Effect of halogens in bis(haloaryloxyl)pyrazine host crystals on the room temperature phosphorescence properties of bisbenzofuropyrazine guest luminophores

• 資料種別: 記事
• タイトル: Effect of halogens in bis(haloaryloxyl)pyrazine host crystals on the room temperature phosphorescence properties of bisbenzofuropyrazine guest luminophores
• 著者・編者: Madoka Tsuboi; Shotaro Nakamura; Yuji Nishi
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2022-06-02
• 出版年（W3CDTF）: 2022-06-02
• タイトル（掲載誌）: Chemistry letters
• 巻号年月日等（掲載誌）: 51(8)
• 掲載巻: 51(8)
• ISSN（掲載誌）: 1348-0715
• ISSN-L（掲載誌）: 0366-7022
• 本文の言語コード: eng
• DOI: 10.1246/cl.220243; https://doi.org/10.1246/cl.220243
• 国立国会図書館永続的識別子: info:ndljp/pid/12998996; https://dl.ndl.go.jp/pid/12998996
• コレクション（共通）: 障害者向け資料
• コレクション（障害者向け資料：レベル1）: テキストデータ
• コレクション（個別）: 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他; https://dl.ndl.go.jp/collections/B00035
• 収集根拠: オンライン資料収集制度
• 受理日（W3CDTF）: 2023-09-27T16:20:01+09:00
• 保存日（W3CDTF）: 2023-04-26
• 記録形式（IMT）: application/pdf
• オンライン閲覧公開範囲: 国立国会図書館内限定公開
• デジタル化資料送信: 図書館・個人送信対象外
• 遠隔複写可否（NDL）: 可
• 掲載誌（URI）: https://www.journal.csj.jp/toc/cl/51/8
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/12998994; https://dl.ndl.go.jp/pid/12998994
• 連携機関・データベース: 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

• 要約等: コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
• DOI: 10.1246/cl.220243; https://doi.org/10.1246/cl.220243
• オンライン閲覧公開範囲: インターネット公開
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/12998996; https://dl.ndl.go.jp/pid/12998996; http://www.journal.csj.jp/doi/pdf/10.1246/cl.220243
• 参照: Stimuli‐Responsive Properties on a Bisbenzofuropyrazine Core: Mechanochromism and Concentration‐Controlled Vapochromism; https://cir.nii.ac.jp/crid/1050299693922870912; Tunable mechanochromic luminescence of benzofuran-fused pyrazine: effects of alkyl chain length and branching pattern; https://cir.nii.ac.jp/crid/1360302865546876288
• 参照: Recent Advances in Materials with Room‐Temperature Phosphorescence: Photophysics for Triplet Exciton Stabilization; https://cir.nii.ac.jp/crid/1360002214400316672; Recent Advancements in and the Future of Organic Emitters: TADF‐ and RTP‐Active Multifunctional Organic Materials; https://cir.nii.ac.jp/crid/1360004229947051136; 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; Wide‐Range Color‐Tunable Organic Phosphorescence Materials for Printable and Writable Security Inks; https://cir.nii.ac.jp/crid/1360011143988227584; Rational Molecular Design for Achieving Persistent and Efficient Pure Organic Room-Temperature Phosphorescence; https://cir.nii.ac.jp/crid/1360011145525559296; Siloxy Group-Induced Highly Efficient Room Temperature Phosphorescence with Long Lifetime; https://cir.nii.ac.jp/crid/1360283691586612608; Ultralong Organic Phosphorescence in the Solid State: The Case of Triphenylene Cocrystals with Halo- and Dihalo-penta/tetrafluorobenzene; https://cir.nii.ac.jp/crid/1360292620201731072; Stabilizing triplet excited states for ultralong organic phosphorescence; https://cir.nii.ac.jp/crid/1360292620303718144; Visible‐Light‐Excited Ultralong Organic Phosphorescence by Manipulating Intermolecular Interactions; https://cir.nii.ac.jp/crid/1360292620431267072; Recent Advances in Organic Light-Emitting Diodes Based on Pure Organic Room Temperature Phosphorescence Materials; https://cir.nii.ac.jp/crid/1360574095622498048; Carbazole isomers induce ultralong organic phosphorescence; https://cir.nii.ac.jp/crid/1360579819749159424; Metal‐Free Organic Luminophores that Exhibit Dual Fluorescence and Phosphorescence Emission at Room Temperature; https://cir.nii.ac.jp/crid/1360853567363927680; Tuning the Photophysical Properties of Metal-Free Room Temperature Organic Phosphors via Compositional Variations in Bromobenzaldehyde/Dibromobenzene Mixed Crystals; https://cir.nii.ac.jp/crid/1360855569986952704; Molecular Fluorescence; https://cir.nii.ac.jp/crid/1360855571383557632; Fluorescent Pigments (Daylight); https://cir.nii.ac.jp/crid/1360861294842029568; Revealing Insight into Long-Lived Room-Temperature Phosphorescence of Host–Guest Systems; https://cir.nii.ac.jp/crid/1361137045663551872; Recent advances in purely organic phosphorescent materials; https://cir.nii.ac.jp/crid/1361137046463038208; Room Temperature Phosphorescence of Metal-Free Organic Materials in Amorphous Polymer Matrices; https://cir.nii.ac.jp/crid/1361981468811959040; Solid-State Phosphorescence-to-Fluorescence Switching in a Cyclometalated Ir(III) Complex Containing an Acid-Labile Chromophoric Ancillary Ligand: Implication for Multimodal Security Printing; https://cir.nii.ac.jp/crid/1362544420413161856; Cocrystals assembled by pyrene and 1,2- or 1,4-diiodotetrafluorobenzenes and their phosphorescent behaviors modulated by local molecular environment; https://cir.nii.ac.jp/crid/1362825893323143808; Metal free room temperature phosphorescence from molecular self-interactions in the solid state; https://cir.nii.ac.jp/crid/1362825893916184704; Excited State Modulation for Organic Afterglow: Materials and Applications; https://cir.nii.ac.jp/crid/1362825895367033600; Nature of the External Heavy-Atom Effect on Radiative and Nonradiative Singlet–Triplet Transitions; https://cir.nii.ac.jp/crid/1363107368486153216; The Journey to Precious‐Metal‐Free Organic Phosphors from Single‐Benzene‐Cored Fluorophores; https://cir.nii.ac.jp/crid/1363107369342937728; Activating efficient phosphorescence from purely organic materials by crystal design; https://cir.nii.ac.jp/crid/1363107370949190144; Enhancing the performance of pure organic room-temperature phosphorescent luminophores; https://cir.nii.ac.jp/crid/1363107371247694976; Recent Advances in Polymer‐Based Metal‐Free Room‐Temperature Phosphorescent Materials; https://cir.nii.ac.jp/crid/1363388846160285696; Biluminescence via Fluorescence and Persistent Phosphorescence in Amorphous Organic Donor(D₄)–Acceptor(A) Conjugates and Application in Data Security Protection; https://cir.nii.ac.jp/crid/1363670318735438592; Design of Phosphorescent Organic Molecules: Old Concepts under a New Light; https://cir.nii.ac.jp/crid/1363670319445987840; Room‐Temperature Phosphorescence in Metal‐Free Organic Materials; https://cir.nii.ac.jp/crid/1363670320236979200; Organic Room Temperature Phosphorescence Materials for Biomedical Applications; https://cir.nii.ac.jp/crid/1363670320898306560; Room-temperature phosphorescence of polynuclear aromatic hydrocarbons in cyclodextrins; https://cir.nii.ac.jp/crid/1363951793296558080; Rigidification or interaction-induced phosphorescence of organic molecules; https://cir.nii.ac.jp/crid/1363951794449790208; Recent Progress in Phosphorescent Organic Light‐Emitting Devices; https://cir.nii.ac.jp/crid/1364233269447260800; Induction of Strong Long‐Lived Room‐Temperature Phosphorescence of <i>N</i>‐Phenyl‐2‐naphthylamine Molecules by Confinement in a Crystalline Dibromobiphenyl Matrix; https://cir.nii.ac.jp/crid/1364233269840043392; Room-temperature phosphorescence from organic aggregates; https://cir.nii.ac.jp/crid/1364233269995123456; Intersystem Crossing Mechanisms in the Room Temperature Phosphorescence of Crystalline Organic Compounds; https://cir.nii.ac.jp/crid/1523388079768977408; Syntheses and room temperature phosphorescence properties of dibenzobenzodithiophenes and dibenzothiophenes; https://cir.nii.ac.jp/crid/2050307417131923968; Room temperature phosphorescent crystals consisting of cyclized guests and their uncyclized mother host molecules; https://cir.nii.ac.jp/crid/2051433317032479360; Tellurophenes and their emergence as building blocks for polymeric and light-emitting materials; https://cir.nii.ac.jp/crid/2051996266974997248
• 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: 雑誌記事索引データベース; https://ndlsearch.ndl.go.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
• 書誌ID（NDLBibID）: 12998996; http://id.ndl.go.jp/bib/12998996