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OTA Kei
| Material Science Division | Assistant Professor |
| Chemistry |
- E-Mail:keiota
mail.saitama-u.ac.jp - Home Page:
Researcher information
■ Degree■ Research Keyword
- Inorganic chemistry
- organic chemistry
- Organoelemental chemistry
- Main group element
- Aromatics
- Silicon
- Boron
- Nanotechnology/Materials, Structural/physical organic chemistry
- Nanotechnology/Materials, Inorganic and coordination chemistry
- Apr. 2025 - Present, Saitama University, Graduate School of Science and Engineering, Assistant professor
- Apr. 2022 - Mar. 2024, Kindai University, Faculty of Science and Engineering Department of Applied Chemistry, Assistant professor
- Oct. 2021 - Mar. 2022, Nanyang Technological University, Research fellow
- Mar. 2021 - Oct. 2021, Nanyang Technological University, Student assistant
- Aug. 2017 - Sep. 2021, Nanyang Technological University, School of Physical and Mathematical Sciences, Chemistry and Biological Chemistry, Singapore
- Apr. 2013 - Mar. 2017, University of Tsukuba, School of Science and Engineering, College of Chemistry, Japan
- May 2024, The 3rd Marie Sklodowska Curie Award, Inspiration Prize, JST, Embassy of the Republic of Poland
Kei Ota - Sep. 2020, Poster award sponsored by Chemical Science, Sigma-bonding between Two pai-Orbitals in Zwitterionic Inorganic Benzene Valence Isomer, Nanyang Research Conference on Synthetic Chemistry and Catalysis
International society, Singapore - Jul. 2019, Poster award, Zwitterionic Inorganic Benzene Valence Isomer with sigma-Bonding between Two pai-Orbitals, The 5th Singapore Inorganic Chemistry Symposium
Kei Ota, International society, Singapore - Jul. 2019, Excellent poster award, Zwitterionic Inorganic Benzene Valence Isomer with sigma-Bonding between Two pai-Orbitals, The 2nd International Conference on Boron Chemistry
Kei Ota, International society, China - Aug. 2017, Singapore International Graduate Award (SINGA), Agency for Science, Technology & Research (A*STAR)
Others, Singapore
Performance information
■ Paper- Synthesis and characterization of a diarylstannylene bearing (MeO)EPind groups and its oxidation reactions
Yuto Ueno; Mizuki Imai; Yuki Maehara; Kotomi Matsui; Yuria Kawase; Kei Ota; Daisuke Hashizume; Tsukasa Matsuo
Bulletin of the Chemical Society of Japan, Volume:98, Number:11, Oct. 2025, [Reviewed]
Abstract
A new diarylstannylene, [(MeO)EPind]2Sn: (1), has been synthesized and isolated using a novel protecting group, (MeO)EPind, which incorporates an electron-donating methoxy chain at the para position of the EPind group. The structure and electronic properties of 1 were investigated using crystallographic and spectroscopic methods as well as DFT calculations. The reaction of 1 with N2O gas produced a diarylstannanone, [(MeO)EPind]2Sn=O (2), which subsequently reacted with H2O to afford a stannanediol, [(MeO)EPind]2Sn(OH)2 (3). We also examined the reaction of 1 with elemental sulfur (S8), which resulted in the formation of a mixture containing diarylstannanethione, [(MeO)EPind]2Sn=S (4) and 1,2,3,4,5-tetrathiastannolane, [(MeO)EPind]2SnS4 (5). The structural features and bonding nature of these Sn(IV) compounds have been both experimentally and theoretically characterized.
Oxford University Press (OUP), Scientific journal
DOI:https://doi.org/10.1093/bulcsj/uoaf104
DOI ID:10.1093/bulcsj/uoaf104, ISSN:0009-2673, eISSN:1348-0634 - Organoantimony(I) Compounds Incorporating the Bulky Rind Groups: Selective Synthesis and Characterization of Distibene and Cyclotetrastibane
Yuria Kawase; Kei Ota; Shotaro Ikoma; Kiyoto Sugahara; Tsukasa Nakahodo; Yoshiyuki Mizuhata; Tsukasa Matsuo
Organometallics, Volume:44, Number:19, First page:2240, Last page:2249, Sep. 2025, [Reviewed]
American Chemical Society (ACS), Scientific journal
DOI:https://doi.org/10.1021/acs.organomet.5c00264
DOI ID:10.1021/acs.organomet.5c00264, ISSN:0276-7333, eISSN:1520-6041 - Flash Communication: Exocyclic Alkenyl Tuning of Cyclic (Amino)carbene: Enhancing π-Acceptor Property without Ring Unsaturation
Masaru Tanaka; Shota Kamiyama; Kei Ota; Norio Nakata
Organometallics, Volume:44, Number:14, First page:1510, Last page:1514, Jul. 2025, [Reviewed]
American Chemical Society (ACS), Scientific journal
DOI:https://doi.org/10.1021/acs.organomet.5c00200
DOI ID:10.1021/acs.organomet.5c00200, ISSN:0276-7333, eISSN:1520-6041 - A Monomeric Diarylstannanone with a Sn=O Double Bond: Synthesis and Characterization
Tomoharu Tanikawa; Yuto Ueno; Shigeaki Konaka; Yasuyuki Numata; Mizuki Imai; Kei Ota; Hiroyuki Fueno; Kazuyoshi Tanaka; Daisuke Hashizume; Tsukasa Matsuo
Chemistry – An Asian Journal, May 2025, [Reviewed]
Scientific journal
DOI:https://doi.org/10.1002/asia.202401847
DOI ID:10.1002/asia.202401847, ORCID:179740010 - Reactions of Halogermylenes with N‐Heterocyclic Carbenes: Selective Formation of Low Valent Ge(II) Species
Kei Ota; Shotaro Ikoma; Tomohisa Okuda; Taisei Itakura; Tsukasa Nakahodo; Daisuke Hashizume; Tsukasa Matsuo
European Journal of Organic Chemistry, Apr. 2025, [Reviewed], [Lead, Corresponding]
The reactions of the Rind‐based 1,2‐dihalodigermenes, (Eind)BrGe=GeBr(Eind) (1a), and (EMind)ClGe=GeCl(EMind) (1b), with two types of N‐heterocyclic carbenes (NHCs) (Im‐iPr2Me2 and Im‐Me4) result in the formation of the halogermylene mono‐NHC adducts, (Im‐iPr2Me2)(Eind)GeBr (2a') and (Im‐iPr2Me2)(EMind)GeCl (2b'), and the germyliumylidene cation bis‐NHC adducts, [(Im‐Me4)2(Eind)Ge]+[Br−] (3a) and [(Im‐Me4)2(EMind)Ge]+[Cl−] (3b). The resulting Ge(II) species are stabilized by the bulky Rind groups and the strongly σ‐donating NHC ligands, whose structures are confirmed by a single‐crystal X‐ray diffraction (SC‐XRD) analysis. Based on density functional theory (DFT) and quantum theory of atoms in molecules (QTAIM) calculations of 2a’ and the cationic part of 3a, it is concluded that while the GeC(Eind) and GeC(NHC) bonds exhibit distinct differences in their degrees of polarization, all the GeC bonds display a partially polarized covalent character. Both reaction energy calculations and experimental studies suggested the potential liberation of an NHC ligand from the germyliumylidene cation bis‐NHC adducts, leading to the exchange of the NHC ligands. The formation mechanism of 3a from 1a and two NHC molecules via (Im‐Me4)(Eind)GeBr (2a) is discussed based on DFT calculations.
Wiley, Scientific journal
DOI:https://doi.org/10.1002/ejoc.202500112
DOI ID:10.1002/ejoc.202500112, ISSN:1434-193X, eISSN:1099-0690, ORCID:181809941 - Silicon Analogues of Cyclopropyl Radical Derived from a Highly Stable Cyclic Disilene Compound Featuring a Si–Br Bond
Ryoma Ohno; Kei Ota; Nagisa Nishimura; Kanta Taniguchi; Shuma Kurokawa; Tomonari Wakabayashi; Miho Hatanaka; Alfredo Rosas-Sánchez; Daisuke Hashizume; Tsukasa Matsuo
Journal of the American Chemical Society, Volume:146, Number:36, First page:24911, Last page:24924, Aug. 2024, [Reviewed], [Corresponding]
American Chemical Society (ACS), Scientific journal
DOI:https://doi.org/10.1021/jacs.4c06111
DOI ID:10.1021/jacs.4c06111, ISSN:0002-7863, eISSN:1520-5126 - Approach to the “Missing” Diarylsilylene: Formation, Characterization, and Intramolecular C–H Bond Activation of Blue Diarylsilylenes with Bulky Rind Groups
Kazuki Mochihara; Tatsuto Morimoto; Kei Ota; Shinsuke Marumoto; Daisuke Hashizume; Tsukasa Matsuo
International Journal of Molecular Sciences, Volume:25, Number:7, First page:3761, Last page:3761, Mar. 2024, [Reviewed]
The treatment of the bulky Rind-based dibromosilanes, (Rind)2SiBr2 (2) [Rind = 1,1,7,7-tetra-R1-3,3,5,5-tetra-R2-s-hydrindacen-4-yl: EMind (a: R1 = Et, R2 = Me) and Eind (b: R1 = R2 = Et)], with two equivalents of tBuLi in Et2O at low temperatures resulted in the formation of blue solutions derived from the diarylsilylenes, (Rind)2Si: (3). Upon warming the solutions above −20 °C, the blue color gradually faded, accompanying the decomposition of 3 and yielding cyclic hydrosilanes (4) via intramolecular C–H bond insertion at the Si(II) center. The molecular structures of the bulky Eind-based 3b and 4b were confirmed by X-ray crystallography. Thus, at −20 °C, blue crystals were formed (Crystal-A), which were identified as mixed crystals of 3b and 4b. Additionally, colorless crystals of 4b as a singular component were isolated (Crystal-B), whose structure was also determined by an X-ray diffraction analysis. Although the isolation of 3 was difficult due to their thermally labile nature, their structural characteristics and electronic properties were discussed based on the experimental findings complemented by computational results. We also examined the hydrolysis of 3b to afford the silanol, (Eind)2SiH(OH) (5b).
MDPI AG, Scientific journal
DOI:https://doi.org/10.3390/ijms25073761
DOI ID:10.3390/ijms25073761, eISSN:1422-0067, ORCID:156724167 - Selective monooxygenation of diphosphenes with molecular oxygen
Yuria Kawase; Shota Tsujimoto; Tomohiro Obayashi; Satoshi Kimura; Kanta Ito; Shotaro Ikoma; Kei Ota; Daisuke Hashizume; Tsukasa Matsuo
Dalton Transactions, Volume:53, Number:5, First page:1956, Last page:1960, 2024, [Reviewed]
The O2 splitting mediated by the bulky Rind-based diphosphenes leads to the clean formation of the diphosphene oxides with (O)PP moieties.
Royal Society of Chemistry (RSC), Scientific journal
DOI:https://doi.org/10.1039/d3dt04348g
DOI ID:10.1039/d3dt04348g, ISSN:1477-9226, eISSN:1477-9234, ORCID:151003817 - A Series of Lithium Complexes of Bulky Rind-based Arylthiolate Ligands: Synthesis, Characterization, and Crystal Structures
Masahiro Hamura; Kohei Sugano; Ryo Matsukura; Kei Ota; Tsukasa Nakahodo; Daisuke Hashizume; Tsukasa Matsuo
Chemistry Letters, Volume:52, Number:3, First page:140, Last page:143, Mar. 2023, [Reviewed]
The bulky Rind-based thiols, (Rind)SH (1) [Rind = 1,1,7,7-tetra-R1-3,3,5,5-tetra-R2-s-hydrindacen-4-yl: EMind (a: R1 = Et, R2 = Me), Eind (b: R1 = R2 = Et), and MPhind (c: R1 = Me, R2 = Ph)], reacted with nBuLi in THF to afford a series of lithium arylthiolates, [(Rind)SLi]n(THF)m (2), whose structures were confirmed by an X-ray diffraction analysis. In the solid state, while the less bulky EMind-based lithium thiolate exhibited a linear dimer, [(EMind)SLi]2(THF)4 (2a), or trimer, [(EMind)SLi]3(THF)5 (2a′), the monomeric structures of (Eind)SLi(THF)3 (2b) and (MPhind)SLi(THF)2 (2c) were found for the bulky Eind- and the bulkier MPhind-based systems. The salt metathesis reaction between 2a and FeCl2(THF)1.5 in THF produced the anionic three-coordinate planar Fe(II) thiolate complex, [Li(THF)3][{(EMind)S}3Fe] (3a).
The Chemical Society of Japan, Scientific journal
DOI:https://doi.org/10.1246/cl.220532
DOI ID:10.1246/cl.220532, ISSN:0366-7022, eISSN:1348-0715, ORCID:139996761 - A series of (E)-1,2-diaryldigermenes incorporating bulky Eind groups: structural characteristics and absorption properties
Shogo Yagura; Naoki Hayakawa; Airi Kuroda; Kei Ota; Rhota Tanishita; Genya Urasaki; Tsukasa Nakahodo; Hidetaka Nakai; Manabu Hoshino; Daisuke Hashizume; Tsukasa Matsuo
Dalton Transactions, Volume:51, Number:48, First page:18633, Last page:18641, Nov. 2022, [Reviewed]
We present the synthesis, structural features and absorption properties of a series of (E)-1,2-diaryldigermenes supported by the fused-ring bulky Eind groups.
Royal Society of Chemistry (RSC), Scientific journal
DOI:https://doi.org/10.1039/d2dt03427a
DOI ID:10.1039/d2dt03427a, ISSN:1477-9226, eISSN:1477-9234, ORCID:123829486 - Formation and Reactions of Ge=O Double-bonded Species Bearing EMind Groups
Airi Kuroda; Naoko Fujita; Tomomi Horita; Kei Ota; Alfredo Rosas-S{\'{a } }nchez; Manabu Hoshino; Daisuke Hashizume; Tsukasa Matsuo
Chemistry Letters, Volume:51, Number:8, First page:828, Last page:831, Aug. 2022, [Reviewed]
The Chemical Society of Japan, English, Scientific journal
DOI:https://doi.org/10.1246/cl.220222
DOI ID:10.1246/cl.220222, ISSN:0366-7022, ORCID:120876564 - Zero-valent species of group 13–15 elements
Kei Ota; Rei Kinjo
Chem, Volume:8, Number:2, First page:340, Last page:350, Feb. 2022, [Reviewed], [Lead]
Elsevier BV, Scientific journal
DOI:https://doi.org/10.1016/j.chempr.2022.01.010
DOI ID:10.1016/j.chempr.2022.01.010, ISSN:2451-9294, ORCID:111475828 - A Crystalline B4N2 Dewar Benzene as a Building Block for Conjugated B,N-Chains
Kei Ota; Rei Kinjo
Journal of the American Chemical Society, Volume:143, Number:29, First page:11152, Last page:11159, Jul. 2021, [Reviewed], [Lead]
American Chemical Society (ACS), Scientific journal
DOI:https://doi.org/10.1021/jacs.1c04860
DOI ID:10.1021/jacs.1c04860, ISSN:0002-7863, eISSN:1520-5126, ORCID:97045281 - Open questions in boron species with globally 4n π systems
Kei Ota; Rei Kinjo
Communications Chemistry, Volume:4, Number:1, Jul. 2021, [Reviewed], [Lead]
Springer Science and Business Media LLC, Scientific journal
DOI:https://doi.org/10.1038/s42004-021-00542-x
DOI ID:10.1038/s42004-021-00542-x, eISSN:2399-3669, ORCID:96913538 - Heavier element-containing aromatics of [4n+2]-electron systems
Kei Ota; Rei Kinjo
Chemical Society Reviews, Volume:50, Number:18, First page:10594, Last page:10673, 2021, [Reviewed], [Lead]
This review focuses on the heavier group 13–15 element-containing heterocycles of [4n+2]-electron systems featuring classical and advanced aromatics.
Royal Society of Chemistry (RSC), Scientific journal
DOI:https://doi.org/10.1039/d0cs01354d
DOI ID:10.1039/d0cs01354d, ISSN:0306-0012, eISSN:1460-4744, ORCID:98235239 - Aromatic nature of neutral and dianionic 1,4-diaza-2,3,5,6-tetraborinine derivatives
Kei Ota; Rei Kinjo
RSC Advances, Volume:11, Number:1, First page:592, Last page:598, 2021, [Reviewed], [Lead]
Royal Society of Chemistry ({RSC}), Scientific journal
DOI:https://doi.org/10.1039/D0RA09040A
DOI ID:10.1039/D0RA09040A, ORCID:86185630 - Inorganic Benzene Valence Isomers
Kei Ota; Rei Kinjo
Chemistry – An Asian Journal, Volume:15, Number:17, First page:2558, Last page:2574, Sep. 2020, [Reviewed], [Lead]
Wiley, Scientific journal
DOI:https://doi.org/10.1002/asia.202000535
DOI ID:10.1002/asia.202000535, ORCID:78491316 - A Neutral and Aromatic Boron‐Rich Inorganic Benzene
Kei Ota; Rei Kinjo
Angewandte Chemie International Edition, Volume:59, Number:16, First page:6572, Last page:6575, Apr. 2020, [Reviewed], [Lead]
Wiley, English, Scientific journal
DOI:https://doi.org/10.1002/anie.201915790
DOI ID:10.1002/anie.201915790, ISSN:1433-7851, ORCID:96101383 - Germylone-bridged bimetallic Ir and Rh complexes
Bochao Su; Kei Ota; Yongxin Li; Rei Kinjo
Dalton Transactions, Volume:48, Number:11, First page:3555, Last page:3559, 2019, [Reviewed]The reactions of germylone
1 with one equivalent of [M(COD)Cl]2 (M = Ir, Rh) afforded the germylone-bridged bimetallic complexes2 and3 , which have been spectroscopically and structurally characterized.
Royal Society of Chemistry ({RSC}), English, Scientific journal
DOI:https://doi.org/10.1039/c9dt00145j
DOI ID:10.1039/c9dt00145j, ISSN:1477-9226, ORCID:96101384 - Zwitterionic Inorganic Benzene Valence Isomer with σ-Bonding between Two π-Orbitals
Bochao Su; Kei Ota; Kai Xu; Hajime Hirao; Rei Kinjo
Journal of the American Chemical Society, Volume:140, Number:38, First page:11921, Last page:11925, Sep. 2018, [Reviewed]
American Chemical Society ({ACS}), English, Scientific journal
DOI:https://doi.org/10.1021/jacs.8b08025
DOI ID:10.1021/jacs.8b08025, ISSN:0002-7863, ORCID:96101379 - Bis(stibahousene)
Vladimir Ya. Lee; Kei Ota; Yuki Ito; Olga A. Gapurenko; Akira Sekiguchi; Ruslan M. Minyaev; Vladimir I. Minkin; Heinz Gornitzka
Journal of the American Chemical Society, Volume:139, Number:39, First page:13897, Last page:13902, Oct. 2017, [Reviewed]
American Chemical Society ({ACS}), English, Scientific journal
DOI:https://doi.org/10.1021/jacs.7b07712
DOI ID:10.1021/jacs.7b07712, ISSN:0002-7863, ORCID:96101376
- Synthesis of Heavier Group 14 Element Cations
Kei Ota; Shotaro Ikoma; Tomohisa Okuda; Tsukasa Matsuo
Sep. 2024 - Reaction of arylhalogermylenes with NHCs
Kei Ota; Shotaro Ikoma; Tsukasa Matsuo
The 14th International Conference on Heteroatom Chemistry (ICHAC-14), Jul. 2024, [Invited] - Synthesis and reduction of aryl cyclotrisilenylium ion
K. Ota; R. Ohno; N. Nishimura; T. Matsuo
20th International Symposium on Silicon Chemistry (ISOS-20), May 2024 - アリール基を有する シクロトリシレニルカチオンの合成
太田圭; 大野稜真; 松尾司
Dec. 2022 - Synthesis and Characterization of Boron-Rich Inorganic Benzene
太田圭; 金城玲
Dec. 2020 - Synthesis, Characterization and Reactivities of Boron-Rich Dewar Benzene
Kei Ota; Rei Kinjo
Dec. 2020 - Unexpected σ-bonding between two π-orbitals on the boron rich inorganic benzene valence isomer
Kei Ota
PhD Student Workshop in Organic Chemistry, Nov. 2019 - Zwitterionic Inorganic Benzene Valence Isomer with sigma-Bonding between Two pai-Orbitals
Kei Ota; Bochao Su; Kai Xu; Hajime Hirao; Rei Kinjo
Chemistry National Meeting Singapore (ChnmSG 2019), May 2019
- Apr. 2023 - Mar. 2024
科学技術英語2 - Apr. 2023 - Mar. 2024
アドバンスト有機化学 - Apr. 2022 - Mar. 2024
基礎ゼミI・II - Apr. 2022 - Mar. 2024
応用化学実験IV - Apr. 2022 - Mar. 2023
応用化学実験II
■ Research projects
- ホウ素0価単原子の創出とホウ素トランスファー反応への展開
01 Apr. 2024 - 31 Mar. 2026
Grant amount(Total):4680000, Direct funding:3600000, Indirect funding:1080000
Grant number:24K17700 - 13族元素0価化学種の創出と元素トランスファー反応への展開
Aug. 2022 - Mar. 2024
Grant amount(Total):2860000, Direct funding:2200000, Indirect funding:660000
Grant number:22K20561
