Synthesis, properties, and intermolecular interactions in the solid states of π-congested X-shaped 1,2,4,5-tetra(9-anthryl)benzenes

• 資料種別: 記事
• タイトル: Synthesis, properties, and intermolecular interactions in the solid states of π-congested X-shaped 1,2,4,5-tetra(9-anthryl)benzenes
• 著者・編者: Tomohiko Nishiuchi; Shino Takeuchi; Yuta Makihara
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2022-10-07
• 出版年（W3CDTF）: 2022-10-07
• タイトル（掲載誌）: Bulletin of the Chemical Society of Japan
• 巻号年月日等（掲載誌）: 95(11)
• 掲載巻: 95(11)
• ISSN（掲載誌）: 1348-0634
• ISSN-L（掲載誌）: 0009-2673
• 本文の言語コード: eng
• DOI: 10.1246/bcsj.20220257; https://doi.org/10.1246/bcsj.20220257
• 国立国会図書館永続的識別子: info:ndljp/pid/12686462; https://dl.ndl.go.jp/pid/12686462
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• 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）: 2023-03-07T17:43:09+09:00
• 保存日（W3CDTF）: 2023-01-20
• 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/bcsj/95/11
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/12686459; https://dl.ndl.go.jp/pid/12686459
• 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/bcsj.20220257; https://doi.org/10.1246/bcsj.20220257; 10.26434/chemrxiv-2022-5fdnf-v2; https://doi.org/10.26434/chemrxiv-2022-5fdnf-v2; 10.26434/chemrxiv-2022-5fdnf; https://doi.org/10.26434/chemrxiv-2022-5fdnf
• 関連情報: CCDC 2157952: Experimental Crystal Structure Determination; https://cir.nii.ac.jp/crid/1880020692745228032; CCDC 2192879: Experimental Crystal Structure Determination; https://cir.nii.ac.jp/crid/1880302167858914944; CCDC 2195284: Experimental Crystal Structure Determination; https://cir.nii.ac.jp/crid/1880865117753291904; CCDC 2195283: Experimental Crystal Structure Determination; https://cir.nii.ac.jp/crid/1880865118303398784; CCDC 2157951: Experimental Crystal Structure Determination; https://cir.nii.ac.jp/crid/1882835442859128064; CCDC 2157953: Experimental Crystal Structure Determination; https://cir.nii.ac.jp/crid/1883398392424845696
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/12686462; https://dl.ndl.go.jp/pid/12686462; https://chemrxiv.org/engage/api-gateway/chemrxiv/assets/orp/resource/item/6336cf2a0e3c6ac4782e5236/original/synthesis-properties-and-intermolecular-interactions-in-the-solid-states-of-p-congested-x-shaped-1-2-4-5-tetra-9-anthryl-benzenes.pdf; https://academic.oup.com/bcsj/article-pdf/95/11/1591/56315390/bcsj.20220257.pdf
• 参照: Donor-only substituted benzene achieves thermally activated delayed fluorescence; https://cir.nii.ac.jp/crid/1050020596872779008; Hexacarbazolylbenzene: An Excellent Host Molecule Causing Strong Guest Molecular Orientation and the High‐Performance OLEDs; https://cir.nii.ac.jp/crid/1050024953984421248; Recent Advancements in Novel Sensing Systems through Nanoarchitectonics; https://cir.nii.ac.jp/crid/1360021390564221952; Conjugated photothermal materials and structure design for solar steam generation; https://cir.nii.ac.jp/crid/1360298757177509120; Bis‐<i>Ortho</i>‐Donor‐Modification of Boracyclic π‐Electron Systems beyond Steric Protection to Produce Thermally Activated Delayed Fluorescence Materials; https://cir.nii.ac.jp/crid/1360306905148921088; Long carbon–carbon bonds and beyond; https://cir.nii.ac.jp/crid/1360306906073516160; Using an aromatic linker to optimize charge-resonance states, photodimerization and reversibility in covalent anthracene dimers; https://cir.nii.ac.jp/crid/1360869855561460864
• 参照: Longest C–C Single Bond among Neutral Hydrocarbons with a Bond Length beyond1.8Å; https://cir.nii.ac.jp/crid/1050025031475977088; Synthesis and Properties of a Highly Congested Tri(9‐anthryl)methyl Radical; https://cir.nii.ac.jp/crid/1360004229926540032; Box-shaped Cyclic Oligoarenes: Synthesis and Structure of Anthracene-1,8-diyl Cyclic Tetramers; https://cir.nii.ac.jp/crid/1360004237005090816; 727. Bi(anthracene-9,10-dimethylene)(tetrabenzo-[2,2]-paracyclophane]; https://cir.nii.ac.jp/crid/1360011143795604096; Discovery of a Neutral-to-Ionic Phase Transition in Organic Materials; https://cir.nii.ac.jp/crid/1360011145930247808; Synthesis, properties and chemical modification of a persistent triisopropylsilylethynyl substituted tri(9-anthryl)methyl radical; https://cir.nii.ac.jp/crid/1360013168730674944; Sterically Frustrated Aromatic Enes with Various Colors Originating from Multiple Folded and Twisted Conformations in Crystal Polymorphs**; https://cir.nii.ac.jp/crid/1360016864727099776; Exciplex Stabilization in Asymmetric Acene Dimers; https://cir.nii.ac.jp/crid/1360016868484028672; Syntheses and Structures of 10‐Trimethylelement‐Substituted 1,8‐Dichloroanthracenes; https://cir.nii.ac.jp/crid/1360016869558485888; Stacked antiaromaticity in the π‐congested space between the aromatic rings in the anthracene dimer; https://cir.nii.ac.jp/crid/1360016870029390080; Recent Advances on Host–Guest Material Systems toward Organic Room Temperature Phosphorescence; https://cir.nii.ac.jp/crid/1360016870034935680; Optical Nature of Non-Substituted Triphenylmethyl Cation: Crystalline State Emission, Thermochromism, and Phosphorescence; https://cir.nii.ac.jp/crid/1360022304973789696; Synthesis of π-Extended Thiele's and Chichibabin's Hydrocarbons and Effect of the π-congestion on Conformations and Electronic States; https://cir.nii.ac.jp/crid/1360022306717801728; Ultrapure Blue Thermally Activated Delayed Fluorescence Molecules: Efficient HOMO–LUMO Separation by the Multiple Resonance Effect; https://cir.nii.ac.jp/crid/1360283689375609856; Photodimerization of benzenes in strained dihetera[3.3]metacyclophanes; https://cir.nii.ac.jp/crid/1360292620087789568; Synthesis of Anthracene‐Based Cyclic π‐Clusters and Elucidation of their Properties Originating from Congested Aromatic Planes; https://cir.nii.ac.jp/crid/1360572092657918848; Triplet-singlet emission in fluid solutions. Phosphorescence of eosin; https://cir.nii.ac.jp/crid/1360574093656849408; Recent advances in organic thermally activated delayed fluorescence materials; https://cir.nii.ac.jp/crid/1360574094716610304; Highly efficient organic light-emitting diodes from delayed fluorescence; https://cir.nii.ac.jp/crid/1360574094804964736; Cyclophane chemistry: bent and battered benzene rings; https://cir.nii.ac.jp/crid/1360574094853587328; Recent progress on organic exciplex materials with different donor–acceptor contacting modes for luminescent applications; https://cir.nii.ac.jp/crid/1360579820500305408; A Calix[3]acridan‐Based Host–Guest Cocrystal Exhibiting Efficient Thermally Activated Delayed Fluorescence; https://cir.nii.ac.jp/crid/1360580236807001856; Efficient up-conversion of triplet excitons into a singlet state and its application for organic light emitting diodes; https://cir.nii.ac.jp/crid/1360845538917171712; Intramolecular Interaction, Photoisomerization, and Mechanical C–C Bond Dissociation of 1,2-Di(9-anthryl)benzene and Its Photoisomer: A Fundamental Moiety of Anthracene-Based π-Cluster Molecules; https://cir.nii.ac.jp/crid/1360848658060760960; Macroscopic Change in Luminescent Color by Thermally Driven Sliding Motion in [3]Rotaxanes; https://cir.nii.ac.jp/crid/1360849939495480448; 1,2,3‐Tri(9‐anthryl)benzene: Photophysical Properties and Solid‐State Intermolecular Interactions of Radially Arranged, Congested Aromatic π‐Planes**; https://cir.nii.ac.jp/crid/1360857593659825920; Long Carbon–Carbon Bonding beyond 2 Å in Tris(9-fluorenylidene)methane; https://cir.nii.ac.jp/crid/1360857593660523264; Structure and Photophysical Properties of 1,1,2,2‐Tetra(1‐anthryl)ethane: A C(sp³)−C(sp³) Bond Substituted with Four Anthracene Units; https://cir.nii.ac.jp/crid/1360857593761876864; Highly Efficient CSeCF₃ Coupling of Aryl Iodides Enabled by an Air‐Stable Dinuclear Pd^I Catalyst; https://cir.nii.ac.jp/crid/1360857595597760896; Layered compounds XXX. Unusual reaction of triple layered cyclophanes containing anthracene nucleus.; https://cir.nii.ac.jp/crid/1360857597050371584; Structural and optical investigations of charge transfer complexes involving the F4TCNQ dianion; https://cir.nii.ac.jp/crid/1360861293809418752; Room temperature charge-transfer phosphorescence from organic donor–acceptor Co-crystals; https://cir.nii.ac.jp/crid/1360861294960349952; Ultrafast charge transfer in excited electronic states and investigations into fundamental problems of exciplex chemistry: Our early studies and recent developments; https://cir.nii.ac.jp/crid/1361137044333521792; Excimer fluorescence and photodimerization of anthracenophanes and 1,2-dianthrylethanes; https://cir.nii.ac.jp/crid/1361137045954902272; A new approach to the construction of biphenylenes by the cobalt-catalyzed cocyclization of o-diethynylbenzenes with alkynes. 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The synthesis of the first cyclophane within a cyclophane - [2,2]paracyclo ([2,2]metacyclophane); https://cir.nii.ac.jp/crid/1362262944202918016; Macro Rings. I. Preparation and Spectra of the Paracyclophanes; https://cir.nii.ac.jp/crid/1362544419057886336; Layered compounds. XXIX. [2.2](2,7)Pyrenophane and its 1,13-diene; https://cir.nii.ac.jp/crid/1362825895728761984; Structure of the red, semiconducting form of 4,4',5,5'-tetramethyl-Δ^2,2'-bi-1,3-diselenole-7,7,8,8-tetracyano-<i>p</i>-quinodimethane, TMTSF–TCNQ; https://cir.nii.ac.jp/crid/1362825896025620480; Electron Delocalization in a Rigid Cofacial Naphthalene‐1,8:4,5‐bis(dicarboximide) Dimer; https://cir.nii.ac.jp/crid/1363107368688079744; Rapid Room‐Temperature, Chemoselective C−C Coupling of Poly(pseudo)halogenated Arenes Enabled by Palladium(I) Catalysis in Air; https://cir.nii.ac.jp/crid/1363107369634741248; Photodimerization of anthracenes in fluid solutions: (part 2) mechanistic aspects of the photocycloaddition and of the photochemical and thermal cleavage; https://cir.nii.ac.jp/crid/1363107370828884992; Thermally activated delayed S1 fluorescence of aromatic thiones; https://cir.nii.ac.jp/crid/1363388844953981568; Preparation and structural study of naphtho- and anthrocyclobutene derivatives which have extremely long C–C bonds; https://cir.nii.ac.jp/crid/1363670318616364160; Chemistry of multilayered cyclophanes; https://cir.nii.ac.jp/crid/1364233268395115136; [1.1]Paracyclophane. 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