Organic Mechanochromic Luminescent Materials with Self‐Recovering Characters

• 資料種別: 記事
• タイトル: Organic Mechanochromic Luminescent Materials with Self‐Recovering Characters
• 著者標目: Nakamura, Shotaro; Tohnai, Norimitsu; https://orcid.org/0000-0001-7051-7599; Hirano, Koji; https://orcid.org/0000-0001-9752-1985
• 出版年月日等: 2024-07-30
• 出版年（W3CDTF）: 2024-07-30
• タイトル（掲載誌）: ChemPlusChem
• 巻号年月日等（掲載誌）: 89 12
• 掲載巻: 89
• 掲載号: 12
• 掲載ページ: e202400437-1-e202400437-7
• 掲載年月日（W3CDTF）: 2024-07-30
• ISSN（掲載誌）: 21926506
• 出版事項（掲載誌）: John Wiley and Sons Inc
• 本文の言語コード: en
• 件名標目: Stimuli-responsive material; Mechanochromic luminescence; Self-recovery
• 対象利用者: 一般
• DOI: 10.1002/cplu.202400437; https://doi.org/10.1002/cplu.202400437
• オンライン閲覧公開範囲: インターネット公開
• 著作権情報: © 2024 The Authors. ChemPlusChem published by Wiley-VCH GmbH.; This article is licensed under a Creative Commons Attribution 4.0 International License.
• 関連情報（URI）: https://hdl.handle.net/11094/101967; https://chemistry-europe.onlinelibrary.wiley.com/doi/pdf/10.1002/cplu.202400437
• 参照: Direction Switching and Self‐Recovering Mechanochromic Luminescence of Anthracene‐Modified <i>o</i>‐Carboranes; https://cir.nii.ac.jp/crid/1050578847127373568; Effect of Substitution Pattern of <i>tert</i>‐Butyl Groups in a Bisbenzofuropyrazine Core π‐System on Optical Properties: Unique Mechanochromic Fluorescence Behavior; https://cir.nii.ac.jp/crid/1360004230079964672; Stimuli‐Responsive Optical Nanomaterials; https://cir.nii.ac.jp/crid/1360011143878293120; Stimuli-responsive flexible organic crystals; https://cir.nii.ac.jp/crid/1360018685021654656; Multiplexed stimuli-responsive molecules for high-security anti-counterfeiting applications; https://cir.nii.ac.jp/crid/1360025434019080960; Highly Luminescent 2D‐Type Slab Crystals Based on a Molecular Charge‐Transfer Complex as Promising Organic Light‐Emitting Transistor Materials; https://cir.nii.ac.jp/crid/1360283689375893248; Invisible Inks for Secrecy and Anticounterfeiting: From Single to Double-encryption by Hydrochromic Molecules; https://cir.nii.ac.jp/crid/1360298343158614272; Tunable mechanochromic luminescence of benzofuran-fused pyrazine: effects of alkyl chain length and branching pattern; https://cir.nii.ac.jp/crid/1360302865546876288; Self‐Recovering Mechanochromic Luminescence; https://cir.nii.ac.jp/crid/1360303275579829632; Aggregation Behavior and High Charge-Carrier OFET-Mobility of Functionalized Phenanthro[9,10-<i>d</i>]imidazoles; https://cir.nii.ac.jp/crid/1360306910697566336; An AIE-active acridine functionalized spiro[fluorene-9,9′-xanthene] luminophore with mechanoresponsive luminescence for anti-counterfeiting, information encryption and blue OLEDs; https://cir.nii.ac.jp/crid/1360306914406381952; Mechanochromic luminescence of 4-[bis(4-methylphenyl)amino]benzaldehyde; https://cir.nii.ac.jp/crid/1360567182311929088; Indolylbenzothiadiazoles with varying substituents on the indole ring: a systematic study on the self-recovering mechanochromic luminescence; https://cir.nii.ac.jp/crid/1360567183574228096; Stimuli‐Responsive Chiroptical Switching; https://cir.nii.ac.jp/crid/1360584343732642560; Light‐Responsive Luminescent Materials for Information Encryption Against Burst Force Attack; https://cir.nii.ac.jp/crid/1360588388357149952; The Role of Balancing Carrier Transport in Realizing an Efficient Orange-Red Thermally Activated Delayed-Fluorescence Organic Light-Emitting Diode; https://cir.nii.ac.jp/crid/1360588389211052416; Molecular Engineering of Triphenylamine Based Aggregation Enhanced Emissive Fluorophore: Structure-Dependent Mechanochromism and Self-Reversible Fluorescence Switching; https://cir.nii.ac.jp/crid/1360855568777916160; <i>N</i>‐Boc‐Indolylbenzothiadiazole Derivatives: Efficient Full‐Color Solid‐State Fluorescence and Self‐Recovering Mechanochromic Luminescence; https://cir.nii.ac.jp/crid/1360855570812664832; Recent advances in organic mechanofluorochromic materials; https://cir.nii.ac.jp/crid/1361137045940419456; Alkyl chain length effects on solid-state difluoroboron β-diketonate mechanochromic luminescence; https://cir.nii.ac.jp/crid/1361418520349351424; Design strategies for organic semiconductors beyond the molecular formula; https://cir.nii.ac.jp/crid/1361699995894198656; Diethylamino functionalized tetraphenylethenes: structural and electronic modulation of photophysical properties, implication for the CIE mechanism and application to cell imaging; https://cir.nii.ac.jp/crid/1361981468648480768; Modulating Mechanochromic Luminescence Quenching of Alkylated Iodo Difluoroboron Dibenzoylmethane Materials; https://cir.nii.ac.jp/crid/1361981469064260992; Tetraphenylethene-based highly emissive fluorescent molecules with aggregation-induced emission (AIE) and various mechanofluorochromic characteristics; https://cir.nii.ac.jp/crid/1361981469188914560; Reversible mechanochromic luminescence of phenothiazine-based 10,10′-bianthracene derivatives with different lengths of alkyl chains; https://cir.nii.ac.jp/crid/1362262945208107392; A carborane-triggered metastable charge transfer state leading to spontaneous recovery of mechanochromic luminescence; https://cir.nii.ac.jp/crid/1362544418736818688; From Tetraphenylfurans to Ring‐Opened (<i>Z</i>)‐1,4‐Enediones: ACQ Fluorophores versus AIEgens with Distinct Responses to Mechanical Force and Light; https://cir.nii.ac.jp/crid/1362544418830365568; Mechanofluorochromic properties of β-iminoenolate boron complexes tuned by the electronic effects of terminal phenothiazine and phenothiazine-S,S-dioxide; https://cir.nii.ac.jp/crid/1362544419954502784; Pyrene boronic acid cyclic ester: a new fast self-recovering mechanoluminescent material at room temperature; https://cir.nii.ac.jp/crid/1362544420433283968; The Relationship of Solid‐State Plasticity to Mechanochromic Luminescence in Difluoroboron Avobenzone Polymorphs; https://cir.nii.ac.jp/crid/1362825895304305920; Molecular stacking dependent phosphorescence–fluorescence dual emission in a single luminophore for self-recoverable mechanoconversion of multicolor luminescence; https://cir.nii.ac.jp/crid/1362825896182464256; Self-Reversible Mechanochromism and Thermochromism of a Triphenylamine-Based Molecule: Tunable Fluorescence and Nanofabrication Studies; https://cir.nii.ac.jp/crid/1363388843961343360; Solid-state fluorescence properties and reversible piezochromic luminescence of aggregation-induced emission-active 9,10-bis[(9,9-dialkylfluorene-2-yl)vinyl]anthracenes; https://cir.nii.ac.jp/crid/1363388844028018688; Polymorphism and Reversible Mechanochromic Luminescence for Solid-State Difluoroboron Avobenzone; https://cir.nii.ac.jp/crid/1363670319881386752; Mechanically Induced Multicolor Change of Luminescent Materials; https://cir.nii.ac.jp/crid/1363951794652497152; Recent advances in mechanochromic luminescence of organic crystalline compounds; https://cir.nii.ac.jp/crid/2051714792011533568
• 連携機関・データベース: 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• 提供元機関・データベース: 学術機関リポジトリデータベース; https://irdb.nii.ac.jp; Crossref; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja

• 記録形式（IMT）: application/pdf
• 一次資料へのリンクURL: ChemPlusChem_89_12.pdf （fulltext）; https://ir.library.osaka-u.ac.jp/repo/ouka/all/101967/ChemPlusChem_89_12.pdf
• オンライン閲覧公開範囲: インターネット公開
• 著作権情報: © 2024 The Authors. ChemPlusChem published by Wiley-VCH GmbH.; This article is licensed under a Creative Commons Attribution 4.0 International License.; https://creativecommons.org/licenses/by/4.0/
• 関連情報（DOI）: 10.1002/cplu.202400437; https://doi.org/10.1002/cplu.202400437
• 連携機関・データベース: 国立情報学研究所 : 学術機関リポジトリデータベース（IRDB）（機関リポジトリ）; https://irdb.nii.ac.jp
• 提供元機関・データベース: 大阪大学 : 大阪大学学術情報庫 桜華

• 要約等: Nakamura S., Hirano K., Tohnai N.. Organic Mechanochromic Luminescent Materials with Self-Recovering Characters. ChemPlusChem 89, e202400437 (2024); h...