Synthesis of trioxotriangulene stable neutral π-radicals having alkyl substituent groups, and their effects on electronic-spin and π-stacking structures
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DOI[10.1246/cl.190761]to the data of the same series
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- Material Type
- 記事
- Author/Editor
- Tsuyoshi MurataMasaaki YokoyamaAkira Ueda
- Publication, Distribution, etc.
- Publication Date
- 2019-11-21
- Publication Date (W3CDTF)
- 2019-11-21
- Periodical title
- Chemistry letters
- No. or year of volume/issue
- 49(1)
- Volume
- 49(1)
- ISSN (Periodical Title)
- 1348-0715
- ISSN-L (Periodical Title)
- 0366-7022
- Text Language Code
- eng
- DOI
- 10.1246/cl.190761
- Persistent ID (NDL)
- info:ndljp/pid/11676860
- Collection
- Collection (Materials For Handicapped People:1)
- Collection (particular)
- 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
- Acquisition Basis
- オンライン資料収集制度
- Date Accepted (W3CDTF)
- 2021-06-01T10:30:27+09:00
- Date Captured (W3CDTF)
- 2020-04-27
- Format (IMT)
- application/pdf
- Access Restrictions
- 国立国会図書館内限定公開
- Service for the Digitized Contents Transmission Service
- 図書館・個人送信対象外
- Availability of remote photoduplication service
- 可
- Periodical Title (URI)
- Periodical Title (Persistent ID (NDL))
- info:ndljp/pid/11676853
- Data Provider (Database)
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- Summary, etc.
- 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
- Access Restrictions
- インターネット公開
- Related Material
- CCDC 1965084: Experimental Crystal Structure Determination
- Related Material (URI)
- Is Referenced By
- Double‐σ‐Bonded Close‐Shell Dimers and Peroxy‐Linked Open‐Shell Dimer Derived from a <i>C</i><sub>3</sub> Symmetric Trioxophenalenyl Neutral DiradicalHigh Capacity and Energy Density Organic Lithium‐Ion Battery Based on Buckypaper with Stable π‐Radical2D Coordination Network of Trioxotriangulene with Multiple Redox Abilities and Its Rechargeable Battery PerformanceA Redox‐Active Microporous Organosiloxane Containing a Stable Neutral Radical, TrioxotrianguleneSynthesis and Physical Properties of Trioxotriangulene Having Methoxy and Hydroxy Groups at α-Positions: Electronic and Steric Effects of Substituent Groups and Intramolecular Hydrogen BondsCold Crystallization and Polymorphism Triggered by the Mobility of the Phenyl Group in Alkyl Azo Dye MoleculesIssues on DFT+<i>U</i> calculations of organic diradicalsSpin–spin interaction in a highly stable neutral diradical: σ-boned dimer of trioxotrianguleneπ‐Expansion on a Polycyclic Stable Neutral Radical: Synthesis and Physical Properties of a Benz‐Annulated TrioxotrianguleneRechargeable Batteries with 100% Cathode Active Materials─Conductive Vapor-Deposited Films of a Stable Organic Neutral Radical
- References
- Organic tailored batteries materials using stable open-shell molecules with degenerate frontier orbitalsColored Ionic Liquid Based on Stable Polycyclic Anion Salt Showing Halochromism with HCl VaporNear-infrared absorption of π-stacking columns composed of trioxotriangulene neutral radicalsMixed valence salts based on carbon-centered neutral radical crystalsThe First Electronically Stabilized Phenalenyl Radical: Effect of Substituents on Solution Chemistry and Solid-State StructurePerchlorophenalenyl RadicalPancake Bonding: An Unusual Pi‐Stacking InteractionAtomically precise bottom-up synthesis of π-extended [5]trianguleneIntramolecular Magnetic Interaction of Spin‐Delocalized Neutral Radicals through <i>m</i>‐Phenylene SpacersPancake Bond Orders of a Series of π‐Stacked Triangulene RadicalsBiphenalenylidene: Isolation and Characterization of the Reactive Intermediate on the Decomposition Pathway of Phenalenyl RadicalPlatforms for Stable Carbon‐Centered RadicalsA NEW AND SELECTIVE METHOD OF OXIDATION. THE CONVERSION OF ALKYL HALIDES AND ALKYL TOSYLATES TO ALDEHYDESResonating Valence Bond Ground State in Oxygen-Functionalized Phenalenyl-Based Neutral Radical Molecular ConductorsA Stable Neutral Hydrocarbon Radical: Synthesis, Crystal Structure, and Physical Properties of 2,5,8-Tri-<i>tert</i>-butyl-phenalenylDonor–Acceptor Molecular TrianglesEvidence of σ- and π-Dimerization in a Series of PhenalenylsSynthetic organic spin chemistry for structurally well-defined open-shell graphene fragmentsDual Association Modes of the 2,5,8‐Tris(pentafluorophenyl)phenalenyl RadicalMetal-free electrocatalysts for oxygen reduction reaction based on trioxotrianguleneEncyclopedia of Radicals in Chemistry, Biology and MaterialsQuantum chemical studies in the design of organic metals. III. Odd-alternant hydrocarbons–The phenalenyl (ply) systemLight-Mediated C−C σ-Bond Driven Crystallization of a Phenalenyl Radical DimerEmergence of an Antiferromagnetic Mott Insulating Phase in Hexagonal π‐Conjugated Covalent Organic FrameworksThe Chloromethylation of 5-NitrosalicylaldehydeSynthesis of a derivative of triangulene; the first non-kekulé polynuclear aromaticGram-Scale Synthesis and Supramolecular Complex of Precursors of Clar’s Hydrocarbon TrianguleneTrioxotriangulene with carbazole: a donor–acceptor molecule showing strong near-infrared absorption exceeding 1000 nmThe First Phenalenyl-Based Neutral Radical Molecular ConductorAromaticity on the Pancake-Bonded Dimer of Neutral Phenalenyl Radical as Studied by MS and NMR Spectroscopies and NICS AnalysisSynthesis and Characterization of π-Extended TrianguleneSyntheses of syn-[2.2]metacyclophanes and triple-layered anti-[2.2]metacyclophanesSynthesis and characterization of trianguleneStable RadicalsAir-Stable Thin Films with High and Anisotropic Electrical Conductivities Composed of a Carbon-Centered Neutral π-RadicalPhenalenyl-Based Neutral Radical Molecular Conductors: Substituent Effects on Solid-State Structures and PropertiesThermochromism in an organic crystal based on the coexistence of σ- and π-dimersResonating Valence-Bond Ground State in a Phenalenyl-Based Neutral Radical ConductorPhenalenyls, Cyclopentadienyls, and Other Carbon‐Centered Radicals520. The chemistry of the triterpenes and related compounds. Part XVIII. Elucidation of the structure of polyporenic acid CAir‐Stable Redox‐Active Neutral RadicalsWhat's new in stable radical chemistry?Magneto-Opto-Electronic Bistability in a Phenalenyl-Based Neutral RadicalDimeric Phenalenyl-Based Neutral Radical Molecular ConductorsTrioxotriangulene : air- and thermally stable organic carbon-centered neutral π-radical without steric protection
- References (URI)
- Data Provider (Database)
- 国立情報学研究所 : CiNii Research
- Original Data Provider (Database)
- 雑誌記事索引データベースCrossrefCiNii ArticlesCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossref
- Bibliographic ID (NDL)
- 11676860
- NAID
- 130007782550