R. J. Dwayne Miller Masaki Hada, Shohei Saito, Sei'ichi Tanaka, Ryuma Sato, Masahiko Yoshimura, Kazuhiro Mouri, Kyohei Matsuo, Shigehiro Yamaguchi, Mitsuo Hara, Yasuhiko Hayashi, Fynn Röhricht, Rainer Herges, Yasuteru Shigeta, Ken Onda, R. J. Dwayne Miller Structural Monitoring of the Onset of Excited-State Aromaticity in a Liquid Crystal Phase Structural Monitoring of the Onset of Excited-State Aromaticity in a Liquid Crystal Phase Structural Monitoring of the Onset of Excited-State Aromaticity in a Liquid Crystal Phase Journal of the American Chemical Society, 139, 44, 15792 Journal of the American Chemical Society, 139, 44, 15792 Journal of the American Chemical Society, 139, 44, 15792 2017/11 Refereed Disclose to all
Kotani R, Sotome H, Okajima H, Yokoyama S, Nakaike Y, Kashiwagi A, Mori C, Nakada Y, Yamaguchi S, Osuka A, Sakamoto A, Miyasaka H, Saito S. Kotani R, Sotome H, Okajima H, Yokoyama S, Nakaike Y, Kashiwagi A, Mori C, Nakada Y, Yamaguchi S, Osuka A, Sakamoto A, Miyasaka H, Saito S. Kotani R, Sotome H, Okajima H, Yokoyama S, Nakaike Y, Kashiwagi A, Mori C, Nakada Y, Yamaguchi S, Osuka A, Sakamoto A, Miyasaka H, Saito S. Flapping viscosity probe that shows polarity-independent ratiometric fluorescence Flapping viscosity probe that shows polarity-independent ratiometric fluorescence Flapping viscosity probe that shows polarity-independent ratiometric fluorescence Journal of Materials Chemistry C, 5, 21, 5249-5256 Journal of Materials Chemistry C, 5, 21, 5249-5256 Journal of Materials Chemistry C, 5, 21, 5249-5256 2017 Refereed Disclose to all
Kyohei Matsuo, Shohei Saito, Shigehiro Yamaguchi Kyohei Matsuo, Shohei Saito, Shigehiro Yamaguchi Kyohei Matsuo, Shohei Saito, Shigehiro Yamaguchi A Soluble Dynamic Complex Strategy for the Solution-Processed Fabrication of Organic Thin-Film Transistors of a Boron-Containing Polycyclic Aromatic Hydrocarbon A Soluble Dynamic Complex Strategy for the Solution-Processed Fabrication of Organic Thin-Film Transistors of a Boron-Containing Polycyclic Aromatic Hydrocarbon A Soluble Dynamic Complex Strategy for the Solution-Processed Fabrication of Organic Thin-Film Transistors of a Boron-Containing Polycyclic Aromatic Hydrocarbon Angewandte Chemie, 128, 39, 12163 Angewandte Chemie, 128, 39, 12163 Angewandte Chemie, 128, 39, 12163 2016/08 Refereed Disclose to all
Kyohei Matsuo, Shohei Saito, Shigehiro Yamaguchi Kyohei Matsuo, Shohei Saito, Shigehiro Yamaguchi Kyohei Matsuo, Shohei Saito, Shigehiro Yamaguchi A Soluble Dynamic Complex Strategy for the Solution-Processed Fabrication of Organic Thin-Film Transistors of a Boron-Containing Polycyclic Aromatic Hydrocarbon A Soluble Dynamic Complex Strategy for the Solution-Processed Fabrication of Organic Thin-Film Transistors of a Boron-Containing Polycyclic Aromatic Hydrocarbon A Soluble Dynamic Complex Strategy for the Solution-Processed Fabrication of Organic Thin-Film Transistors of a Boron-Containing Polycyclic Aromatic Hydrocarbon Angewandte Chemie International Edition, 55, 39, 11984 Angewandte Chemie International Edition, 55, 39, 11984 Angewandte Chemie International Edition, 55, 39, 11984 2016/08 Refereed Disclose to all
Hiroshi Osaki, Chih-Ming Chou, Masayasu Taki, Kai Welke, Daisuke Yokogawa, Stephan Irle, Yoshikatsu Sato, Tetsuya Higashiyama, Shohei Saito, Aiko Fukazawa, Shigehiro Yamaguchi Hiroshi Osaki, Chih-Ming Chou, Masayasu Taki, Kai Welke, Daisuke Yokogawa, Stephan Irle, Yoshikatsu Sato, Tetsuya Higashiyama, Shohei Saito, Aiko Fukazawa, Shigehiro Yamaguchi Hiroshi Osaki, Chih-Ming Chou, Masayasu Taki, Kai Welke, Daisuke Yokogawa, Stephan Irle, Yoshikatsu Sato, Tetsuya Higashiyama, Shohei Saito, Aiko Fukazawa, Shigehiro Yamaguchi A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime Angewandte Chemie, 128, 25, 7247 Angewandte Chemie, 128, 25, 7247 Angewandte Chemie, 128, 25, 7247 2016/04 Refereed Disclose to all
Hiroshi Osaki, Chih-Ming Chou, Masayasu Taki, Kai Welke, Daisuke Yokogawa, Stephan Irle, Yoshikatsu Sato, Tetsuya Higashiyama, Shohei Saito, Aiko Fukazawa, Shigehiro Yamaguchi Hiroshi Osaki, Chih-Ming Chou, Masayasu Taki, Kai Welke, Daisuke Yokogawa, Stephan Irle, Yoshikatsu Sato, Tetsuya Higashiyama, Shohei Saito, Aiko Fukazawa, Shigehiro Yamaguchi Hiroshi Osaki, Chih-Ming Chou, Masayasu Taki, Kai Welke, Daisuke Yokogawa, Stephan Irle, Yoshikatsu Sato, Tetsuya Higashiyama, Shohei Saito, Aiko Fukazawa, Shigehiro Yamaguchi A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime Angewandte Chemie International Edition, 55, 25, 7131 Angewandte Chemie International Edition, 55, 25, 7131 Angewandte Chemie International Edition, 55, 25, 7131 2016/04 Refereed Disclose to all
Matsuo K, Saito S, Yamaguchi S. Matsuo K, Saito S, Yamaguchi S. Matsuo K, Saito S, Yamaguchi S. A Soluble Dynamic Complex Strategy for the Solution-Processed Fabrication of Organic Thin-Film Transistors of a Boron-Containing Polycyclic Aromatic Hydrocarbon A Soluble Dynamic Complex Strategy for the Solution-Processed Fabrication of Organic Thin-Film Transistors of a Boron-Containing Polycyclic Aromatic Hydrocarbon A Soluble Dynamic Complex Strategy for the Solution-Processed Fabrication of Organic Thin-Film Transistors of a Boron-Containing Polycyclic Aromatic Hydrocarbon Angewandte Chemie - International Edition, 55, 39, 11984-11988 Angewandte Chemie - International Edition, 55, 39, 11984-11988 Angewandte Chemie - International Edition, 55, 39, 11984-11988 2016 Refereed Disclose to all
Saito S, Nobusue S, Tsuzaka E, Yuan C, Mori C, Hara M, Seki T, Camacho C, Irle S, Yamaguchi S. Saito S, Nobusue S, Tsuzaka E, Yuan C, Mori C, Hara M, Seki T, Camacho C, Irle S, Yamaguchi S. Saito S, Nobusue S, Tsuzaka E, Yuan C, Mori C, Hara M, Seki T, Camacho C, Irle S, Yamaguchi S. Light-melt adhesive based on dynamic carbon frameworks in a columnar liquid-crystal phase Light-melt adhesive based on dynamic carbon frameworks in a columnar liquid-crystal phase Light-melt adhesive based on dynamic carbon frameworks in a columnar liquid-crystal phase Nature Communications, 7 Nature Communications, 7 Nature Communications, 7 2016 Refereed Disclose to all
Osaki H, Chou C.-M, Taki M, Welke K, Yokogawa D, Irle S, Sato Y, Higashiyama T, Saito S, Fukazawa A, Yamaguchi S. Osaki H, Chou C.-M, Taki M, Welke K, Yokogawa D, Irle S, Sato Y, Higashiyama T, Saito S, Fukazawa A, Yamaguchi S. Osaki H, Chou C.-M, Taki M, Welke K, Yokogawa D, Irle S, Sato Y, Higashiyama T, Saito S, Fukazawa A, Yamaguchi S. A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime Angewandte Chemie - International Edition, 55, 25, 7131-7135 Angewandte Chemie - International Edition, 55, 25, 7131-7135 Angewandte Chemie - International Edition, 55, 25, 7131-7135 2016 Refereed Disclose to all
Shinichiro Osumi, Shohei Saito, Chuandong Dou, Kyohei Matsuo, Keita Kume, Hirofumi Yoshikawa, Kunio Awaga, Shigehiro Yamaguchi Shinichiro Osumi, Shohei Saito, Chuandong Dou, Kyohei Matsuo, Keita Kume, Hirofumi Yoshikawa, Kunio Awaga, Shigehiro Yamaguchi Shinichiro Osumi, Shohei Saito, Chuandong Dou, Kyohei Matsuo, Keita Kume, Hirofumi Yoshikawa, Kunio Awaga, Shigehiro Yamaguchi Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance Chem. Sci., 7, 1, 219 Chem. Sci., 7, 1, 219 Chem. Sci., 7, 1, 219 2016 Refereed Disclose to all
Hada M, Saito S, Tanaka S, Sato R, Matsuo K, Hara M, Hayashi Y, Mouri K, Yoshimura M, Shigeta Y, Yamaguchi S, Onda K, Miller R.J.D. Hada M, Saito S, Tanaka S, Sato R, Matsuo K, Hara M, Hayashi Y, Mouri K, Yoshimura M, Shigeta Y, Yamaguchi S, Onda K, Miller R.J.D. Hada M, Saito S, Tanaka S, Sato R, Matsuo K, Hara M, Hayashi Y, Mouri K, Yoshimura M, Shigeta Y, Yamaguchi S, Onda K, Miller R.J.D. Ultrafast snapshots of the molecules twisting in liquid crystal state Ultrafast snapshots of the molecules twisting in liquid crystal state Ultrafast snapshots of the molecules twisting in liquid crystal state Optics InfoBase Conference Papers Optics InfoBase Conference Papers Optics InfoBase Conference Papers 2016 Refereed Disclose to all
Osumi S, Saito S, Dou C, Matsuo K, Kume K, Yoshikawa H, Awaga K, Yamaguchi S. Osumi S, Saito S, Dou C, Matsuo K, Kume K, Yoshikawa H, Awaga K, Yamaguchi S. Osumi S, Saito S, Dou C, Matsuo K, Kume K, Yoshikawa H, Awaga K, Yamaguchi S. Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance Chemical Science, 7, 1, 219-227 Chemical Science, 7, 1, 219-227 Chemical Science, 7, 1, 219-227 2015 Refereed Disclose to all
Kawai S, Saito S, Osumi S, Yamaguchi S, Foster A.S, Spijker P, Meyer E. Kawai S, Saito S, Osumi S, Yamaguchi S, Foster A.S, Spijker P, Meyer E. Kawai S, Saito S, Osumi S, Yamaguchi S, Foster A.S, Spijker P, Meyer E. Atomically controlled substitutional boron-doping of graphene nanoribbons Atomically controlled substitutional boron-doping of graphene nanoribbons Atomically controlled substitutional boron-doping of graphene nanoribbons Nature Communications, 6 Nature Communications, 6 Nature Communications, 6 2015 Refereed Disclose to all
Glotzbach C, G{\"o}deke N, Fr{\"o}hlich R, Daniliuc C.-G, Saito S, Yamaguchi S, W{\"u}rthwein E.-U. Glotzbach C, G{\"o}deke N, Fr{\"o}hlich R, Daniliuc C.-G, Saito S, Yamaguchi S, W{\"u}rthwein E.-U. Glotzbach C, G{\"o}deke N, Fr{\"o}hlich R, Daniliuc C.-G, Saito S, Yamaguchi S, W{\"u}rthwein E.-U. Fluorescent benzene-centered mono-, bis- and tris-triazapentadiene-boron complexes Fluorescent benzene-centered mono-, bis- and tris-triazapentadiene-boron complexes Fluorescent benzene-centered mono-, bis- and tris-triazapentadiene-boron complexes Dalton Transactions, 44, 20, 9659-9671 Dalton Transactions, 44, 20, 9659-9671 Dalton Transactions, 44, 20, 9659-9671 2015 Refereed Disclose to all
Christoph Glotzbach, Nadine Gödeke, Roland Fröhlich, Constantin-Gabriel Daniliuc, Shohei Saito, Shigehiro Yamaguchi, Ernst-Ulrich Würthwein Christoph Glotzbach, Nadine Gödeke, Roland Fröhlich, Constantin-Gabriel Daniliuc, Shohei Saito, Shigehiro Yamaguchi, Ernst-Ulrich Würthwein Christoph Glotzbach, Nadine Gödeke, Roland Fröhlich, Constantin-Gabriel Daniliuc, Shohei Saito, Shigehiro Yamaguchi, Ernst-Ulrich Würthwein Fluorescent benzene-centered mono-, bis- and tris-triazapentadiene–boron complexes Fluorescent benzene-centered mono-, bis- and tris-triazapentadiene–boron complexes Fluorescent benzene-centered mono-, bis- and tris-triazapentadiene–boron complexes Dalton Trans., 44, 20, 9659 Dalton Trans., 44, 20, 9659 Dalton Trans., 44, 20, 9659 2015 Refereed Disclose to all
Chih-Ming Chou, Shunpei Nobusue, Shohei Saito, Daishi Inoue, Daisuke Hashizume, Shigehiro Yamaguchi Chih-Ming Chou, Shunpei Nobusue, Shohei Saito, Daishi Inoue, Daisuke Hashizume, Shigehiro Yamaguchi Chih-Ming Chou, Shunpei Nobusue, Shohei Saito, Daishi Inoue, Daisuke Hashizume, Shigehiro Yamaguchi Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Chem. Sci., 6, 4, 2354 Chem. Sci., 6, 4, 2354 Chem. Sci., 6, 4, 2354 2015 Refereed Disclose to all
Chou C.-M, Nobusue S, Saito S, Inoue D, Hashizume D, Yamaguchi S. Chou C.-M, Nobusue S, Saito S, Inoue D, Hashizume D, Yamaguchi S. Chou C.-M, Nobusue S, Saito S, Inoue D, Hashizume D, Yamaguchi S. Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations Chemical Science, 6, 4, 2354-2359 Chemical Science, 6, 4, 2354-2359 Chemical Science, 6, 4, 2354-2359 2015 Refereed Disclose to all
Naoya Suzuki, Aiko Fukazawa, Kazuhiko Nagura, Shohei Saito, Hirotaka Kitoh-Nishioka, Daisuke Yokogawa, Stephan Irle, Shigehiro Yamaguchi Naoya Suzuki, Aiko Fukazawa, Kazuhiko Nagura, Shohei Saito, Hirotaka Kitoh-Nishioka, Daisuke Yokogawa, Stephan Irle, Shigehiro Yamaguchi Naoya Suzuki, Aiko Fukazawa, Kazuhiko Nagura, Shohei Saito, Hirotaka Kitoh-Nishioka, Daisuke Yokogawa, Stephan Irle, Shigehiro Yamaguchi A Strap Strategy for Construction of an Excited-State Intramolecular Proton Transfer (ESIPT) System with Dual Fluorescence A Strap Strategy for Construction of an Excited-State Intramolecular Proton Transfer (ESIPT) System with Dual Fluorescence A Strap Strategy for Construction of an Excited-State Intramolecular Proton Transfer (ESIPT) System with Dual Fluorescence Angew. Chem., 126, 31, 8370 Angew. Chem., 126, 31, 8370 Angew. Chem., 126, 31, 8370 2014/06 Refereed Disclose to all
Chunxue Yuan, Shohei Saito, Cristopher Camacho, Tim Kowalczyk, Stephan Irle, Shigehiro Yamaguchi Chunxue Yuan, Shohei Saito, Cristopher Camacho, Tim Kowalczyk, Stephan Irle, Shigehiro Yamaguchi Chunxue Yuan, Shohei Saito, Cristopher Camacho, Tim Kowalczyk, Stephan Irle, Shigehiro Yamaguchi Inside Cover: Hybridization of a Flexible Cyclooctatetraene Core and Rigid Aceneimide Wings for Multiluminescent Flapping π Systems (Chem. Eur. J. 8/2014) Inside Cover: Hybridization of a Flexible Cyclooctatetraene Core and Rigid Aceneimide Wings for Multiluminescent Flapping π Systems (Chem. Eur. J. 8/2014) Inside Cover: Hybridization of a Flexible Cyclooctatetraene Core and Rigid Aceneimide Wings for Multiluminescent Flapping π Systems (Chem. Eur. J. 8/2014) Chem. Eur. J., 20, 8, 2086 Chem. Eur. J., 20, 8, 2086 Chem. Eur. J., 20, 8, 2086 2014/02 Refereed Disclose to all
C. Yuan, S. Saito, C. Camacho, T. Kowaiczyk, S. Irle, and S. Yamaguchi C. Yuan, S. Saito, C. Camacho, T. Kowaiczyk, S. Irle, and S. Yamaguchi C. Yuan, S. Saito, C. Camacho, T. Kowaiczyk, S. Irle, and S. Yamaguchi Hybridization of a Flexible Cyclooctatetraene Core and Rigid Aceneimide Wings for Multi-Luminescent Flapping pi Systems Hybridization of a Flexible Cyclooctatetraene Core and Rigid Aceneimide Wings for Multi-Luminescent Flapping pi Systems Hybridization of a Flexible Cyclooctatetraene Core and Rigid Aceneimide Wings for Multi-Luminescent Flapping pi Systems Chem. Eur. J., 20, 8, 2193-2200 Chem. Eur. J., 20, 8, 2193-2200 Chem. Eur. J., 20, 8, 2193-2200 2014 Refereed Disclose to all
Suzuki N, Fukazawa A, Nagura K, Saito S, Kitoh-Nishioka H, Yokogawa D, Irle S, Yamaguchi S. Suzuki N, Fukazawa A, Nagura K, Saito S, Kitoh-Nishioka H, Yokogawa D, Irle S, Yamaguchi S. Suzuki N, Fukazawa A, Nagura K, Saito S, Kitoh-Nishioka H, Yokogawa D, Irle S, Yamaguchi S. A strap strategy for construction of an excited-state intramolecular proton transfer (ESIPT) system with dual fluorescence A strap strategy for construction of an excited-state intramolecular proton transfer (ESIPT) system with dual fluorescence A strap strategy for construction of an excited-state intramolecular proton transfer (ESIPT) system with dual fluorescence Angewandte Chemie - International Edition, 53, 31, 8231-8235 Angewandte Chemie - International Edition, 53, 31, 8231-8235 Angewandte Chemie - International Edition, 53, 31, 8231-8235 2014 Refereed Disclose to all
Chou C.-M, Saito S, Yamaguchi S. Chou C.-M, Saito S, Yamaguchi S. Chou C.-M, Saito S, Yamaguchi S. Heterotriangulenes π-expanded at bridging positions Heterotriangulenes π-expanded at bridging positions Heterotriangulenes π-expanded at bridging positions Organic Letters, 16, 11, 2868-2871 Organic Letters, 16, 11, 2868-2871 Organic Letters, 16, 11, 2868-2871 2014 Refereed Disclose to all
Matsuo K, Saito S, Yamaguchi S. Matsuo K, Saito S, Yamaguchi S. Matsuo K, Saito S, Yamaguchi S. Photodissociation of B-N Lewis adducts: A partially fused trinaphthylborane with dual fluorescence Photodissociation of B-N Lewis adducts: A partially fused trinaphthylborane with dual fluorescence Photodissociation of B-N Lewis adducts: A partially fused trinaphthylborane with dual fluorescence Journal of the American Chemical Society, 136, 36, 12580-12583 Journal of the American Chemical Society, 136, 36, 12580-12583 Journal of the American Chemical Society, 136, 36, 12580-12583 2014 Refereed Disclose to all
K. Nagura, S. Saito, H. Yusa, H. Yamawaki, H. Fujihisa, H. Sato, Y. Shimoikeda, and S. Yamaguchi K. Nagura, S. Saito, H. Yusa, H. Yamawaki, H. Fujihisa, H. Sato, Y. Shimoikeda, and S. Yamaguchi K. Nagura, S. Saito, H. Yusa, H. Yamawaki, H. Fujihisa, H. Sato, Y. Shimoikeda, and S. Yamaguchi Distinct Responses to Mechanical Grinding and Hydrostatic Pressure in Luminescent Chromism of Tetrathiazolylthiophene Distinct Responses to Mechanical Grinding and Hydrostatic Pressure in Luminescent Chromism of Tetrathiazolylthiophene Distinct Responses to Mechanical Grinding and Hydrostatic Pressure in Luminescent Chromism of Tetrathiazolylthiophene J. Am. Chem. Soc., 135, 28, 10322-10325 J. Am. Chem. Soc., 135, 28, 10322-10325 J. Am. Chem. Soc., 135, 28, 10322-10325 2013 Refereed Disclose to all
C. Yuan, S. Saito, C. Camacho, S. Irle, I. Hisaki, and S. Yamaguchi C. Yuan, S. Saito, C. Camacho, S. Irle, I. Hisaki, and S. Yamaguchi C. Yuan, S. Saito, C. Camacho, S. Irle, I. Hisaki, and S. Yamaguchi A π-Conjugated System with Flexibility and Rigidity that Shows Environment-Dependent RGB Luminescence A π-Conjugated System with Flexibility and Rigidity that Shows Environment-Dependent RGB Luminescence A π-Conjugated System with Flexibility and Rigidity that Shows Environment-Dependent RGB Luminescence J. Am. Chem. Soc., 135, 24, 8842-8845 J. Am. Chem. Soc., 135, 24, 8842-8845 J. Am. Chem. Soc., 135, 24, 8842-8845 2013 Refereed Disclose to all
Dou C, Saito S, Yamaguchi S. Dou C, Saito S, Yamaguchi S. Dou C, Saito S, Yamaguchi S. A pentacoordinate boron-containing π-electron system with Cl-B-Cl three-center four-electron bonds A pentacoordinate boron-containing π-electron system with Cl-B-Cl three-center four-electron bonds A pentacoordinate boron-containing π-electron system with Cl-B-Cl three-center four-electron bonds Journal of the American Chemical Society, 135, 25, 9346-9349 Journal of the American Chemical Society, 135, 25, 9346-9349 Journal of the American Chemical Society, 135, 25, 9346-9349 2013 Refereed Disclose to all
Iida A, Saito S, Sasamori T, Yamaguchi S. Iida A, Saito S, Sasamori T, Yamaguchi S. Iida A, Saito S, Sasamori T, Yamaguchi S. Borylated dibenzoborepin: Synthesis by skeletal rearrangement and photochromism based on bora-Nazarov cyclization Borylated dibenzoborepin: Synthesis by skeletal rearrangement and photochromism based on bora-Nazarov cyclization Borylated dibenzoborepin: Synthesis by skeletal rearrangement and photochromism based on bora-Nazarov cyclization Angewandte Chemie - International Edition, 52, 13, 3760-3764 Angewandte Chemie - International Edition, 52, 13, 3760-3764 Angewandte Chemie - International Edition, 52, 13, 3760-3764 2013 Refereed Disclose to all
Glotzbach C, Kauscher U, Voskuhl J, Kehr N.S, Stuart M.C.A, Fr{\"o}hlich R, Galla H.J, Ravoo B.J, Nagura K, Saito S, Yamaguchi S, W{\"u}rthwein E.-U. Glotzbach C, Kauscher U, Voskuhl J, Kehr N.S, Stuart M.C.A, Fr{\"o}hlich R, Galla H.J, Ravoo B.J, Nagura K, Saito S, Yamaguchi S, W{\"u}rthwein E.-U. Glotzbach C, Kauscher U, Voskuhl J, Kehr N.S, Stuart M.C.A, Fr{\"o}hlich R, Galla H.J, Ravoo B.J, Nagura K, Saito S, Yamaguchi S, W{\"u}rthwein E.-U. Fluorescent modular boron systems based on NNN- and ONO-tridentate ligands: Self-assembly and cell imaging Fluorescent modular boron systems based on NNN- and ONO-tridentate ligands: Self-assembly and cell imaging Fluorescent modular boron systems based on NNN- and ONO-tridentate ligands: Self-assembly and cell imaging Journal of Organic Chemistry, 78, 9, 4410-4418 Journal of Organic Chemistry, 78, 9, 4410-4418 Journal of Organic Chemistry, 78, 9, 4410-4418 2013 Refereed Disclose to all
Fukazawa A, Adachi M, Nakakura K, Saito S, Yamaguchi S. Fukazawa A, Adachi M, Nakakura K, Saito S, Yamaguchi S. Fukazawa A, Adachi M, Nakakura K, Saito S, Yamaguchi S. S-Pechmann dye: A thiolactone-containing organic dye with a pronounced electron-accepting character and its solid-state photophysical properties S-Pechmann dye: A thiolactone-containing organic dye with a pronounced electron-accepting character and its solid-state photophysical properties S-Pechmann dye: A thiolactone-containing organic dye with a pronounced electron-accepting character and its solid-state photophysical properties Chemical Communications, 49, 64, 7117-7119 Chemical Communications, 49, 64, 7117-7119 Chemical Communications, 49, 64, 7117-7119 2013 Refereed Disclose to all
Dou C, Saito S, Gao L, Matsumoto N, Karasawa T, Zhang H, Fukazawa A, Yamaguchi S. Dou C, Saito S, Gao L, Matsumoto N, Karasawa T, Zhang H, Fukazawa A, Yamaguchi S. Dou C, Saito S, Gao L, Matsumoto N, Karasawa T, Zhang H, Fukazawa A, Yamaguchi S. Sequential electrophilic and photochemical cyclizations from bis(bithienyl)acetylene to a tetrathienonaphthalene core Sequential electrophilic and photochemical cyclizations from bis(bithienyl)acetylene to a tetrathienonaphthalene core Sequential electrophilic and photochemical cyclizations from bis(bithienyl)acetylene to a tetrathienonaphthalene core Organic Letters, 15, 1, 80-83 Organic Letters, 15, 1, 80-83 Organic Letters, 15, 1, 80-83 2013 Refereed Disclose to all
Mouri K, Saito S, Hisaki I, Yamaguchi S. Mouri K, Saito S, Hisaki I, Yamaguchi S. Mouri K, Saito S, Hisaki I, Yamaguchi S. Thermal 8π electrocyclic reaction of heteroarene tetramers: New efficient access to π-extended cyclooctatetraenes Thermal 8π electrocyclic reaction of heteroarene tetramers: New efficient access to π-extended cyclooctatetraenes Thermal 8π electrocyclic reaction of heteroarene tetramers: New efficient access to π-extended cyclooctatetraenes Chemical Science, 4, 12, 4465-4469 Chemical Science, 4, 12, 4465-4469 Chemical Science, 4, 12, 4465-4469 2013 Refereed Disclose to all
C. Dou, S. Saito, K. Matsuo, I. Hisaki, and S. Yamaguchi C. Dou, S. Saito, K. Matsuo, I. Hisaki, and S. Yamaguchi C. Dou, S. Saito, K. Matsuo, I. Hisaki, and S. Yamaguchi Boron-Containing PAH as a Substructure of Boron-Doped Graphene Boron-Containing PAH as a Substructure of Boron-Doped Graphene Boron-Containing PAH as a Substructure of Boron-Doped Graphene Angew. Chem. Int. Ed., 51, 49, 12206-12210 Angew. Chem. Int. Ed., 51, 49, 12206-12210 Angew. Chem. Int. Ed., 51, 49, 12206-12210 2012 Refereed Disclose to all
S. Saito, K. Matsuo, and S. Yamaguchi S. Saito, K. Matsuo, and S. Yamaguchi S. Saito, K. Matsuo, and S. Yamaguchi Polycyclic pi-Electron System with Boron at Its Center Polycyclic pi-Electron System with Boron at Its Center Polycyclic pi-Electron System with Boron at Its Center J. Am. Chem. Soc., 134, 22, 9130-9133 J. Am. Chem. Soc., 134, 22, 9130-9133 J. Am. Chem. Soc., 134, 22, 9130-9133 2012 Refereed Disclose to all
Hayashi Y, Obata N, Tamaru M, Yamaguchi S, Matsuo Y, Saeki A, Seki S, Kureishi Y, Saito S, Yamaguchi S, Shinokubo H. Hayashi Y, Obata N, Tamaru M, Yamaguchi S, Matsuo Y, Saeki A, Seki S, Kureishi Y, Saito S, Yamaguchi S, Shinokubo H. Hayashi Y, Obata N, Tamaru M, Yamaguchi S, Matsuo Y, Saeki A, Seki S, Kureishi Y, Saito S, Yamaguchi S, Shinokubo H. Facile synthesis of biphenyl-fused BODIPY and its property Facile synthesis of biphenyl-fused BODIPY and its property Facile synthesis of biphenyl-fused BODIPY and its property Organic Letters, 14, 3, 866-869 Organic Letters, 14, 3, 866-869 Organic Letters, 14, 3, 866-869 2012 Refereed Disclose to all
Mouri K, Saito S, Yamaguchi S. Mouri K, Saito S, Yamaguchi S. Mouri K, Saito S, Yamaguchi S. Highly flexible π-expanded cyclooctatetraenes: Cyclic thiazole tetramers with head-to-tail connection Highly flexible π-expanded cyclooctatetraenes: Cyclic thiazole tetramers with head-to-tail connection Highly flexible π-expanded cyclooctatetraenes: Cyclic thiazole tetramers with head-to-tail connection Angewandte Chemie - International Edition, 51, 24, 5971-5975 Angewandte Chemie - International Edition, 51, 24, 5971-5975 Angewandte Chemie - International Edition, 51, 24, 5971-5975 2012 Refereed Disclose to all
Saito S, Nakakura K, Yamaguchi S. Saito S, Nakakura K, Yamaguchi S. Saito S, Nakakura K, Yamaguchi S. Macrocyclic restriction with flexible alkylene linkers: A simple strategy to control the solid-state properties of π-conjugated systems Macrocyclic restriction with flexible alkylene linkers: A simple strategy to control the solid-state properties of π-conjugated systems Macrocyclic restriction with flexible alkylene linkers: A simple strategy to control the solid-state properties of π-conjugated systems Angewandte Chemie - International Edition, 51, 3, 714-717 Angewandte Chemie - International Edition, 51, 3, 714-717 Angewandte Chemie - International Edition, 51, 3, 714-717 2012 Refereed Disclose to all
Nagura K, Saito S, Fr{\"o}hlich R, Glorius F, Yamaguchi S. Nagura K, Saito S, Fr{\"o}hlich R, Glorius F, Yamaguchi S. Nagura K, Saito S, Fr{\"o}hlich R, Glorius F, Yamaguchi S. N-heterocyclic carbene boranes as electron-donating and electron-accepting components of π-conjugated systems N-heterocyclic carbene boranes as electron-donating and electron-accepting components of π-conjugated systems N-heterocyclic carbene boranes as electron-donating and electron-accepting components of π-conjugated systems Angewandte Chemie - International Edition, 51, 31, 7762-7766 Angewandte Chemie - International Edition, 51, 31, 7762-7766 Angewandte Chemie - International Edition, 51, 31, 7762-7766 2012 Refereed Disclose to all
Moriya K, Yoneda T, Saito S, Osuka A. Moriya K, Yoneda T, Saito S, Osuka A. Moriya K, Yoneda T, Saito S, Osuka A. A Möbius aromatic Pd(I10) complex of [28]hexaphyrin(2.1.1.0.1.1) A Möbius aromatic Pd(I10) complex of [28]hexaphyrin(2.1.1.0.1.1) A Möbius aromatic Pd(I10) complex of [28]hexaphyrin(2.1.1.0.1.1) Chemistry Letters, 40, 5, 455-457 Chemistry Letters, 40, 5, 455-457 Chemistry Letters, 40, 5, 455-457 2011 Refereed Disclose to all
Osuka A, Saito S. Osuka A, Saito S. Osuka A, Saito S. Expanded porphyrins and aromaticity Expanded porphyrins and aromaticity Expanded porphyrins and aromaticity Chemical Communications, 47, 15, 4330-4339 Chemical Communications, 47, 15, 4330-4339 Chemical Communications, 47, 15, 4330-4339 2011 Refereed Disclose to all
Saito S, Osuka A. Saito S, Osuka A. Saito S, Osuka A. Expanded porphyrins: Intriguing structures, electronic properties, and reactivities Expanded porphyrins: Intriguing structures, electronic properties, and reactivities Expanded porphyrins: Intriguing structures, electronic properties, and reactivities Angewandte Chemie - International Edition, 50, 19, 4342-4373 Angewandte Chemie - International Edition, 50, 19, 4342-4373 Angewandte Chemie - International Edition, 50, 19, 4342-4373 2011 Refereed Disclose to all
Yoneda T, Saito S, Yorimitsu H, Osuka A. Yoneda T, Saito S, Yorimitsu H, Osuka A. Yoneda T, Saito S, Yorimitsu H, Osuka A. Palladium(II)-triggered rearrangement of heptaphyrins to N-confused porphyrins Palladium(II)-triggered rearrangement of heptaphyrins to N-confused porphyrins Palladium(II)-triggered rearrangement of heptaphyrins to N-confused porphyrins Angewandte Chemie - International Edition, 50, 15, 3475-3478 Angewandte Chemie - International Edition, 50, 15, 3475-3478 Angewandte Chemie - International Edition, 50, 15, 3475-3478 2011 Refereed Disclose to all
Yoon M.-C, Kim P, Yoo H, Shimizu S, Koide T, Tokuji S, Saito S, Osuka A, Kim D. Yoon M.-C, Kim P, Yoo H, Shimizu S, Koide T, Tokuji S, Saito S, Osuka A, Kim D. Yoon M.-C, Kim P, Yoo H, Shimizu S, Koide T, Tokuji S, Saito S, Osuka A, Kim D. Solvent- and temperature-dependent conformational changes between hückel antiaromatic and möbius aromatic species in meso-trifluoromethyl substituted [28]hexaphyrins Solvent- and temperature-dependent conformational changes between hückel antiaromatic and möbius aromatic species in meso-trifluoromethyl substituted [28]hexaphyrins Solvent- and temperature-dependent conformational changes between hückel antiaromatic and möbius aromatic species in meso-trifluoromethyl substituted [28]hexaphyrins Journal of Physical Chemistry B, 115, 50, 14928-14937 Journal of Physical Chemistry B, 115, 50, 14928-14937 Journal of Physical Chemistry B, 115, 50, 14928-14937 2011 Refereed Disclose to all
Yoon M.-C, Shin J.-Y, Lim J.M, Saito S, Yoneda T, Osuka A, Kim D. Yoon M.-C, Shin J.-Y, Lim J.M, Saito S, Yoneda T, Osuka A, Kim D. Yoon M.-C, Shin J.-Y, Lim J.M, Saito S, Yoneda T, Osuka A, Kim D. Solvent-dependent aromatic versus antiaromatic conformational switching in meso-(heptakis)pentafluorophenyl [32]heptaphyrin Solvent-dependent aromatic versus antiaromatic conformational switching in meso-(heptakis)pentafluorophenyl [32]heptaphyrin Solvent-dependent aromatic versus antiaromatic conformational switching in meso-(heptakis)pentafluorophenyl [32]heptaphyrin Chemistry - A European Journal, 17, 24, 6707-6715 Chemistry - A European Journal, 17, 24, 6707-6715 Chemistry - A European Journal, 17, 24, 6707-6715 2011 Refereed Disclose to all
Moriya K, Saito S, Osuka A. Moriya K, Saito S, Osuka A. Moriya K, Saito S, Osuka A. Boron(III) induced skeletal rearrangement of hexaphyrin(1.1.1.1.1.1) to hexaphyrin(2.1.1.0.1.1) Boron(III) induced skeletal rearrangement of hexaphyrin(1.1.1.1.1.1) to hexaphyrin(2.1.1.0.1.1) Boron(III) induced skeletal rearrangement of hexaphyrin(1.1.1.1.1.1) to hexaphyrin(2.1.1.0.1.1) Angewandte Chemie - International Edition, 49, 25, 4297-4300 Angewandte Chemie - International Edition, 49, 25, 4297-4300 Angewandte Chemie - International Edition, 49, 25, 4297-4300 2010 Refereed Disclose to all
Sakamoto R, Saito S, Shimizu S, Inokuma Y, Aratani N, Osuka A. Sakamoto R, Saito S, Shimizu S, Inokuma Y, Aratani N, Osuka A. Sakamoto R, Saito S, Shimizu S, Inokuma Y, Aratani N, Osuka A. Meso-trifluoromethyl-substituted subporphyrin from ring-splitting reaction of meso-trifluoromethyl-substituted [32]Heptaphyrin(1.1.1.1.1.1.1) Meso-trifluoromethyl-substituted subporphyrin from ring-splitting reaction of meso-trifluoromethyl-substituted [32]Heptaphyrin(1.1.1.1.1.1.1) Meso-trifluoromethyl-substituted subporphyrin from ring-splitting reaction of meso-trifluoromethyl-substituted [32]Heptaphyrin(1.1.1.1.1.1.1) Chemistry Letters, 39, 5, 439-441 Chemistry Letters, 39, 5, 439-441 Chemistry Letters, 39, 5, 439-441 2010 Refereed Disclose to all
Tanaka T, Sugita T, Tokuji S, Saito S, Osuka A. Tanaka T, Sugita T, Tokuji S, Saito S, Osuka A. Tanaka T, Sugita T, Tokuji S, Saito S, Osuka A. Metal complexes of chiral Möbius aromatic [28]hexaphyrin(1.1.1.1.1.1): Enantiomeric separation, absolute stereochemistry, and asymmetric synthesis Metal complexes of chiral Möbius aromatic [28]hexaphyrin(1.1.1.1.1.1): Enantiomeric separation, absolute stereochemistry, and asymmetric synthesis Metal complexes of chiral Möbius aromatic [28]hexaphyrin(1.1.1.1.1.1): Enantiomeric separation, absolute stereochemistry, and asymmetric synthesis Angewandte Chemie - International Edition, 49, 37, 6619-6621 Angewandte Chemie - International Edition, 49, 37, 6619-6621 Angewandte Chemie - International Edition, 49, 37, 6619-6621 2010 Refereed Disclose to all
Higashino T, Lim J.M, Miura T, Saito S, Shin J.-Y, Kim D, Osuka A. Higashino T, Lim J.M, Miura T, Saito S, Shin J.-Y, Kim D, Osuka A. Higashino T, Lim J.M, Miura T, Saito S, Shin J.-Y, Kim D, Osuka A. Möbius antiaromatic bisphosphorus complexes of [30]hexaphyrins Möbius antiaromatic bisphosphorus complexes of [30]hexaphyrins Möbius antiaromatic bisphosphorus complexes of [30]hexaphyrins Angewandte Chemie - International Edition, 49, 29, 4950-4954 Angewandte Chemie - International Edition, 49, 29, 4950-4954 Angewandte Chemie - International Edition, 49, 29, 4950-4954 2010 Refereed Disclose to all
Miura T, Higashino T, Saito S, Osuka A. Miura T, Higashino T, Saito S, Osuka A. Miura T, Higashino T, Saito S, Osuka A. Phosphorus complexes of the first expanded isophlorins Phosphorus complexes of the first expanded isophlorins Phosphorus complexes of the first expanded isophlorins Chemistry - A European Journal, 16, 1, 55-59 Chemistry - A European Journal, 16, 1, 55-59 Chemistry - A European Journal, 16, 1, 55-59 2010 Refereed Disclose to all
Lim J.M, Shin J.-Y, Tanaka Y, Saito S, Osuka A, Kim D. Lim J.M, Shin J.-Y, Tanaka Y, Saito S, Osuka A, Kim D. Lim J.M, Shin J.-Y, Tanaka Y, Saito S, Osuka A, Kim D. Protonated [4n] and [4n+2]π octaphyrins choose their möbius/hückel aromatic topology Protonated [4n] and [4n+2]π octaphyrins choose their möbius/hückel aromatic topology Protonated [4n] and [4n+2]π octaphyrins choose their möbius/hückel aromatic topology Journal of the American Chemical Society, 132, 9, 3105-3114 Journal of the American Chemical Society, 132, 9, 3105-3114 Journal of the American Chemical Society, 132, 9, 3105-3114 2010 Refereed Disclose to all
Tokuji S, Shin J.-Y, Kil S.K, Jong M.L, Youfu K, Saito S, Kim D, Osuka A. Tokuji S, Shin J.-Y, Kil S.K, Jong M.L, Youfu K, Saito S, Kim D, Osuka A. Tokuji S, Shin J.-Y, Kil S.K, Jong M.L, Youfu K, Saito S, Kim D, Osuka A. Facile formation of a benzopyrane-fused [28]hexaphyrin that exhibits distinct Möbius aromaticity Facile formation of a benzopyrane-fused [28]hexaphyrin that exhibits distinct Möbius aromaticity Facile formation of a benzopyrane-fused [28]hexaphyrin that exhibits distinct Möbius aromaticity Journal of the American Chemical Society, 131, 21, 7240-7241 Journal of the American Chemical Society, 131, 21, 7240-7241 Journal of the American Chemical Society, 131, 21, 7240-7241 2009 Refereed Disclose to all
Koide T, Youfu K, Saito S, Osuka A. Koide T, Youfu K, Saito S, Osuka A. Koide T, Youfu K, Saito S, Osuka A. Multiple conformational changes of β-tetraphenyl meso- hexakis(pentafluorophenyl) substituted [26] and [28]hexaphyrins(1.1.1.1.1.1) Multiple conformational changes of β-tetraphenyl meso- hexakis(pentafluorophenyl) substituted [26] and [28]hexaphyrins(1.1.1.1.1.1) Multiple conformational changes of β-tetraphenyl meso- hexakis(pentafluorophenyl) substituted [26] and [28]hexaphyrins(1.1.1.1.1.1) Chemical Communications, 40, 6047-6049 Chemical Communications, 40, 6047-6049 Chemical Communications, 40, 6047-6049 2009 Refereed Disclose to all
Saito S, Furukawa K, Osuka A. Saito S, Furukawa K, Osuka A. Saito S, Furukawa K, Osuka A. T-shaped three-coordinate copper(II) heptaphyrin complexes T-shaped three-coordinate copper(II) heptaphyrin complexes T-shaped three-coordinate copper(II) heptaphyrin complexes Angewandte Chemie - International Edition, 48, 43, 8086-8089 Angewandte Chemie - International Edition, 48, 43, 8086-8089 Angewandte Chemie - International Edition, 48, 43, 8086-8089 2009 Refereed Disclose to all
Kim S, Yoon S, Ricks B, Shin Y, Mori S, Sankar J, Saito S, Jung Y.M, Wasielewski M.R, Osuka A, Kim D. Kim S, Yoon S, Ricks B, Shin Y, Mori S, Sankar J, Saito S, Jung Y.M, Wasielewski M.R, Osuka A, Kim D. Kim S, Yoon S, Ricks B, Shin Y, Mori S, Sankar J, Saito S, Jung Y.M, Wasielewski M.R, Osuka A, Kim D. Temperature-dependent conformational change of weso- Hexakis(pentafluorophenyl) [28]Hexaphyrins(1.1.1.1.1.1) into mobius structures Temperature-dependent conformational change of weso- Hexakis(pentafluorophenyl) [28]Hexaphyrins(1.1.1.1.1.1) into mobius structures Temperature-dependent conformational change of weso- Hexakis(pentafluorophenyl) [28]Hexaphyrins(1.1.1.1.1.1) into mobius structures Journal of Physical Chemistry A, 113, 16, 4498-4506 Journal of Physical Chemistry A, 113, 16, 4498-4506 Journal of Physical Chemistry A, 113, 16, 4498-4506 2009 Refereed Disclose to all
Xie Y.-S, Yamaguchi K, Toganoh M, Uno H, Suzuki M, Mori S, Saito S, Osuka A, Furuta H. Xie Y.-S, Yamaguchi K, Toganoh M, Uno H, Suzuki M, Mori S, Saito S, Osuka A, Furuta H. Xie Y.-S, Yamaguchi K, Toganoh M, Uno H, Suzuki M, Mori S, Saito S, Osuka A, Furuta H. Triply N-confused hexaphyrins: Near-infrared luminescent dyes with a triangular shape Triply N-confused hexaphyrins: Near-infrared luminescent dyes with a triangular shape Triply N-confused hexaphyrins: Near-infrared luminescent dyes with a triangular shape Angewandte Chemie - International Edition, 48, 30, 5496-5499 Angewandte Chemie - International Edition, 48, 30, 5496-5499 Angewandte Chemie - International Edition, 48, 30, 5496-5499 2009 Refereed Disclose to all
Tsurumaki E, Saito S, Kil S.K, Jong M.L, Inokuma Y, Kim D, Osuka A. Tsurumaki E, Saito S, Kil S.K, Jong M.L, Inokuma Y, Kim D, Osuka A. Tsurumaki E, Saito S, Kil S.K, Jong M.L, Inokuma Y, Kim D, Osuka A. Synthesis and characterization of meso-aryl-substituted subchlorins Synthesis and characterization of meso-aryl-substituted subchlorins Synthesis and characterization of meso-aryl-substituted subchlorins Journal of the American Chemical Society, 130, 2, 438-439 Journal of the American Chemical Society, 130, 2, 438-439 Journal of the American Chemical Society, 130, 2, 438-439 2008 Refereed Disclose to all
Sankar J, Mori S, Saito S, Rath H, Suzuki M, Inokuma Y, Shinokubo H, Kil S.K, Zin S.Y, Shin J.-Y, Jong M.L, Matsuzaki Y, Matsushita O, Muranaka A, Kobayashi N, Kim D, Osuka A. Sankar J, Mori S, Saito S, Rath H, Suzuki M, Inokuma Y, Shinokubo H, Kil S.K, Zin S.Y, Shin J.-Y, Jong M.L, Matsuzaki Y, Matsushita O, Muranaka A, Kobayashi N, Kim D, Osuka A. Sankar J, Mori S, Saito S, Rath H, Suzuki M, Inokuma Y, Shinokubo H, Kil S.K, Zin S.Y, Shin J.-Y, Jong M.L, Matsuzaki Y, Matsushita O, Muranaka A, Kobayashi N, Kim D, Osuka A. Unambiguous identification of Möbius aromaticity for meso-aryl-substituted [28]hexaphyrins(1.1.1.1.1.1) Unambiguous identification of Möbius aromaticity for meso-aryl-substituted [28]hexaphyrins(1.1.1.1.1.1) Unambiguous identification of Möbius aromaticity for meso-aryl-substituted [28]hexaphyrins(1.1.1.1.1.1) Journal of the American Chemical Society, 130, 41, 13568-13579 Journal of the American Chemical Society, 130, 41, 13568-13579 Journal of the American Chemical Society, 130, 41, 13568-13579 2008 Refereed Disclose to all
Tanaka Y, Saito S, Mori S, Aratani N, Shinokubo H, Shibata N, Higuchi Y, Yoon Z.S, Kim K.S, Noh S.B, Park J.K, Kim D, Osuka A. Tanaka Y, Saito S, Mori S, Aratani N, Shinokubo H, Shibata N, Higuchi Y, Yoon Z.S, Kim K.S, Noh S.B, Park J.K, Kim D, Osuka A. Tanaka Y, Saito S, Mori S, Aratani N, Shinokubo H, Shibata N, Higuchi Y, Yoon Z.S, Kim K.S, Noh S.B, Park J.K, Kim D, Osuka A. Metalation of expanded porphyrins: A chemical trigger used to produce molecular twisting and Möbius aromaticity Metalation of expanded porphyrins: A chemical trigger used to produce molecular twisting and Möbius aromaticity Metalation of expanded porphyrins: A chemical trigger used to produce molecular twisting and Möbius aromaticity Angewandte Chemie - International Edition, 47, 4, 681-684 Angewandte Chemie - International Edition, 47, 4, 681-684 Angewandte Chemie - International Edition, 47, 4, 681-684 2008 Refereed Disclose to all
Saito S, Shin J.-Y, Lim J.M, Kim K.S, Kim D, Osuka A. Saito S, Shin J.-Y, Lim J.M, Kim K.S, Kim D, Osuka A. Saito S, Shin J.-Y, Lim J.M, Kim K.S, Kim D, Osuka A. Protonation-triggered conformational changes to Möbius aromatic [32]heptaphyrins(1.1.1.1.1.1.1) Protonation-triggered conformational changes to Möbius aromatic [32]heptaphyrins(1.1.1.1.1.1.1) Protonation-triggered conformational changes to Möbius aromatic [32]heptaphyrins(1.1.1.1.1.1.1) Angewandte Chemie - International Edition, 47, 50, 9657-9660 Angewandte Chemie - International Edition, 47, 50, 9657-9660 Angewandte Chemie - International Edition, 47, 50, 9657-9660 2008 Refereed Disclose to all
Saito S, Kim K.S, Yoon Z.S, Kim D, Osuka A. Saito S, Kim K.S, Yoon Z.S, Kim D, Osuka A. Saito S, Kim K.S, Yoon Z.S, Kim D, Osuka A. Extrusion of boron(III) subporphyrin from meso-heptakis(pentafluorophenyl) [32]heptaphyrin upon cooperative CuII and BIII metalation Extrusion of boron(III) subporphyrin from meso-heptakis(pentafluorophenyl) [32]heptaphyrin upon cooperative CuII and BIII metalation Extrusion of boron(III) subporphyrin from meso-heptakis(pentafluorophenyl) [32]heptaphyrin upon cooperative CuII and BIII metalation Angewandte Chemie - International Edition, 46, 29, 5591-5593 Angewandte Chemie - International Edition, 46, 29, 5591-5593 Angewandte Chemie - International Edition, 46, 29, 5591-5593 2007 Refereed Disclose to all
Saito S, Osuka A. Saito S, Osuka A. Saito S, Osuka A. N-fusion reaction sequence of heptaphyrin(1.1.1.1.1.1.1): Singly, doubly, and quadruply N-fused heptaphyrins N-fusion reaction sequence of heptaphyrin(1.1.1.1.1.1.1): Singly, doubly, and quadruply N-fused heptaphyrins N-fusion reaction sequence of heptaphyrin(1.1.1.1.1.1.1): Singly, doubly, and quadruply N-fused heptaphyrins Chemistry - A European Journal, 12, 35, 9095-9102 Chemistry - A European Journal, 12, 35, 9095-9102 Chemistry - A European Journal, 12, 35, 9095-9102 2006 Refereed Disclose to all
Anand V.G, Saito S, Shimizu S, Osuka A. Anand V.G, Saito S, Shimizu S, Osuka A. Anand V.G, Saito S, Shimizu S, Osuka A. Internally 1,4-phenylene-bridged meso aryl-substituted expanded porphyrins: The decaphyrin and octaphyrin cases Internally 1,4-phenylene-bridged meso aryl-substituted expanded porphyrins: The decaphyrin and octaphyrin cases Internally 1,4-phenylene-bridged meso aryl-substituted expanded porphyrins: The decaphyrin and octaphyrin cases Angewandte Chemie - International Edition, 44, 44, 7244-7248 Angewandte Chemie - International Edition, 44, 44, 7244-7248 Angewandte Chemie - International Edition, 44, 44, 7244-7248 2005 Refereed Disclose to all

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Title language:
Patents
Inventor(s) Inventor(s) (Japanese) Inventor(s) (English) Title Title(Japanese) Title(English) Stage Patent number Date Disclose
齊藤尚平、山口茂弘、小谷真央、渡辺 淳 齊藤尚平、山口茂弘、小谷真央、渡辺 淳 π共役化合物、π共役化合物を用いた接着剤、接着剤の使用方法、接合部の剥離方法、及びπ共役化合物の製造方法 π共役化合物、π共役化合物を用いた接着剤、接着剤の使用方法、接合部の剥離方法、及びπ共役化合物の製造方法 特許登録 特許第6284184号 2018/02 Disclose to all
Title language:
Awards
Title(Japanese) Title(English) Organization name(Japanese) Organization name(English) Date
日本液晶学会 論文賞(デバイス・応用分野) 日本液晶学会 JLCS 2018/09/05
第28回 田中ゴム科学技術賞 江野科学振興財団 Eno Foundation 2017/02/24
第9回 井上リサーチアウォード Inoue Research Award 井上科学振興財団 Inoue Foundation for Science 2017/02/03
第16回 光化学協会奨励賞 JPA Award for Young Scientists 光化学協会 JPA 2016/09/07
第6回 丸山記念研究奨励賞 The Maruyama Memorial Research Award 2015 丸山記念研究奨励賞 実行委員会 2015/04/11
平成26年度 文部科学大臣表彰 若手科学者賞 The Commendation for Science and Technology by the Minister of Education, Culture, Sports, Science and Technology, The Young Scientists’ Prize 文部科学省 Ministry of Education, Culture, Sports, Science and Technology - JAPAN 2014/04/15
第8回 PCCP Prize PCCP Prize 日本化学会 & 英国王立化学会 CSJ & RSC 2014/03/29
コニカミノルタ画像科学奨励賞 Konica Minolta Imaging Science Award コニカミノルタ Konica Minolta 2014/03/03
エヌエフ基金 研究開発奨励賞 エヌエフ基金 NF Foundation 2013/11/28
第2回 名古屋大学石田賞 石田財団 2013/11/08
有機合成化学協会 第23回 東ソー研究企画賞 有機合成化学協会 & 東ソー 2011/02/18
第27回 井上研究奨励賞 井上科学振興財団  Inoue Foundation for Science 2011/02/04
日本化学会 第64回 進歩賞 CSJ Award for Young Chemists 日本化学会 CSJ 2015/03/28

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External funds: competitive funds and Grants-in-Aid for Scientific Research (Kakenhi)
Type Position Title(Japanese) Title(English) Period
新学術領域研究(研究領域提案型) Representative 多分子協調場としてのフレキシブル光応答分子の機能集合システム構築 (平成28年度分) 2016/04/01-2017/03/31
若手研究(A) Representative 機能性可視化剤としての柔軟な発光分子の開発とマテリアルイメージング技術の確立 (平成28年度分) 2016/04/01-2017/03/31
新学術領域研究(研究領域提案型) Representative 多分子協調場としてのフレキシブル光応答分子の機能集合システム構築 (平成29年度分) 2017/04/01-2018/03/31
若手研究(A) Representative 機能性可視化剤としての柔軟な発光分子の開発とマテリアルイメージング技術の確立 (平成29年度分) 2017/04/01-2018/03/31
Teaching subject(s)
Name(Japanese) Name(English) Term Department Period
化学課題研究15 Special study course II (Chemistry) 15 通年 理学部 2016/04-2017/03
基礎有機化学II Basic Organic Chemistry II 後期 全学共通科目 2016/04-2017/03
有機化学ゼミナールIIIA Seminar on Organic Chemistry IIIA 前期 理学研究科 2016/04-2017/03
有機化学ゼミナールIIIB Seminar on Organic Chemistry IIIB 後期 理学研究科 2016/04-2017/03
有機化学ゼミナールIIIC Seminar on Organic Chemistry IIIC 前期 理学研究科 2016/04-2017/03
有機化学ゼミナールIIID Seminar on Organic Chemistry IIID 後期 理学研究科 2016/04-2017/03
有機化学演習IIIA Advanced Organic Chemistry IIIA 前期 理学研究科 2016/04-2017/03
有機化学演習IIIB Advanced Organic Chemistry IIIB 後期 理学研究科 2016/04-2017/03
有機化学演習IIIC Advanced Organic Chemistry IIIC 前期 理学研究科 2016/04-2017/03
有機化学演習IIID Advanced Organic Chemistry IIID 後期 理学研究科 2016/04-2017/03
現代有機化学論 Topics in Current Organic Chemistry 後期 理学研究科 2016/04-2017/03
集合有機化学論 Chemistry of Assembled Organic Compounds 後期 理学研究科 2016/04-2017/03
化学課題研究15 Special study course II (Chemistry) 15 通年 理学部 2017/04-2018/03
基礎有機化学I Basic Organic Chemistry I 前期 全学共通科目 2017/04-2018/03
基礎有機化学II Basic Organic Chemistry II 後期 全学共通科目 2017/04-2018/03
有機化学ゼミナールIIIA Seminar on Organic Chemistry IIIA 前期 理学研究科 2017/04-2018/03
有機化学ゼミナールIIIB Seminar on Organic Chemistry IIIB 後期 理学研究科 2017/04-2018/03
有機化学ゼミナールIIIC Seminar on Organic Chemistry IIIC 前期 理学研究科 2017/04-2018/03
有機化学ゼミナールIIID Seminar on Organic Chemistry IIID 後期 理学研究科 2017/04-2018/03
有機化学演習IIIA Advanced Organic Chemistry IIIA 前期 理学研究科 2017/04-2018/03
有機化学演習IIIB Advanced Organic Chemistry IIIB 後期 理学研究科 2017/04-2018/03
有機化学演習IIIC Advanced Organic Chemistry IIIC 前期 理学研究科 2017/04-2018/03
有機化学演習IIID Advanced Organic Chemistry IIID 後期 理学研究科 2017/04-2018/03
現代有機化学論 Topics in Current Organic Chemistry 後期 理学研究科 2017/04-2018/03
集合有機化学論 Chemistry of Assembled Organic Compounds 後期 理学研究科 2017/04-2018/03
化学課題研究15 Special study course II (Chemistry) 15 通年 理学部 2018/04-2019/03
基礎化学実験 Fundamental Chemical Experiments 後期 全学共通科目 2018/04-2019/03
基礎有機化学II Basic Organic Chemistry II 後期 全学共通科目 2018/04-2019/03
有機化学ゼミナールIIIA Seminar on Organic Chemistry IIIA 前期 理学研究科 2018/04-2019/03
有機化学ゼミナールIIIB Seminar on Organic Chemistry IIIB 後期 理学研究科 2018/04-2019/03
有機化学ゼミナールIIIC Seminar on Organic Chemistry IIIC 前期 理学研究科 2018/04-2019/03
有機化学ゼミナールIIID Seminar on Organic Chemistry IIID 後期 理学研究科 2018/04-2019/03
有機化学演習IIIA Advanced Organic Chemistry IIIA 前期 理学研究科 2018/04-2019/03
有機化学演習IIIB Advanced Organic Chemistry IIIB 後期 理学研究科 2018/04-2019/03
有機化学演習IIIC Advanced Organic Chemistry IIIC 前期 理学研究科 2018/04-2019/03
有機化学演習IIID Advanced Organic Chemistry IIID 後期 理学研究科 2018/04-2019/03
現代有機化学論 Topics in Current Organic Chemistry 後期 理学研究科 2018/04-2019/03
集合有機化学論 Chemistry of Assembled Organic Compounds 後期 理学研究科 2018/04-2019/03

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Faculty management (title, position)
Title Period
理学研究科環境・安全委員会委員 2017/04/01-2018/03/31
理学研究科環境・安全委員会委員 2018/04/01-2019/03/31