Updated on 2026/09/14

写真a

 
IWAI Kento
 
Organization
Faculty of Advanced Engineering
Department
School of Engineering Department of Materials Chemistry
Title
Lecturer
External link

Message

  • 天然資源の新規活用法の開拓を指向した反応開発を行っています。主なテーマはC-O結合の切断反応の開発や反応活性な硫黄同素体の合成化学的な利用です。

Education

  • Kochi University of Technology

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  • Kochi University of Technology   School of Environmental Science and Engineering

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  • Kyoto University   Graduate School of Science   Division of Chemistry

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Degree

  • 博士(理学) ( 2021.3   京都大学 )

Research Field

  • Organic synthesis

  • Organometallic chemistry

  • Main group chemistry

Research Experience

  • The University of Shiga Prefecture   School of Engineering Department of Material Science   Lecturer

    2026.9

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  • Nara Women's University   Faculty Division of Natural Sciences   Assistant Professor

    2024.4 - 2026.8

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  • Kochi University of Technology   Assistant Professor

    2023.4 - 2024.3

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  • Kochi University of Technology   School of Environmental Science and Engineering   Assistant Professor

    2021.4 - 2023.3

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  • Japan Society for the Promotion of Science

    2020.4 - 2021.3

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Association Memberships

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Research Areas

  • Nanotechnology/Materials / Synthetic organic chemistry

  • Nanotechnology/Materials / Structural organic chemistry and physical organic chemistry

  • Nanotechnology/Materials / Inorganic/coordination chemistry

Papers

  • Mechanistic insight into the limited substrate scope of friedel–crafts-type anthracene formation using dichloromethane as a bridging reagent

    Nagatoshi Nishiwaki, Serika Ishida, Kento Iwai

    Journal of the Indian Chemical Society   2026.7

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.jics.2026.102599

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  • Unsymmetric d8-d8 Ir and Rh Dinuclear Complexes Formed with a Linear Tetraphosphine under Thermodynamic Control

    Takayuki Nakajima, Miwa Sato, Momoko Kotani, Yuki Maeda, Kento Iwai, Hajime Kameo, Tomoaki Tanase

    EUROPEAN JOURNAL OF INORGANIC CHEMISTRY   29 ( 16 )   2026.6

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/ejic.70189

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  • Takeda G Protein-Coupled Receptor 5 and Peroxisome Proliferator-Activated Receptor-Gamma Activation by Pinocembrin and Pinostrobin Isolated from Lindera sericea

    Ryo Miyata, Masanobu Suzuki, Yuka Okazaki, Kento Iwai, Nagatoshi Nishiwaki, Yoshihiro Nakajima

    International Journal of Molecular Sciences   2026.2

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.3390/ijms27042045

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  • 3-Azafluorenone Derivatives with Small HOMO-LUMO Gaps, Allowing Visible-Light Absorption

    Toshimichi Kobayashi, Yuki Itabashi, Kento Iwai, Tsuyoshi Inoue, Kei Ohkubo, Haruyasu Asahara

    CHEMISTRY-AN ASIAN JOURNAL   2025.11

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/asia.70415

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  • Copper Hydride Clusters with Cu<sub>9</sub> and Cu<sub>13</sub> Frameworks, Showing a Potential for Hydrogen Storage via Fluxional Exchange between Face-Capping and Interstitial Hydrides

    Takayuki Nakajima, Madoka Shimada, Yurika Komura, Seina Sakabe, Kanako Nakamae, Kento Iwai, Tomoaki Tanase

    INORGANIC CHEMISTRY   64 ( 39 )   19705 - 19718   2025.10

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.inorgchem.5c03167

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  • Regioselective Modification Distinguishing Slight Difference between Two C–Br Bonds in 1,7-Dibromonaphthalene and Synthesis of Unsymmetric Naphthalene Derivatives Reviewed

    Kento Iwai, Nana Hatayama, Akitaka Ito, Nagatoshi Nishiwaki

    The Journal of Organic Chemistry   2025.6

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    Authorship:Lead author   Publishing type:Research paper (scientific journal)   Publisher:American Chemical Society (ACS)  

    DOI: 10.1021/acs.joc.5c00680

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  • Synthesis of <i>ortho</i>-Nitrophenols with an Ester Functionality via Nitro Rearrangement

    Kento Iwai, Takumi Hamada, Nagatoshi Nishiwaki

    Journal of Oleo Science   2025

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.5650/jos.ess25139

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  • A Straightforward Synthesis of Pinocembrin Reviewed

    Kento Iwai, Nagatoshi Nishiwaki

    Journal of Oleo Science   2025

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.5650/jos.ess24245

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  • Synthesis of tricarbonylated propargylamine and conversion to 2,5-disubstituted oxazole-4-carboxylates Reviewed

    Iwai, K., Hikasa, A., Yoshioka, K., Tani, S., Umezu, K., Nishiwaki, N.

    Beilstein Journal of Organic Chemistry   20   2024.11

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.3762/bjoc.20.238

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  • Unsymmetric Ir<sub>2</sub> and RhIr Dinuclear Complexes Supported by a Linear Tetraphosphine meso-dpmppp, Showing High Reactivity for O<sub>2</sub>, H<sub>2</sub>, and HCl Reviewed

    Nakajima, T., Kotani, M., Maeda, Y., Sato, M., Iwai, K., Tanase, T.

    Inorganic Chemistry   63 ( 42 )   2024.10

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.inorgchem.4c03241

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  • Non‐Electronic Activation of Anthracenes Using Steric Repulsion of the 9‐Substituent with Chloro Groups at the peri‐Positions Reviewed

    Annisa Indah Reza, Kento Iwai, Nagatoshi Nishiwaki

    Asian Journal of Organic Chemistry   2024.8

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    We investigated how the introduction of substituent at the 9‐ or 10‐position of the 1,8‐dichloroanthracene framework affects the horizontal and vertical distortions of the anthracene rings. The 9‐substituted anthracenes showed higher distortions than their 10‐substituted counterparts due to the steric repulsion with two chloro groups at the peri‐positions. The distortion of anthracene framework affected their reactivity. Indeed, 9‐substituted anthracenes exhibited higher reactivity to undergo the Diels–Alder reaction with maleic anhydride, which was a result of non‐electronic activation.

    DOI: 10.1002/ajoc.202400381

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  • Unsymmetrization of 1,8-Dibromonaphthalenes by Acid-Induced Halogen Dance Reaction Reviewed

    Iwai, K., Nishiwaki, N.

    Journal of Organic Chemistry   89 ( 11 )   2024.6

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.joc.4c00507

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  • Highly electron-deficient 1-propyl-3,5-dinitropyridinium: evaluation of electron-accepting ability and application as an oxidative quencher for metal complexes Reviewed

    Ito, A., Kuroda, Y., Iwai, K., Yokoyama, S., Nishiwaki, N.

    RSC Advances   14 ( 9 )   2024

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1039/d4ra00845f

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  • Recent Progress in Haloalkene Synthesis by Hydrohalogenation (HX=HCl, HBr, HI) of Alkynes

    Iwai, K., Nishiwaki, N.

    Advanced Synthesis and Catalysis   366 ( 9 )   2024

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/adsc.202301499

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  • Cationic Iridium‐Catalyzed Decarboxylation of Aromatic Carboxylic Acids Reviewed International journal

    Reina Nonami, Yu Kishino, Tomokazu Yamasaki, Kazuya Kanemoto, Kento Iwai, Nagatoshi Nishiwaki, Kazutaka Shibatomi, Tomohiko Shirai

    Chemistry – An Asian Journal   18 ( 17 )   e202300533   2023.9

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    Language:English   Publishing type:Research paper (scientific journal)  

    Practical synthetic applications of catalytic decarboxylation in producing useful molecules are limited. We report herein the cationic Ir-catalyzed decarboxylations of various electron-rich and -poor aromatic carboxylic acids to produce hydrocarbons in good yield (up to >99%). Additionally, this reaction is applicable in decarboxylative hydroarylation of bicyclic alkenes and decarboxylative fluorination, indicating the potential utility of this catalytic decarboxylation in synthetic chemistry.

    DOI: 10.1002/asia.202300533

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  • Solid‐state Chromism of Zwitterionic Triarylmethylium Salts Reviewed

    Kento Iwai, Yoshiyuki Mizuhata, Tomoya Nakamura, Masato Goto, Atsushi Wakamiya, Yuichi Shimakawa, Norihiro Tokitoh

    European Journal of Inorganic Chemistry   2023.7

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/ejic.202300337

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  • Halo-Jacobsen Rearrangement Induced by Steric Repulsion between peri-Iodo Groups Reviewed International journal

    Kento Iwai, Noa Nishiguchi, Nagatoshi Nishiwaki

    The Journal of Organic Chemistry   88 ( 13 )   9409 - 9412   2023.7

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    Language:English   Publishing type:Research paper (scientific journal)  

    The naphthalene ring is distorted due to steric repulsion between iodo groups at the peri-positions. Due to the distortion, 1,8-diiodonaphthalene underwent a halo-Jacobsen rearrangement when treated with trifluoromethanesulfonic acid, producing 1,5-diiodonaphthalene and 1,4-diiodonaphthalene. In this reaction, acid-induced dehalogenative homocoupling also proceeded to form 4,4'-diiodo-1,1'-binaphthyl. The reaction selectivity could be controlled by varying the reaction temperature. DFT calculations and some control experiments revealed that these compounds were formed by different pathways.

    DOI: 10.1021/acs.joc.3c00165

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  • A Study of the Correlation between the Bulkiness of peri-Substituents and the Distortion of a Naphthalene Ring Reviewed

    Annisa Indah Reza, Kento Iwai, Nagatoshi Nishiwaki

    Molecules   28 ( 14 )   2023.7

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.3390/molecules28145343

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  • 2-Azafluorenone derivatives: Photocatalyst for oxygenation of toluene via electron transfer and hydrogen-atom transfer Reviewed

    Haruyasu Asahara, Yurie Horikawa, Kento Iwai, Nagatoshi Nishiwaki, Kei Ohkubo

    Journal of Photochemistry and Photobiology   15   2023.6

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.jpap.2023.100184

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  • Synthesis of Bis(functionalized) Aminals via Successive Nucleophilic Amidation and Amination Reviewed

    Kento Iwai, Akari Hikasa, Kotaro Yoshioka, Shinki Tani, Kazuto Umezu, Nagatoshi Nishiwaki

    The Journal of Organic Chemistry   88 ( 4 )   2207 - 2213   2023.2

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.joc.2c02647

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  • First synthesis of acylated nitrocyclopropanes. Reviewed International journal

    Kento Iwai, Rikiya Kamidate, Khimiya Wada, Haruyasu Asahara, Nagatoshi Nishiwaki

    Beilstein journal of organic chemistry   19   892 - 900   2023

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    Language:English   Publishing type:Research paper (scientific journal)  

    Although nitrocyclopropanedicarboxylic acid esters are widely used in organic syntheses, nitrocyclopropanes with an acyl group have not yet been synthesized. When adducts of β-nitrostyrene and 1,3-dicarbonyl compounds are treated with (diacetoxyiodo)benzene and tetrabutylammonium iodide, iodination occurs at the α-position of the nitro group, and the subsequent O-attack of the enol moiety leads to 2,3-dihydrofuran. Cyclopropane was successfully synthesized through C-attack as the acyl group became bulkier. The obtained nitrocyclopropane was transformed into furan upon treatment with tin(II) chloride via a ring-opening/ring-closure process.

    DOI: 10.3762/bjoc.19.67

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  • Synthesis of Unsymmetrical Ketones Using Chelation-Controlled Sequential Substitution of N-Triazinylamide/Weinreb Amide by Organometallic Reagents Reviewed

    Shotaro Hirao, Rumi Saeki, Toru Takahashi, Kento Iwai, Nagatoshi Nishiwaki, Yasushi Ohga

    ACS Omega   7 ( 51 )   48476 - 48483   2022.12

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acsomega.2c06756

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  • Synthesis and Characterization of Multiple Functionalized Cyclohexanone Using Diels–Alder Reaction of α-Nitrocinnamate Reviewed

    Hamada, T., Iwai, K., Nishiwaki, N.

    Reactions   3 ( 4 )   2022.12

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.3390/reactions3040041

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  • Recent Advances in Synthesis of Multiply Arylated/Alkylated Pyridines Reviewed

    Annisa Indah Reza, Kento Iwai, Nagatoshi Nishiwaki

    The Chemical Record   2022.9

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    Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    DOI: 10.1002/tcr.202200099

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  • Efficient synthesis of α-Nitro-β-Dialdimine ligands via Equilibrium–Controlling approach Reviewed

    Mahiro Nakabayashi, Nagatoshi Nishiwaki, Akitaka Ito, Shotaro Hayashi, Kento Iwai

    Tetrahedron Letters   102   2022.7

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1016/j.tetlet.2022.153948

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  • Unusual Reactivities of <i>ortho</i>-Hydroxy-β-nitrostyrene Reviewed

    Kento Iwai, Khimiya Wada, Nagatoshi Nishiwaki

    Molecules   27 ( 15 )   2022.7

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.3390/molecules27154804

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  • FeCl3-Promoted Facile Synthesis of Multiply Arylated Nicotinonitriles Reviewed

    Kento Iwai, Nagatoshi Nishiwaki, Haruka Yamauchi, Soichi Yokoyama

    Synthesis   54 ( 10 )   2480 - 2486   2022.5

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    Publishing type:Research paper (scientific journal)   Publisher:Georg Thieme Verlag {KG}  

    DOI: 10.1055/a-1731-9464

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  • Development of a synthetic equivalent of α,α-dicationic acetic acid leading to unnatural amino acid derivatives via tetrafunctionalized methanes Reviewed

    Haruyasu Asahara, Atsushi Bonkohara, Masaya Takagi, Kento Iwai, Akitaka Ito, Kotaro Yoshioka, Shinki Tani, Kazuto Umezu, Nagatoshi Nishiwaki

    Organic & Biomolecular Chemistry   20 ( 11 )   2282 - 2292   2022

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    Publishing type:Research paper (scientific journal)   Publisher:Royal Society of Chemistry ({RSC})  

    DOI: 10.1039/D1OB02482E

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  • A Mechanistic Study for Aziridination of Nitroalkenes Mediated by N-Chlorosuccinimide Reviewed

    Kento Iwai, Khimiya Wada, Feiyue Hao, Haruyasu Asahara, Nagatoshi Nishiwaki

    Journal of Oleo Science   71 ( 6 )   897 - 903   2022

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.5650/jos.ess21406

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  • A new approach to 10-arylated 5H-dibenzo[b,f]azepines using syn-selective hydrohalogenation of ethynylaniline Reviewed

    Kento Iwai, Yusuke Mukaijo, Haruyasu Asahara, Nagatoshi Nishiwaki

    Organic & Biomolecular Chemistry   20 ( 28 )   5543 - 5550   2022

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    Publishing type:Research paper (scientific journal)   Publisher:Royal Society of Chemistry ({RSC})  

    DOI: 10.1039/D2OB00950A

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  • Metal‐Free and syn‐Selective Hydrohalogenation of Alkynes through a Pseudo‐Intramolecular Process Reviewed

    Haruyasu Asahara, Yusuke Mukaijo, Kengo Muragishi, Kento Iwai, Akitaka Ito, Nagatoshi Nishiwaki

    European Journal of Organic Chemistry   2021 ( 42 )   5747 - 5755   2021.11

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/ejoc.202101134

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  • Alkali-Metal-Ion-Centered Sandwich Structures of 4-Bromophenyl[tris(pentafluorophenyl)]borates and Their Synthetic Utility Reviewed

    Kento Iwai, Yoshiyuki Mizuhata, Norihiro Tokitoh

    Organometallics   40 ( 5 )   570 - 577   2021.3

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.organomet.0c00711

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  • 2,2-Bis[3,5-bis(dimethylamino)phenyl]-1,1,1,3,3,3-hexamethyltrisilane Reviewed International journal

    Yoshiyuki Mizuhata, Kento Iwai, Norihiro Tokitoh

    IUCrData   5 ( 9 )   x201299   2020.9

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:International Union of Crystallography ({IUCr})  

    The title compound, C26H48N4Si3, was synthesized by the reaction of 2,2-di-chloro-tris-ilane with 3,5-bis-(di-methyl-amino)-phenyl-lithium. In the mol-ecule, the dihedral angle between the benzene rings is 57.57 (7)° and the Si-Si-Si bond angle is 110.08 (2)°. In the crystal, mol-ecules are linked via an SiC-H⋯π(ar-yl) inter-action, forming a chain along the c-axis direction.

    DOI: 10.1107/S2414314620012997

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  • Non-electronic aromatic ring activation by simple steric repulsion between substituents in 1-methylquinolinium salt systems Reviewed

    Kento Iwai, Soichi Yokoyama, Haruyasu Asahara, Nagatoshi Nishiwaki

    Bulletin of the Chemical Society of Japan   93 ( 1 )   50 - 57   2020

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1246/bcsj.20190263

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  • Development of a safely handleable synthetic equivalent of cyanonitrile oxide by 1,3-dipolar cycloaddition of nitroacetonitrile Reviewed

    Nagatoshi Nishiwaki, Yuta Kumegawa, Kento Iwai, Soichi Yokoyama

    Chemical Communications   55 ( 55 )   7903 - 7905   2019

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    Publishing type:Research paper (scientific journal)   Publisher:Royal Society of Chemistry ({RSC})  

    DOI: 10.1039/C9CC03875B

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  • Phosphine induced dimerization of propargyl alcohols leading to allyl propargyl ethers Reviewed

    Kento Iwai, Soichi Yokoyama, Haruyasu Asahara, Nagatoshi Nishiwaki

    Journal of Oleo Science   67 ( 6 )   773 - 778   2018

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.5650/jos.ess17277

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  • A direct synthesis of trisubstituted allenes from propargyl alcohols via oxaphosphetane intermediates Reviewed

    Kento Iwai, Soichi Yokoyama, Haruyasu Asahara, Nagatoshi Nishiwaki

    Bulletin of the Chemical Society of Japan   91 ( 3 )   337 - 342   2018

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1246/bcsj.20170372

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  • Synthesis of Functionalized 3-Cyanoisoxazoles Using a Dianionic Reagent Reviewed

    Kento Iwai, Haruyasu Asahara, Nagatoshi Nishiwaki

    Journal of Organic Chemistry   82 ( 10 )   5409 - 5415   2017.5

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    Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acs.joc.7b00811

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MISC

  • 蒼鉛(桑園)の繭:触媒利用への生糸を紡ぐ Invited

    月刊化学   77 ( 11月 )   2022.11

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    Authorship:Lead author  

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Awards

  • オレオマテリアル賞

    2023.9   日本油化学会   高反応性N-アシルイミンを合成素子とした多官能メタン類の合成

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Research Projects

  • マグネシウムクラスターを足場とするフェノール性水酸基の変換触媒の開発

    2026.6 - 2027.3

    公益財団法人 増屋記念基礎研究振興財団  助成金 

    岩井 健人

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    Authorship:Principal investigator 

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  • 芳香族カチオンを協働反応場とするフェノール水酸基の直接変換反応の開発

    2026.4 - 2027.3

    (公財)ENEOS東燃ゼネラル研究奨励・奨学会  研究助成 

    岩井 健人

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    Authorship:Principal investigator 

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  • 骨格歪みの解消を駆動力とするアレーン遷移金属触媒の開発

    Grant number:25K18051  2025.4 - 2028.3

    日本学術振興会  科学研究費助成事業  若手研究

    岩井 健人

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    Grant amount:\4940000 ( Direct Cost: \3800000 、 Indirect Cost:\1140000 )

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  • アニオン性置換基導入による高周期元素低配位化学種の酸化電位および構造の制御

    Grant number:20J12946  2020.4 - 2022.3

    日本学術振興会  科学研究費助成事業  特別研究員奨励費

    岩井 健人

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    Grant amount:\1700000 ( Direct Cost: \1700000 )

    申請者の2020年度における研究計画では、ボラヌイジル基を有する高周期典型元素低配位化学種を合成し、物性の評価を行なうことで、ボラヌイジル基の置換基効果を解明することを目標としていた。実際の研究では、ボラヌイジル基を有する双性イオン型トリアリールメチリウム塩やアクリジニウム塩およびケイ素化合物を新たに合成し、物性や反応性の評価を行なった。その結果、双性イオン型のトリアリールメチリウム塩が外部刺激に応答した色調の変化を示すことや、アクリジニウム塩が固体状態でのみ発光を示すことを明らかにした。これらの双性イオン型の色素について、単結晶X線構造解析など各種測定を行なったところ、ボラヌイジル基のイオン性相互作用に起因する特異な分子配列を示していることがわかった。この結果から、ボラヌイジル基の置換基効果として、分子内の電子的な効果のみならず、固体状態での分子間の集積構造を制御する効果があると考えられる。従って、ボラヌイジル基の新たな活用法として分子配列の制御が可能であることを示した点で本研究成果は意義深いといえる。
    さらにボラヌイジル基を有する低配位ケイ素化学種の合成検討では、ボラヌイジル基を有するクロロシラン類にN-ヘテロ環状カルベン(NHC)を作用させると塩脱離を伴う求核置換反応が進行することを見出した。これは一般的なシラン類では見られない反応性であり、ボラヌイジル基を導入したことにより発現した新規な反応性であると考えられる。また、本置換反応により生成するイミダゾリオシランは更なる化学変換により多座配位性の配位場を有するアニオン性NHCへ変換できることを明らかにした。これらの一連の反応は近年注目を集めているアニオン性NHCの新規な合成法と見做せるため、合成化学的な観点から意義深い結果であると考えられる。

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Teaching Experience

  • 固体化学入門

    2025.4 - 2026.8 Institution:奈良女子大学

  • 有機金属化学III

    2024.4 - 2026.8 Institution:奈良女子大学

  • 化学基礎実験3

    2024.4 - 2026.8 Institution:奈良女子大学

Academic Contribution

  • ハロゲン利用ミニシンポジウム2023 事務局

    Role(s): Planning, management, etc.

    西脇 永敏  2023.12

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    Type:Competition, symposium, etc. 

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  • 日本油化学会第61回年会 実行委員会事務局

    Role(s): Planning, management, etc.

    西脇 永敏  2023.9

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  • 日本化学会中四国支部2021年日本化学会中四国支部大会 高知大会 実行委員

    Role(s): Planning, management, etc.

    小廣 和哉  2021.11

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    Type:Competition, symposium, etc. 

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