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権正行助教の業績リスト

権正行助教の業績リスト

発表論文

  1. Paintable Hybrids with Thermally Stable Dual Emission Composed of Tetraphenylethene-Integrated POSS and MEH-PPV for Heat-Resistant White-Light Luminophores
  2. Controlling Energy Gaps of π-Conjugated Polymers by Multi-Fluorinated Boron-Fused Azobenzene Acceptors for Highly Efficient Near-Infrared Emission
  3. Nonmonotonic Dependence of Intramolecular Charge-Transfer Sidechain Interactions for Triazole Containing Phenylene-Ethynylene Grafted Co-Polyoxetane Brushes
  4. Facile Strategy for Obtaining Luminescent Polymorphs Based on Chirality of Boron-Fused Azomethine Complex [Outside back cover]
    • Ohtani, S.; Takeda, Y.; Gon, M.; Tanaka, K.; Chujo, Y. Chem. Commun. 2020, 56(97), 15305-15308. (DOI:10.1039/d0cc06383e)
  5. Preparation of Near-Infrared Emissive π-Conjugated Polymer Films Based on Boron-Fused Azobenzene Complexes with Perpendicularly Protruded Aryl Substituents
    • Gon, M.; Wakabayashi, J.; Nakamura, M.; Tanaka, K.; Chujo, Y. Macromol. Rapid Commun. 2020, 2000566. (DOI:10.1002/marc.202000566)
  6. Chiral lanthanide lumino-glass for a circularly polarized light security device
    • Kitagawa, Y.; Wada, S.; Islam M.D.J.; Saita, K.; Gon, M.; Fushimi, K.; Tanaka, K; Maeda, S.; Hasegawa, Y. Commun. Chem. 2020, 3, 119. (DOI:10.1038/s42004-020-00366-1)
  7. The Design Strategy for an Aggregation- and Crystallization-Induced Emission-Active Molecule Based on Introduction of Skeletal Distortion by Boron Complexation with a Tridentate Ligand
  8. Synthesis of Fully-Fused Bisboron Azomethine Complexes and Their Conjugated Polymers with Solid-State Near-Infrared Emission
    • Ohtani, S.; Nakamura, M.; Gon, M.; Tanaka, K.; Chujo, Y. Chem. Commun. 2020, 56(48), 6575-6578. (DOI:10.1039/D0CC02301A)
  9. Near-Infrared Absorptive and Emissive Poly(p-phenylene vinylene) Derivative Containing Azobenzene-Boron Complexes
  10. Enantioselective Synthesis of Triple Helicenes by Cross-Cyclotrimerization of a Helicenyl Aryne and Alkynes via Dynamic Kinetic Resolution
    • Yubuta, A.; Hosokawa, T.; Gon, M.; Tanaka, K.; Chujo, Y.; Tsurusaki, A.; Kamikawa, K. J. Am. Chem. Soc. 2020, 142(22), 10025-10033. (DOI:10.1021/jacs.0c01723) [Supplementary journal cover]
  11. Electronic strain effect on Eu(III) complexes for enhanced circularly polarized luminescence
    • Tsurui, M.; Kitagawa, Y.; Fushimi, K.; Gon, M.; Tanaka, K.; Hasegawa, Y. Dalton Trans. 2020, 49(16), 5352-5361. (DOI:10.1039/D0DT00699H)
  12. An optical sensor for discriminating the chemical compositions and sizes of plastic particles in water based on water-soluble networks consisting of polyhedral oligomeric silsesquioxane presenting dual-color luminescence
    • Nakamura, R.; Narikiyo, H.; Gon, M.; Tanaka, K.; Chujo, Y. Mater. Chem. Front. 2019, 3(12), 2690-2695. (DOI:10.1039/C9QM00510B)
  13. Near‐Infrared Circularly Polarized Luminescence through Intramolecular Excimer Formation of Oligo(p‐phenyleneethynylene)s‐Based Double Helicates
    • Miki, K.; Noda, T.; Gon, M.; Tanaka, K.; Chujo, Y.; Mizuhata, Y.; Tokitoh, N.; Ohe, K. Chem.-Eur. J. 2019, 25(39), 9211-9216. (DOI:10.1002/chem.201901467) [Front cover]
  14. Stretchable Conductive Hybrid Films Consisting of POSS-capped Polyurethane and Poly(3-hexylthiophene)
  15. Oxygen-resistant Electrochemiluminescence System with Polyhedral Oligomeric Silsesquioxane
  16. Construction of the Luminescent Donor-Acceptor Conjugated Systems Based on Boron-Fused Azomethine Acceptor
  17. Elastic and Mechanofluorochromic Hybrid Films with POSS-Capped Polyurethane and Polyfluorene
    • Gon, M.; Kato, K.; Tanaka, K.; Chujo, Y. Mater. Chem. Front. 2019, 3(6), 1174-1180. (DOI:10.1039/C9QM00100J)
  18. Unique Substitution Effect at 5,5′ Positions of a Fused Azobenzene-Boron Complex with N=N Double-Bond π-Conjugated System
  19. Preparation of Bright-Emissive Hybrid Materials Based on Light-Harvesting POSS Having Radially-Integrated Luminophores and Commercial π-Conjugated Polymers
    • Gon, M.; Sato, K.; Kato, K.; Tanaka, K.; Chujo, Y. Mater. Chem. Front. 2019, 3(2), 314-320. (DOI:10.1039/c8qm00518d)
  20. Electronic chirality inversion of lanthanide complex induced by achiral molecules
    • Wada, S.; Kitagawa, Y.; Nakanishi, T.; Gon, M., Tanaka, K.; Fushimi, K.; Chujo, Y.; Hasegawa Y. Sci. Rep. 2018, 8 16395. (DOI:10.1038/s41598-018-34790-0)
  21. Spiral Eu(III) Coordination Polymers with Circularly Polarized Luminescence
    • Hasegawa, Y.; Miura, Y.; Kitagawa, Y.; Wada, S.; Nakanishi, T.; Fushimi, K.; Seki, T.; Ito, H.; Iwasa, T.; Taketsugu, T.; Gon, M.; Tanaka, K.; Chujo, Y.; Hattori, S.; Karasawa, M.; Ishii, K. Chem. Commun. 2018, 54(76), 10695-10697. (DOI:10.1039/C8CC05147J)
  22. Synthesis of Enantiopure Planar Chiral Bis-(para)-Pseudo-meta-Type [2.2]Paracyclophanes
    • Sawada, R.; Gon, M.; Nakamura, J.; Morisaki, Y.; Chujo Y. Chirality 2018, 30(10), 1109-1114. (DOI:10.1002/chir.23010)
  23. Control of Intramolecular Excimer Emission in the Luminophores-Integrated Ionic POSS Possessing Flexible Side-Chains
    • Narikiyo, H.; Gon, M.; Tanaka, K.; Chujo, Y. Mater. Chem. Front. 2018, 2(8), 1449-1455. (DOI:10.1039/C8QM00181B)
  24. Self-assembly of [Au(CN)2]− Complexes with Tomato (Solanum Lycopersicum) Steroidal Alkaloid Glycosides to form Sheet or Tubular Structures
    • Toohara, S.; Tanaka, Y.; Sakurai, S.; Ikeda, T.; Tanaka, K.; Gon, M.; Chujo, Y.; Kuroiwa, K. Chem. Lett. 2018, 2(8), 1010-1013. (DOI:10.1246/cl.180320)
  25. Hash mark-shaped Azaacene Tetramers with Axial Chirality
    • Inoue, Y.; Sakamaki, D.; Tsutsui, Y.; Gon, M.; Chujo, Y.; Seki, S. J. Am. Chem. Soc. 2018, 140(23), 7152-7158. (DOI:10.1021/jacs.8b02689)
  26. A Highly Efficient Near‐Infrared‐Emissive Copolymer with a N=N Double‐Bond π‐Conjugated System Based on a Fused Azobenzene-Boron Complex
  27. Enhancement of aggregation-induced emission by introducing multiple o-carborane substitutions into triphenylamine
  28. A Flexible Fused Azomethine-Boron Complex: Thermochromic Luminescence and Thermosalient Behaviors in Structural Transitions between Crystalline Polymorphs
  29. A Silver(I)-Induced Higher-Ordered Structure Based on Planar Chiral Tetrasubstituted [2.2]Paracyclophane
  30. Development of Optical Sensor for Discriminating Isomers of Fatty Acids Based on Emissive Network Polymers Composed of Polyhedral Oligomeric Silsesquioxane
    • Narikiyo, H.; Kakuta, T.; Matsuyama, H.; Gon, M.; Tanaka, K; Chujo, Y. Bioorg. Med. Chem. 2017, 25(13), 3431-3436. (DOI:10.1016/j.bmc.2017.04.029)
  31. Diarylamino- and Diarylboryl-Substituted Donor-Acceptor Pyrene Derivatives: The Influence of Substitution Pattern on Their Photophysical Properties
  32. Optically Active Phenylethene Dimers Based on Planar Chiral Tetrasubstituted [2.2]Paracyclophane
  33. Enhancement and Controlling the Signal of Circularly Polarized Luminescence Based on a Planar Chiral Tetrasubstituted [2.2]Paracyclophane Framework in Aggregation System
  34. New Type of Planar Chiral [2.2]Paracyclophanes and Construction of One-Handed Double Helices
  35. Controllable Intramolecular Interaction of 3D Arranged π-Conjugated Luminophores Based on a POSS Scaffold, Leading to Highly Thermostable and Emissive Materials
  36. Optically Active Cyclic Compounds Based on Planar Chiral [2.2]Paracyclophane with Naphthalene Units
  37. Synthesis of Optically Active X-Shaped Conjugated Compounds and Dendrimers Based on Planar Chiral [2.2]Paracyclophane, Leading to Highly Emissive Circularly Polarized Luminescence
    • Gon, M.; Morisaki, Y.; Sawada, R.; Chujo, Y. Chem.-Eur. J. 2016, 22(7), 2291-2298 (DOI:10.1002/chem.201504270). [Front cover] [Hot Paper]
  38. Highly Emissive Circularly Polarized Luminescence from Optically Active Conjugated Dimers Consisting of Planar Chiral [2.2]Paracyclophane
  39. Optically Active Cyclic Compounds Based on Planar Chiral [2.2]Paracyclophane: Extension of the Conjugated Systems and Chiroptical Properties
    • Gon, M.; Morisaki, Y.; Chujo, Y. J. Mater. Chem. C 2015, 3(3), 521-529 (DOI: 10.1039/c4tc02339k). [Inside back cover]
  40. Planar Chiral Tetrasubstituted [2.2]Paracyclophane: Optical Resolution and Functionalization
    • Morisaki, Y.; Gon, M.; Sasamori, T.; Tokitoh, N.; Chujo, Y. J. Am. Chem. Soc. 2014, 136(9), 3350-3353 (DOI:10.1021/ja412197j).
  41. Conjugated Microporous Polymers Consisting of Tetrasubstituted [2.2]Paracyclophane Junctions
    • Morisaki, Y.; Gon, M.; Chujo, Y. J. Polym. Sci. Part A: Polym. Chem. 2013, 51(10), 2311-2316 (DOI:10.1002/pola.26600).
  42. Synthesis and Characterization of [2.2]Paracyclophane-containing Conjugated Microporous Polymers
    • Morisaki, Y.; Gon, M.; Tsuji, Y.; Kajiwara, Y.; Chujo, Y. Macromol. Chem. Phys. 2012, 213(5), 572-579 (DOI:10.1002/macp.201100563).
  43. Stacked 1,3,5-Tris[(2,5-dimethylphenyl)ethynyl]benzenes: Dimer and Conjugated Microporous Polymer

英語総説

  1. Discovery of Functional Luminescence Properties Based on Flexible and Bendable Boron-Fused Azomethine/Azobenzene Complexes with O,N,O-Type Tridentate Ligands
  2. Concept of Excitation-Driven Boron Complexes and Their Applications for Functional Luminescent Materials
  3. Recent Progress in the Development of Advanced Element-Block Materials
  4. Creative Synthesis of Organic-Inorganic Molecular Hybrid Materials

日本語総説

  1. 無機元素ブロックの機能模索を通じた新奇共役系高分子材料の創製
    • 権 正行,田中一生,中條善樹 高分子 2019, 68(7), 357-360.
  2. 柔軟なホウ素元素ブロックを基盤とした刺激応答性発光材料の設計
    • 田中一生,権 正行,中條善樹 日本画像学会誌 2019, 58(1), 81-92.
  3. ホウ素元素ブロックを基盤とした新奇固体発光性材料
    • 権 正行; 田中一生; 中條善樹 化学と工業, 2018, 71(4), 317−319.
  4. 元素ブロック材料研究の最近の進捗と未来展望
    • 田中一生; 権 正行; 中條善樹 化学工業 2017, 68(11), 797−803..

英語著作

  1. Molecular Designs for Solid-state Luminescent Properties and Recent Progresses on the Development of Functional Luminescent Solid Materials
    • Tanaka, K.; Gon, M.; Chujo, Y. in press.
  2. Recent Progress in the Development of Optoelectronic Materials Based on Group 13 Element-Containing Conjugated Polymers
    • Ito, S.; Gon, M.; Tanaka, K.; Chujo, Y. Conjugated Polymers, Perspective, Theory, and New Materials, Reynolds, J. R., Thompson, B. C., Skotheim, T. A. Ed., Taylor & Francis Group, 2019.
  3. Element-Block Materials: New Concept for Development of Advanced Hybrids and Inorganic Polymers
    • Gon, M.; Tanaka, K.; Chujo, Y. New Polymeric Materials Based on Element-Blocks, Chujo, Y. Ed., Springer, 2019.

日本語著作

  1. 第2章 第5節 刺激応答性元素ブロック高分子の設計と機能発現
    • 田中一生、権 正行、中條善樹 NTS出版, 刺激応答性高分子ハンドブック,宮田隆志 編著,2018.

トピックス

  • Nov. 25, 2020 当研究室の論文がChemical Communications誌でOutside back coverに選ばれました(キラル・ラセミ結晶間の発光色変化に関する研究)
  • Sep. 9, 2020 五月女君が高分子討論会パブリシティ賞を受賞しました(塗布による耐熱性白色発光ハイブリッドフィルム開発)。
  • May 14, 2020 大阪府立大学の神川先生との共同研究の論文がJACSのSupplementary Journal Coverに選ばれました。
  • Feb. 4, 2019 権正行助教が第35回井上研究奨励賞を受賞されました。
  • Dec. 20, 2018 当研究室の論文がBull. Chem. Soc. Jpn誌のinside coverに選ばれました(励起駆動型ホウ素錯体による機能性発光色素開発の総説)。
  • Apr. 16, 2018 日本化学会第98春季年会にて、権正行助教が優秀講演賞(学術)を受賞しました。
  • Jul. 06, 2017 当研究室の論文がChem. Eur. J.誌でInside coverに選ばれました(柔らかいホウ素錯体における発光クロミズム&サーモサリエント効果の発見)。
  • May. 9, 2017 当研究室の論文がChem. Eur. J.誌でBack cover pictureに選ばれました(面不斉四置換[2.2]パラシクロファン骨格を用いた光学活性フェニルエテン二量体)。
  • Sep. 20, 2016 当研究室の論文がChemistry - An Asian Journal 誌のinside coverに選出されました(新規面性不斉[2.2]パラシクロファンの合成と片巻二重らせん構築)。
  • Jun. 23, 2016 当研究室の論文がHighlights として Synfacts 誌に紹介されました(面不斉四置換[2.2]パラシクロファンをコアに有する光学活性デンドリマー)。

Optical Barrel Rolls with X-Wing Paracyclophanes Synfacts 2016, 12(5), 0472. (DOI: 10.1055/s-0035-1562014)

  • Mar. 16, 2016 当研究室の論文がAsian J. Org. Chem.誌でCover pictureに選ばれました(面不斉四置換[2.2]パラシクロファンを用いたナフタレン環含有環状化合物)。
  • Feb. 12, 2016 当研究室の論文がChem. Eur. J.誌でCover pictureに選ばれました(面不斉四置換[2.2]パラシクロファンをコアに有する光学活性デンドリマー)。
  • Feb. 12, 2016 当研究室の論文がワイリー・サイエンスカフェで紹介されました(面不斉四置換[2.2]パラシクロファンをコアに有する光学活性デンドリマー)。
  • Jan. 13, 2015 当研究室の論文がJ. Mater. Chem C誌の表紙に選ばれました(面不斉シクロファン化合物の高輝度円偏光発光)

表紙一覧

http://pubs.rsc.org/en/Content/ArticleLanding/2015/TC/C4TC02339K#!divAbstracthttp://onlinelibrary.wiley.com/wol1/doi/10.1002/chem.201504270/abstracthttp://onlinelibrary.wiley.com/doi/10.1002/ajoc.201500468/abstracthttp://onlinelibrary.wiley.com/wol1/doi/10.1002/asia.201601028/abstracthttps://doi.org/10.1002/chem.201700693http://onlinelibrary.wiley.com/doi/10.1002/chem.201703193/abstracthttps://pubs.rsc.org/en/content/articlelanding/2020/cc/d0cc06383e#!divAbstract

財団助成金(交付順)

  1. 日本化学繊維研究所
  2. 小笠原科学技術振興財団
  3. 豊田理化学研究所:平成29年度豊田理研スカラー
  4. 京都技術科学センター
  5. 有機合成化学研究所
  6. 泉科学技術振興財団
  7. 日本化学繊維研究所
  8. ポリウレタン国際技術振興財団
  9. 松籟科学技術振興財団
  10. みずほ学術振興財団
  11. 京都大学教育研究振興財団
  12. 島津科学技術振興財団
  13. 中西奨学会
  14. 稲盛財団
  15. 生研学術奨励資金