Kyoko Nozaki 研究室
主宰者:Kyoko Nozaki
東京大学
AI 要約(直近 5 年の研究成果)
野崎研究室は、触媒化学と有機金属化学を基盤として、プラスチック廃棄物の資源化と新規材料設計に取り組んでいます。プラスチックのリサイクルでは、混合廃棄物から特定のポリマーを選別分解する触媒法や、ポリエチレンなどの難分解性高分子を化学的・光化学的に分解する方法を開発しています。これらの研究では、イリジウムやニッケル、パラジウムなどの遷移金属触媒を活用し、酸素含有官能基の除去や炭素-酸素結合の選択的切断を実現しています。
同時に、新たな結晶性材料や高機能分子の創製にも注力しています。ランタノイドやイットリウムなどの希土類金属とカスタマイズされた有機配位子を組み合わせた錯体の設計・合成を行い、これらの光学特性や磁性を解析しています。また、遷移金属とカルベン類などの特異な有機リガンドの相互作用、および金属と配位子の協働による反応機構の研究も進めています。
これらの多角的なアプローチを通じて、野崎研究室は「不要になった物質を有用な化学品へ変換する触媒開発」と「金属-有機分子の相互作用を深く理解し、新機能を持つ材料を設計する」という二つの大きなテーマで、化学的課題解決に貢献しています。
※ AI(Claude)が、公開されている論文要旨から研究の問い・手法・主要な発見を事実情報として抽出・再構成して自動生成しています。誤りを含む可能性があるため、正確性は研究室公式情報でご確認ください。
外部リンク
関連研究室(8 件)
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研究成果(191 件)
- [2026] Selective Degradation of Polyurethanes in Mixed Plastic Wastes via Ir-Catalyzed HydrogenolysisDOI: https://doi.org/10.26434/chemrxiv.15000212/v1
- DOI: https://doi.org/10.26434/chemrxiv.15002999/v1
- DOI: https://doi.org/10.26434/chemrxiv.15002999/v1
- DOI: https://doi.org/10.1021/acs.inorgchem.5c04538
- DOI: https://doi.org/10.5059/yukigoseikyokaishi.83.1066
- DOI: https://doi.org/10.1039/d5sc90244d
- DOI: https://doi.org/10.1021/acs.organomet.4c00462
- DOI: https://doi.org/10.1038/s41467-025-56488-4
- DOI: https://doi.org/10.1039/d5sc90244d
- DOI: https://doi.org/10.1021/acs.organomet.4c00462
続きを表示(残り 181 件)閉じる
- DOI: https://doi.org/10.1038/s41467-025-56488-4
- DOI: https://doi.org/10.1021/acsmacrolett.4c00726
- DOI: https://doi.org/10.1016/j.tet.2025.134560
- DOI: https://doi.org/10.1021/acs.organomet.5c00006
- DOI: https://doi.org/10.1016/j.tet.2025.134560
- DOI: https://doi.org/10.1021/acsmacrolett.4c00726
- DOI: https://doi.org/10.1039/d5fd90051d
- DOI: https://doi.org/10.1039/d5fd90052b
- DOI: https://doi.org/10.1021/acs.inorgchem.5c04538
- DOI: https://doi.org/10.1039/d5fd90054a
- DOI: https://doi.org/10.1021/acs.orglett.5c01708
- DOI: https://doi.org/10.1021/acs.joc.5c02123
- DOI: https://doi.org/10.5059/yukigoseikyokaishi.83.1006
- DOI: https://doi.org/10.1093/bulcsj/uoaf108
- DOI: https://doi.org/10.1021/acsmacrolett.5c00476
- DOI: https://doi.org/10.1038/s41467-025-62409-2
- [2025] Synthesis and characterization of stable nickel( <scp>ii</scp> ) complexes bearing long alkyl chainsDOI: https://doi.org/10.1039/d5fd00083a
- DOI: https://doi.org/10.1021/acs.joc.5c01153
- DOI: https://doi.org/10.1021/acs.joc.5c02123
- DOI: https://doi.org/10.5059/yukigoseikyokaishi.83.1006
- DOI: https://doi.org/10.1021/acsmacrolett.5c00476
- DOI: https://doi.org/10.1038/s41467-025-62409-2
- DOI: https://doi.org/10.1002/anie.202503322
- DOI: https://doi.org/10.1002/anie.202503322
- DOI: https://doi.org/10.1002/ange.202503322
- DOI: https://doi.org/10.1002/ange.202503322
- DOI: https://doi.org/10.1021/acs.inorgchem.5c00532
- DOI: https://doi.org/10.1021/acs.inorgchem.5c00532
- DOI: https://doi.org/10.1021/acs.orglett.5c01708
- DOI: https://doi.org/10.1021/acs.inorgchem.5c01184
- [2025] Polyethyleneketones with Controlled Spacer Units: Synthesis, Characterization, and PhotodegradationDOI: https://doi.org/10.1021/jacs.5c01664
- [2025] Exploring biodegradation limits of n-alkanes as polyethylene models using multi-omics approachesDOI: https://doi.org/10.1016/j.scitotenv.2025.179365
- DOI: https://doi.org/10.1021/acs.organomet.5c00006
- DOI: https://doi.org/10.1021/acs.inorgchem.5c01184
- [2025] Exploring biodegradation limits of n-alkanes as polyethylene models using multi-omics approachesDOI: https://doi.org/10.1016/j.scitotenv.2025.179365
- [2025] Polyethyleneketones with Controlled Spacer Units: Synthesis, Characterization, and PhotodegradationDOI: https://doi.org/10.1021/jacs.5c01664
- DOI: https://doi.org/10.1039/d5fd90051d
- DOI: https://doi.org/10.1039/d5fd90052b
- DOI: https://doi.org/10.1002/chem.202402323
- DOI: https://doi.org/10.1021/jacs.4c02531
- DOI: https://doi.org/10.1002/marc.202400742
- DOI: https://doi.org/10.1021/jacs.4c12732
- DOI: https://doi.org/10.1002/marc.202400742
- DOI: https://doi.org/10.1021/jacs.4c12732
- DOI: https://doi.org/10.1021/jacs.4c02531
- DOI: https://doi.org/10.1021/acs.inorgchem.4c03514
- DOI: https://doi.org/10.1021/acs.macromol.4c01250
- DOI: https://doi.org/10.1002/ceur.202400053
- DOI: https://doi.org/10.1002/chem.202402323
- DOI: https://doi.org/10.1021/jacs.4c07445
- DOI: https://doi.org/10.1021/acs.inorgchem.4c03514
- DOI: https://doi.org/10.1021/acs.macromol.4c01250
- DOI: https://doi.org/10.1002/ceur.202400053
- DOI: https://doi.org/10.1021/jacs.4c07445
- DOI: https://doi.org/10.1021/acsapm.4c01691
- DOI: https://doi.org/10.1021/jacs.4c06553
- DOI: https://doi.org/10.1021/acs.orglett.4c01971
- DOI: https://doi.org/10.1002/anie.202410849
- DOI: https://doi.org/10.1002/ange.202410849
- DOI: https://doi.org/10.1021/jacs.4c07458
- DOI: https://doi.org/10.1002/chem.202401860
- [2024] Synthesis of Novel Polymers with Biodegradability by Main-Chain Editing of Chiral PolyketonesDOI: https://doi.org/10.1021/jacs.4c04389
- DOI: https://doi.org/10.1021/acs.joc.4c00538
- DOI: https://doi.org/10.1021/acsapm.4c01691
- DOI: https://doi.org/10.1021/jacs.4c06553
- DOI: https://doi.org/10.1021/acs.orglett.4c01971
- DOI: https://doi.org/10.1002/anie.202410849
- DOI: https://doi.org/10.1002/ange.202410849
- DOI: https://doi.org/10.1021/jacs.4c07458
- DOI: https://doi.org/10.1002/chem.202401860
- [2024] Synthesis of Novel Polymers with Biodegradability by Main-Chain Editing of Chiral PolyketonesDOI: https://doi.org/10.1021/jacs.4c04389
- DOI: https://doi.org/10.1021/acs.joc.4c00538
- DOI: https://doi.org/10.1021/acs.organomet.4c00032
- DOI: https://doi.org/10.1021/acs.organomet.4c00032
- DOI: https://doi.org/10.1002/chem.202400586
- DOI: https://doi.org/10.1002/anie.202403092
- DOI: https://doi.org/10.1002/ange.202403092
- DOI: https://doi.org/10.1038/s41428-023-00867-5
- DOI: https://doi.org/10.1039/d4sc05928j
- DOI: https://doi.org/10.1295/kobunshi.73.10_501
- DOI: https://doi.org/10.1002/chem.202400586
- DOI: https://doi.org/10.1002/anie.202403092
- DOI: https://doi.org/10.1002/ange.202403092
- DOI: https://doi.org/10.1038/s41428-023-00867-5
- DOI: https://doi.org/10.1039/d4sc05928j
- DOI: https://doi.org/10.1295/kobunshi.73.10_501
- DOI: https://doi.org/10.1021/jacs.2c11145
- DOI: https://doi.org/10.1002/chem.202302060
- DOI: https://doi.org/10.1021/acs.organomet.3c00135
- DOI: https://doi.org/10.1039/d3qo01162c
- DOI: https://doi.org/10.1039/d3cc02292g
- DOI: https://doi.org/10.1039/d3sc04837c
- DOI: https://doi.org/10.1039/d3sc04837c
- DOI: https://doi.org/10.1039/d3cc02292g
- DOI: https://doi.org/10.1039/d3qo01162c
- [2023] A dinuclear Rh(− <scp>i</scp> )/Rh( <scp>i</scp> ) complex bridged by biphilic phosphinine ligandsDOI: https://doi.org/10.1039/d3sc02292g
- DOI: https://doi.org/10.1021/jacs.3c09061
- DOI: https://doi.org/10.1002/chem.202303575
- DOI: https://doi.org/10.1021/jacs.3c09061
- DOI: https://doi.org/10.1002/chem.202302060
- [2023] Synthesis, Characterization, and Trapping of a Cyclic Diborylcarbene, an Electrophilic CarbeneDOI: https://doi.org/10.1021/jacs.3c04933
- DOI: https://doi.org/10.1016/j.polymer.2023.126116
- DOI: https://doi.org/10.1038/s41467-023-38997-2
- DOI: https://doi.org/10.1246/bcsj.20230073
- DOI: https://doi.org/10.1021/acs.organomet.3c00143
- [2023] Synthesis, Characterization, and Trapping of a Cyclic Diborylcarbene, an Electrophilic CarbeneDOI: https://doi.org/10.1021/jacs.3c04933
- DOI: https://doi.org/10.1016/j.polymer.2023.126116
- DOI: https://doi.org/10.1038/s41467-023-38997-2
- DOI: https://doi.org/10.1246/bcsj.20230073
- DOI: https://doi.org/10.1021/acs.organomet.3c00143
- DOI: https://doi.org/10.1021/acs.organomet.3c00135
- DOI: https://doi.org/10.1021/jacs.2c11145
- [2023] A dinuclear Rh(− <scp>i</scp> )/Rh( <scp>i</scp> ) complex bridged by biphilic phosphinine ligandsDOI: https://doi.org/10.1039/d3sc02292g
- DOI: https://doi.org/10.1021/acs.organomet.2c00126
- [2022] Electron in a cube: Synthesis and characterization of perfluorocubane as an electron acceptorDOI: https://doi.org/10.1126/science.abq0516
- [2022] Pincer‐Supported Perfluororhodacyclopentanes: High Nucleophilicity of the M−C<sup>F</sup> BondDOI: https://doi.org/10.1002/anie.202207760
- [2022] Pincer‐Supported Perfluororhodacyclopentanes: High Nucleophilicity of the M−C<sup>F</sup> BondDOI: https://doi.org/10.1002/ange.202207760
- DOI: https://doi.org/10.1149/ma2022-0113889mtgabs
- [2022] Pincer‐Supported Perfluororhodacyclopentanes: High Nucleophilicity of the M−C<sup>F</sup> BondDOI: https://doi.org/10.1002/anie.202207760
- [2022] Pincer‐Supported Perfluororhodacyclopentanes: High Nucleophilicity of the M−C<sup>F</sup> BondDOI: https://doi.org/10.1002/ange.202207760
- DOI: https://doi.org/10.1149/ma2022-0113889mtgabs
- DOI: https://doi.org/10.1021/acscatal.2c01974
- DOI: https://doi.org/10.1021/acs.accounts.2c00162
- DOI: https://doi.org/10.5059/yukigoseikyokaishi.80.459
- DOI: https://doi.org/10.1021/acscatal.2c01974
- DOI: https://doi.org/10.1021/acs.macromol.1c02503
- DOI: https://doi.org/10.1002/ange.202205119
- DOI: https://doi.org/10.1021/acs.accounts.2c00162
- DOI: https://doi.org/10.5059/yukigoseikyokaishi.80.459
- DOI: https://doi.org/10.1021/acs.organomet.2c00126
- DOI: https://doi.org/10.1002/ange.202205119
- DOI: https://doi.org/10.1021/acs.macromol.1c02503
- DOI: https://doi.org/10.1021/acs.organomet.2c00066
- DOI: https://doi.org/10.1002/marc.202200038
- DOI: https://doi.org/10.1002/anie.202117096
- DOI: https://doi.org/10.1002/ange.202117096
- DOI: https://doi.org/10.1021/acs.organomet.2c00037
- DOI: https://doi.org/10.1246/bcsj.20210443
- DOI: https://doi.org/10.1039/d2dt00513a
- DOI: https://doi.org/10.1002/marc.202200038
- DOI: https://doi.org/10.1002/anie.202117096
- DOI: https://doi.org/10.1002/ange.202117096
- DOI: https://doi.org/10.1021/acs.organomet.2c00037
- DOI: https://doi.org/10.1246/bcsj.20210443
- DOI: https://doi.org/10.1039/d2dt00513a
- DOI: https://doi.org/10.1021/acs.macromol.2c01761
- DOI: https://doi.org/10.1021/acs.joc.2c01302
- [2022] Electron in a cube: Synthesis and characterization of perfluorocubane as an electron acceptorDOI: https://doi.org/10.1126/science.abq0516
- DOI: https://doi.org/10.1021/acs.macromol.2c01761
- DOI: https://doi.org/10.1021/acs.joc.2c01302
- DOI: https://doi.org/10.1246/bcsj.20200402
- [2021] Single-Step Construction of Deoxypropionate Motif by Stereospecific Propylene OligomerizationDOI: https://doi.org/10.5059/yukigoseikyokaishi.79.100
- DOI: https://doi.org/10.1002/chem.202100385
- DOI: https://doi.org/10.1038/s41929-021-00598-x
- DOI: https://doi.org/10.1246/bcsj.20200402
- DOI: https://doi.org/10.1021/jacs.1c10574
- DOI: https://doi.org/10.1002/anie.202111691
- [2021] One-Pot Synthesis of Polyethylene-Based Block Copolymers <i>via</i> a Dual Polymerization PathwayDOI: https://doi.org/10.1021/jacs.1c08512
- DOI: https://doi.org/10.1021/jacs.1c08578
- DOI: https://doi.org/10.1002/anie.202110957
- DOI: https://doi.org/10.1002/ange.202110957
- [2021] Lithium Hexaphenylrhodate(III) and -Iridate(III): Structure in the Solid State and in SolutionDOI: https://doi.org/10.1021/acs.organomet.1c00248
- [2021] One-Pot Synthesis of Polyethylene-Based Block Copolymers <i>via</i> a Dual Polymerization PathwayDOI: https://doi.org/10.1021/jacs.1c08512
- DOI: https://doi.org/10.1021/jacs.1c08578
- DOI: https://doi.org/10.1002/anie.202110957
- DOI: https://doi.org/10.1021/jacs.1c10574
- [2021] Single-Step Construction of Deoxypropionate Motif by Stereospecific Propylene OligomerizationDOI: https://doi.org/10.5059/yukigoseikyokaishi.79.100
- DOI: https://doi.org/10.1002/anie.202111691
- DOI: https://doi.org/10.1002/ange.202110957
- DOI: https://doi.org/10.1002/chem.202100385
- DOI: https://doi.org/10.1021/acs.joc.1c01683
- DOI: https://doi.org/10.1002/ange.202111691
- DOI: https://doi.org/10.1002/ange.202111691
- [2021] Lithium Hexaphenylrhodate(III) and -Iridate(III): Structure in the Solid State and in SolutionDOI: https://doi.org/10.1021/acs.organomet.1c00248
- DOI: https://doi.org/10.1021/jacs.1c06714
- DOI: https://doi.org/10.1038/s41428-021-00500-3
- DOI: https://doi.org/10.1002/chem.202101499
- DOI: https://doi.org/10.1002/chem.202101499
- DOI: https://doi.org/10.1038/s41929-021-00598-x
- DOI: https://doi.org/10.1038/s41428-021-00500-3
- DOI: https://doi.org/10.1021/jacs.1c06714
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