Synthesis of trioxotriangulene stable neutral π-radicals having alkyl substituent groups, and their effects on electronic-spin and π-stacking structures

• 資料種別: 記事
• タイトル: Synthesis of trioxotriangulene stable neutral π-radicals having alkyl substituent groups, and their effects on electronic-spin and π-stacking structures
• 著者・編者: Tsuyoshi Murata; Masaaki Yokoyama; Akira Ueda
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2019-11-21
• 出版年（W3CDTF）: 2019-11-21
• タイトル（掲載誌）: Chemistry letters
• 巻号年月日等（掲載誌）: 49(1)
• 掲載巻: 49(1)
• 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.190761; https://doi.org/10.1246/cl.190761
• 国立国会図書館永続的識別子: info:ndljp/pid/11676860; https://dl.ndl.go.jp/pid/11676860
• 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 > 学術機関 > 学協会; https://dl.ndl.go.jp/collections/B00043
• 収集根拠: オンライン資料収集制度
• 受理日（W3CDTF）: 2021-06-01T10:30:27+09:00
• 保存日（W3CDTF）: 2020-04-27
• 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/49/1
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/11676853; https://dl.ndl.go.jp/pid/11676853
• 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 > 学術機関 > 学協会
• DOI: 10.1246/cl.190761; https://doi.org/10.1246/cl.190761
• オンライン閲覧公開範囲: インターネット公開
• 関連情報: CCDC 1965084: Experimental Crystal Structure Determination; https://cir.nii.ac.jp/crid/1882553967499198464
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/11676860; https://dl.ndl.go.jp/pid/11676860; http://www.journal.csj.jp/doi/pdf/10.1246/cl.190761
• 参照: Double‐σ‐Bonded Close‐Shell Dimers and Peroxy‐Linked Open‐Shell Dimer Derived from a <i>C</i>₃ Symmetric Trioxophenalenyl Neutral Diradical; https://cir.nii.ac.jp/crid/1360017282200401920; High Capacity and Energy Density Organic Lithium‐Ion Battery Based on Buckypaper with Stable π‐Radical; https://cir.nii.ac.jp/crid/1360290617719505152; 2D Coordination Network of Trioxotriangulene with Multiple Redox Abilities and Its Rechargeable Battery Performance; https://cir.nii.ac.jp/crid/1360290617721004288; A Redox‐Active Microporous Organosiloxane Containing a Stable Neutral Radical, Trioxotriangulene; https://cir.nii.ac.jp/crid/1360294643821185792; Synthesis and Physical Properties of Trioxotriangulene Having Methoxy and Hydroxy Groups at α-Positions: Electronic and Steric Effects of Substituent Groups and Intramolecular Hydrogen Bonds; https://cir.nii.ac.jp/crid/1360294643821916928; Cold Crystallization and Polymorphism Triggered by the Mobility of the Phenyl Group in Alkyl Azo Dye Molecules; https://cir.nii.ac.jp/crid/1360295658376623616; Issues on DFT+<i>U</i> calculations of organic diradicals; https://cir.nii.ac.jp/crid/1360302864801271424; Spin–spin interaction in a highly stable neutral diradical: σ-boned dimer of trioxotriangulene; https://cir.nii.ac.jp/crid/1360302865557526528; π‐Expansion on a Polycyclic Stable Neutral Radical: Synthesis and Physical Properties of a Benz‐Annulated Trioxotriangulene; https://cir.nii.ac.jp/crid/1360306906065838336; Rechargeable Batteries with 100% Cathode Active Materials─Conductive Vapor-Deposited Films of a Stable Organic Neutral Radical; https://cir.nii.ac.jp/crid/1360576118797072384
• 参照: Organic tailored batteries materials using stable open-shell molecules with degenerate frontier orbitals; https://cir.nii.ac.jp/crid/1360002216809180288; Colored Ionic Liquid Based on Stable Polycyclic Anion Salt Showing Halochromism with HCl Vapor; https://cir.nii.ac.jp/crid/1360004233142860160; Near-infrared absorption of π-stacking columns composed of trioxotriangulene neutral radicals; https://cir.nii.ac.jp/crid/1360004233471081344; Mixed valence salts based on carbon-centered neutral radical crystals; https://cir.nii.ac.jp/crid/1360004233498881024; The First Electronically Stabilized Phenalenyl Radical: Effect of Substituents on Solution Chemistry and Solid-State Structure; https://cir.nii.ac.jp/crid/1360011144308186368; Perchlorophenalenyl Radical; https://cir.nii.ac.jp/crid/1360011145224680320; Pancake Bonding: An Unusual Pi‐Stacking Interaction; https://cir.nii.ac.jp/crid/1360011145754154496; Atomically precise bottom-up synthesis of π-extended [5]triangulene; https://cir.nii.ac.jp/crid/1360011146139997824; Intramolecular Magnetic Interaction of Spin‐Delocalized Neutral Radicals through <i>m</i>‐Phenylene Spacers; https://cir.nii.ac.jp/crid/1360285705055418112; Pancake Bond Orders of a Series of π‐Stacked Triangulene Radicals; https://cir.nii.ac.jp/crid/1360292618866647680; Biphenalenylidene: Isolation and Characterization of the Reactive Intermediate on the Decomposition Pathway of Phenalenyl Radical; https://cir.nii.ac.jp/crid/1360565166613475712; Platforms for Stable Carbon‐Centered Radicals; https://cir.nii.ac.jp/crid/1360567179880153600; A NEW AND SELECTIVE METHOD OF OXIDATION. THE CONVERSION OF ALKYL HALIDES AND ALKYL TOSYLATES TO ALDEHYDES; https://cir.nii.ac.jp/crid/1360574093763815936; Resonating Valence Bond Ground State in Oxygen-Functionalized Phenalenyl-Based Neutral Radical Molecular Conductors; https://cir.nii.ac.jp/crid/1360574095160655104; A Stable Neutral Hydrocarbon Radical: Synthesis, Crystal Structure, and Physical Properties of 2,5,8-Tri-<i>tert</i>-butyl-phenalenyl; https://cir.nii.ac.jp/crid/1360574096342188544; Donor–Acceptor Molecular Triangles; https://cir.nii.ac.jp/crid/1360574096536432768; Evidence of σ- and π-Dimerization in a Series of Phenalenyls; https://cir.nii.ac.jp/crid/1360846641589013632; Synthetic organic spin chemistry for structurally well-defined open-shell graphene fragments; https://cir.nii.ac.jp/crid/1360846641731509888; Dual Association Modes of the 2,5,8‐Tris(pentafluorophenyl)phenalenyl Radical; https://cir.nii.ac.jp/crid/1360848654875635840; Metal-free electrocatalysts for oxygen reduction reaction based on trioxotriangulene; https://cir.nii.ac.jp/crid/1360848658429095680; Encyclopedia of Radicals in Chemistry, Biology and Materials; https://cir.nii.ac.jp/crid/1360855569331271936; Quantum chemical studies in the design of organic metals. III. Odd-alternant hydrocarbons–The phenalenyl (ply) system; https://cir.nii.ac.jp/crid/1360855569647171712; Light-Mediated C−C σ-Bond Driven Crystallization of a Phenalenyl Radical Dimer; https://cir.nii.ac.jp/crid/1360855570296089472; Emergence of an Antiferromagnetic Mott Insulating Phase in Hexagonal π‐Conjugated Covalent Organic Frameworks; https://cir.nii.ac.jp/crid/1361137044080055168; The Chloromethylation of 5-Nitrosalicylaldehyde; https://cir.nii.ac.jp/crid/1361137046421289984; Synthesis of a derivative of triangulene; the first non-kekulé polynuclear aromatic; https://cir.nii.ac.jp/crid/1361418518719094272; Gram-Scale Synthesis and Supramolecular Complex of Precursors of Clar’s Hydrocarbon Triangulene; https://cir.nii.ac.jp/crid/1361418519050462592; Trioxotriangulene with carbazole: a donor–acceptor molecule showing strong near-infrared absorption exceeding 1000 nm; https://cir.nii.ac.jp/crid/1361418520516005632; The First Phenalenyl-Based Neutral Radical Molecular Conductor; https://cir.nii.ac.jp/crid/1361699994500071040; Aromaticity on the Pancake-Bonded Dimer of Neutral Phenalenyl Radical as Studied by MS and NMR Spectroscopies and NICS Analysis; https://cir.nii.ac.jp/crid/1361981468457317504; Synthesis and Characterization of π-Extended Triangulene; https://cir.nii.ac.jp/crid/1361981470353753856; Syntheses of syn-[2.2]metacyclophanes and triple-layered anti-[2.2]metacyclophanes; https://cir.nii.ac.jp/crid/1362262943737963520; Synthesis and characterization of triangulene; https://cir.nii.ac.jp/crid/1362544419344491136; Stable Radicals; https://cir.nii.ac.jp/crid/1362544420322015104; Air-Stable Thin Films with High and Anisotropic Electrical Conductivities Composed of a Carbon-Centered Neutral π-Radical; https://cir.nii.ac.jp/crid/1362825893909586560; Phenalenyl-Based Neutral Radical Molecular Conductors: Substituent Effects on Solid-State Structures and Properties; https://cir.nii.ac.jp/crid/1362825893943302912; Thermochromism in an organic crystal based on the coexistence of σ- and π-dimers; https://cir.nii.ac.jp/crid/1363107369891806592; Resonating Valence-Bond Ground State in a Phenalenyl-Based Neutral Radical Conductor; https://cir.nii.ac.jp/crid/1363388843358255488; Phenalenyls, Cyclopentadienyls, and Other Carbon‐Centered Radicals; https://cir.nii.ac.jp/crid/1363388843886614272; 520. The chemistry of the triterpenes and related compounds. Part XVIII. Elucidation of the structure of polyporenic acid C; https://cir.nii.ac.jp/crid/1363388845913462400; Air‐Stable Redox‐Active Neutral Radicals; https://cir.nii.ac.jp/crid/1363670318859383424; What's new in stable radical chemistry?; https://cir.nii.ac.jp/crid/1363951795756086528; Magneto-Opto-Electronic Bistability in a Phenalenyl-Based Neutral Radical; https://cir.nii.ac.jp/crid/1363951796241511936; Dimeric Phenalenyl-Based Neutral Radical Molecular Conductors; https://cir.nii.ac.jp/crid/1364233270802303360; Trioxotriangulene : air- and thermally stable organic carbon-centered neutral π-radical without steric protection; https://cir.nii.ac.jp/crid/2050307417114719488
• 参照（URI）: https://cir.nii.ac.jp/crid/1370007980114986512
• 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; CiNii Articles
• 書誌ID（NDLBibID）: 11676860; http://id.ndl.go.jp/bib/11676860
• NII論文ID: 130007782550