Expanded porphyrins: intriguing structures, electronic properties, and reactivities S Saito, A Osuka Angewandte Chemie International Edition 50 (19), 4342-4373, 2011 | 623 | 2011 |
Atomically controlled substitutional boron-doping of graphene nanoribbons S Kawai, S Saito, S Osumi, S Yamaguchi, AS Foster, P Spijker, E Meyer Nature communications 6 (1), 8098, 2015 | 467 | 2015 |
Distinct responses to mechanical grinding and hydrostatic pressure in luminescent chromism of tetrathiazolylthiophene K Nagura, S Saito, H Yusa, H Yamawaki, H Fujihisa, H Sato, ... Journal of the American Chemical Society 135 (28), 10322-10325, 2013 | 467 | 2013 |
Metalation of expanded porphyrins: a chemical trigger used to produce molecular twisting and Mobius aromaticity Y Tanaka, S Saito, S Mori, N Aratani, H Shinokubo, N Shibata, Y Higuchi, ... ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH- 47 (4), 681, 2008 | 296 | 2008 |
Expanded porphyrins and aromaticity A Osuka, S Saito Chemical Communications 47 (15), 4330-4339, 2011 | 255 | 2011 |
Unambiguous Identification of Möbius Aromaticity for meso-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1) J Sankar, S Mori, S Saito, H Rath, M Suzuki, Y Inokuma, H Shinokubo, ... Journal of the American Chemical Society 130 (41), 13568-13579, 2008 | 236 | 2008 |
A boron‐containing PAH as a substructure of boron‐doped graphene C Dou, S Saito, K Matsuo, I Hisaki, S Yamaguchi Angewandte Chemie 124 (49), 12372-12376, 2012 | 229 | 2012 |
Polycyclic π-electron system with boron at its center S Saito, K Matsuo, S Yamaguchi Journal of the American Chemical Society 134 (22), 9130-9133, 2012 | 209 | 2012 |
A π-conjugated system with flexibility and rigidity that shows environment-dependent RGB luminescence C Yuan, S Saito, C Camacho, S Irle, I Hisaki, S Yamaguchi Journal of the American Chemical Society 135 (24), 8842-8845, 2013 | 197 | 2013 |
Expandierte Porphyrine: überraschende Strukturen, elektronische Eigenschaften und Reaktivitäten S Saito, A Osuka Angewandte Chemie 123 (19), 4432-4464, 2011 | 174 | 2011 |
Photodissociation of B–N Lewis adducts: a partially fused trinaphthylborane with dual fluorescence K Matsuo, S Saito, S Yamaguchi Journal of the American Chemical Society 136 (36), 12580-12583, 2014 | 166 | 2014 |
Facile synthesis of biphenyl-fused BODIPY and its property Y Hayashi, N Obata, M Tamaru, S Yamaguchi, Y Matsuo, A Saeki, S Seki, ... Organic letters 14 (3), 866-869, 2012 | 160 | 2012 |
Protonation‐Triggered Conformational Changes to Möbius Aromatic [32] Heptaphyrins (1.1. 1.1. 1.1. 1) S Saito, JY Shin, JM Lim, KS Kim, D Kim, A Osuka Angewandte Chemie International Edition 47 (50), 9657-9660, 2008 | 152 | 2008 |
Light-melt adhesive based on dynamic carbon frameworks in a columnar liquid-crystal phase S Saito, S Nobusue, E Tsuzaka, C Yuan, C Mori, M Hara, T Seki, ... Nature communications 7 (1), 12094, 2016 | 131 | 2016 |
A strap strategy for construction of an excited‐state intramolecular proton transfer (ESIPT) system with dual fluorescence N Suzuki, A Fukazawa, K Nagura, S Saito, H Kitoh‐Nishioka, ... Angewandte Chemie International Edition 53 (31), 8231-8235, 2014 | 129 | 2014 |
Conformational Planarization versus Singlet Fission: Distinct Excited‐State Dynamics of Cyclooctatetraene‐Fused Acene Dimers T Yamakado, S Takahashi, K Watanabe, Y Matsumoto, A Osuka, S Saito Angewandte Chemie 130 (19), 5536-5541, 2018 | 126 | 2018 |
Möbius antiaromatic bisphosphorus complexes of [30] hexaphyrins T Higashino, JM Lim, T Miura, S Saito, JY Shin, D Kim, A Osuka Angewandte Chemie International Edition 49 (29), 4950-4954, 2010 | 115 | 2010 |
Protonated [4n]π and [4n+2]π Octaphyrins Choose Their Möbius/Hückel Aromatic Topology JM Lim, JY Shin, Y Tanaka, S Saito, A Osuka, D Kim Journal of the American Chemical Society 132 (9), 3105-3114, 2010 | 114 | 2010 |
Boron-doped nanographene: Lewis acidity, redox properties, and battery electrode performance S Osumi, S Saito, C Dou, K Matsuo, K Kume, H Yoshikawa, K Awaga, ... Chemical Science 7 (1), 219-227, 2016 | 108 | 2016 |
Borylated dibenzoborepin: synthesis by skeletal rearrangement and photochromism based on bora-Nazarov cyclization. A Iida, S Saito, T Sasamori, S Yamaguchi Angewandte Chemie International Edition 52 (13), 2013 | 104 | 2013 |