Fourfold C-H borylation of anthracene : 1,3,5,7-tetraborylanthracene and its application to 1,3,5,7-tetraarylanthracenes

• 資料種別: 記事
• タイトル: Fourfold C-H borylation of anthracene : 1,3,5,7-tetraborylanthracene and its application to 1,3,5,7-tetraarylanthracenes
• 著者・編者: Yuta Takaki; Kenji Yoza; Kenji Kobayashi
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2017-02-16
• 出版年（W3CDTF）: 2017-02-16
• タイトル（掲載誌）: Chemistry letters
• 巻号年月日等（掲載誌）: 46(5)
• 掲載巻: 46(5)
• 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.170037; https://doi.org/10.1246/cl.170037
• 国立国会図書館永続的識別子: info:ndljp/pid/11478000; https://dl.ndl.go.jp/pid/11478000
• 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）: 2020-04-02T20:54:50+09:00
• 保存日（W3CDTF）: 2020-04-02
• 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/46/5
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/11477997; https://dl.ndl.go.jp/pid/11477997
• 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.170037; https://doi.org/10.1246/cl.170037
• 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 1525353: Experimental Crystal Structure Determination; https://cir.nii.ac.jp/crid/1882553967666355200
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/11478000; https://dl.ndl.go.jp/pid/11478000; https://www.journal.csj.jp/doi/pdf/10.1246/cl.170037
• 参照: Straightforward and regiospecific synthesis of 1,3,5,7-tetra-arylated acene bearing different aryl groups; https://cir.nii.ac.jp/crid/1050578083321189248; Synthesis and Properties of a Cyclohexa‐2,7‐anthrylene Ethynylene Derivative; https://cir.nii.ac.jp/crid/1051130853467871616; Functionalization of Azapentabenzocorannulenes by Fivefold C−H Borylation and Cross‐Coupling Arylation: Application to Columnar Liquid‐Crystalline Materials; https://cir.nii.ac.jp/crid/1360004229996535424
• 参照: Double Alkylene-Strapped Diphenylanthracene as a Photostable and Intense Solid-State Blue-Emitting Material; https://cir.nii.ac.jp/crid/1360002216668855040; Soluble 2,6-Bis(4-pentylphenylethynyl)anthracene as a High Hole Mobility Semiconductor for Organic Field-effect Transistors; https://cir.nii.ac.jp/crid/1360002219105845504; A Macrocyclic Fluorophore Dimer with Flexible Linkers: Bright Excimer Emission with a Long Fluorescence Lifetime; https://cir.nii.ac.jp/crid/1360004229923202432; Disilanyl Double‐Pillared Bisanthracene: A Bipolar Carrier Transport Material for Organic Light‐Emitting Diode Devices; https://cir.nii.ac.jp/crid/1360285704893245056; Catalytic Functionalization of Methyl Group on Silicon: Iridium-Catalyzed C(sp³)–H Borylation of Methylchlorosilanes; https://cir.nii.ac.jp/crid/1360565166611931136; Donor−Acceptor-Substituted Anthracene-Centered Cruciforms: Synthesis, Enhanced Two-Photon Absorptions, and Spatially Separated Frontier Molecular Orbitals; https://cir.nii.ac.jp/crid/1360574095460925440; Engineering Stacks of V‐Shaped Polyaromatic Compounds with Alkyl Chains for Enhanced Emission in the Solid State; https://cir.nii.ac.jp/crid/1360846639355518848; Photon Upconversion in Supramolecular Gel Matrixes: Spontaneous Accumulation of Light-Harvesting Donor–Acceptor Arrays in Nanofibers and Acquired Air Stability; https://cir.nii.ac.jp/crid/1360846641589034112; 2,7-Diborylanthracene as a Useful Building Block for Extended π-Conjugated Aromatics; https://cir.nii.ac.jp/crid/1360846644041723904; The first soluble conjugated poly(2,6-anthrylene): synthesis and properties; https://cir.nii.ac.jp/crid/1360855571053856768; Semiconducting 2,6,9,10-Tetrakis(phenylethynyl)anthracene Derivatives: Effect of Substitution Positions on Molecular Energies; https://cir.nii.ac.jp/crid/1361137043839099392; High‐Performance Organic Single‐Crystal Transistors and Digital Inverters of an Anthracene Derivative; https://cir.nii.ac.jp/crid/1361137045139867392; Excimer-induced high-efficiency fluorescence due to pairwise anthracene stacking in a crystal with long lifetime; https://cir.nii.ac.jp/crid/1361137046435650048; Iridium-Catalyzed Borylation of Pyrene: Irreversibility and the Influence of Ligand on Selectivity; https://cir.nii.ac.jp/crid/1361418519754555264; Facile Synthetic Approach to a Large Variety of Soluble Diarenoperylenes; https://cir.nii.ac.jp/crid/1361418521211300864; 2,8- and 2,9-Diboryltetracenes as Useful Building Blocks for Extended π-Conjugated Tetracenes; https://cir.nii.ac.jp/crid/1361699994220022784; Pushing the Ir-Catalyzed C–H Polyborylation of Aromatic Compounds to Maximum Capacity by Exploiting Reversibility; https://cir.nii.ac.jp/crid/1361699995458824448; Convenient Synthesis of Tetra- and Hexaarylanthracenes by Means of RuH₂(CO)(PPh₃)₃-Catalyzed C−H Arylation of Anthraquinone with Arylboronates; https://cir.nii.ac.jp/crid/1361699996215426688; Iridium-Catalyzed Borylation of Secondary C–H Bonds in Cyclic Ethers; https://cir.nii.ac.jp/crid/1361981469721338496; Metal‐Catalyzed Cross‐Coupling Reactions and More; https://cir.nii.ac.jp/crid/1362262946225326720; Catalysts for Suzuki−Miyaura Coupling Processes: Scope and Studies of the Effect of Ligand Structure; https://cir.nii.ac.jp/crid/1362262946271033984; A General Method for Growing Two‐Dimensional Crystals of Organic Semiconductors by “Solution Epitaxy”; https://cir.nii.ac.jp/crid/1362825896408616832; High-Throughput Optimization of Ir-Catalyzed C–H Borylation: A Tutorial for Practical Applications; https://cir.nii.ac.jp/crid/1363107368567642112; Selective Ir-catalysed borylation of polycyclic aromatic hydrocarbons: structures of naphthalene-2,6-bis(boronate), pyrene-2,7-bis(boronate) and perylene-2,5,8,11-tetra(boronate) esters; https://cir.nii.ac.jp/crid/1363107370049497600; Mild Iridium-Catalyzed Borylation of Arenes. High Turnover Numbers, Room Temperature Reactions, and Isolation of a Potential Intermediate; https://cir.nii.ac.jp/crid/1363670319855040000; C−H Activation for the Construction of C−B Bonds; https://cir.nii.ac.jp/crid/1364233269500734976
• 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）: 11478000; http://id.ndl.go.jp/bib/11478000
• NII論文ID: 130005655631