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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |
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 |
有 |
|
|
公開 |