Naked-eye-detectable supramolecular sensing system for glutaric acid and isophthalic acid

• 資料種別: 記事
• タイトル: Naked-eye-detectable supramolecular sensing system for glutaric acid and isophthalic acid
• 著者・編者: Atsuya Muranaka; Hayato Ban; Masaya Naito
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2022-08-11
• 出版年（W3CDTF）: 2022-08-11
• タイトル（掲載誌）: Bulletin of the Chemical Society of Japan
• 巻号年月日等（掲載誌）: 95(10)
• 掲載巻: 95(10)
• 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.20220195; https://doi.org/10.1246/bcsj.20220195
• 国立国会図書館永続的識別子: info:ndljp/pid/12686455; https://dl.ndl.go.jp/pid/12686455
• 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）: 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/95/10
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/12686454; https://dl.ndl.go.jp/pid/12686454
• 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.20220195; https://doi.org/10.1246/bcsj.20220195
• 関連情報: CCDC 2158287: Experimental Crystal Structure Determination; https://cir.nii.ac.jp/crid/1883116918088001664
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/12686455; https://dl.ndl.go.jp/pid/12686455; https://academic.oup.com/bcsj/article-pdf/95/10/1428/56314592/bcsj.20220195.pdf
• 参照: Lateral nanoarchitectonics from nano to life: ongoing challenges in interfacial chemical science; https://cir.nii.ac.jp/crid/1050302315064477824; Bio-gel nanoarchitectonics in tissue engineering; https://cir.nii.ac.jp/crid/1050582385449346560; Composite Nanoarchitectonics Towards Method for Everything in Materials Science; https://cir.nii.ac.jp/crid/1050301684637078144; Nanoarchitectonics: the method for everything in materials science; https://cir.nii.ac.jp/crid/1360865819405448192; Identification of Water-Soluble Polymers through Machine Learning of Fluorescence Signals from Multiple Peptide Sensors; https://cir.nii.ac.jp/crid/1360865814751943552; Interfacial nanoarchitectonics with porphyrins and related molecules: Langmuir-Blodgett method and layer-by-layer assembly; https://cir.nii.ac.jp/crid/1360021391865044224
• 参照: Four- and two-armed hetero porphyrin dimers: their specific recognition and self-sorting behaviours; https://cir.nii.ac.jp/crid/1360576118829498880; Carboxylic acid recognition of a tetraamidine having a tetraphenylethylene unit based on aggregation-induced emission; https://cir.nii.ac.jp/crid/1360857593805850880; Straight from the bottle! Wine and juice dicarboxylic acids as templates for supramolecular cage self-assembly; https://cir.nii.ac.jp/crid/1360579820045920384; Magnetic Circular Dichroism of <i>meso</i>-Phenyl-Substituted Pd-Octaethylporphyrins; https://cir.nii.ac.jp/crid/1360579819749054208; A Five‐layer π‐Aromatic Structure Formed through Self‐assembly of a Porphyrin Trimer and Two Aromatic Guests; https://cir.nii.ac.jp/crid/1360290617721143424; Molecular recognition and sensing of dicarboxylates and dicarboxylic acids; https://cir.nii.ac.jp/crid/1360011144413560192; Molecular Cursor Caliper: A Fluorescent Sensor for Dicarboxylate Dianions; https://cir.nii.ac.jp/crid/1361981469623402880; Designed Conformation and Fluorescence Properties of Self-Assembled Phenazine-Cored Platinum(II) Metallacycles; https://cir.nii.ac.jp/crid/1360855568574573696; A Turn-on Fluorescence Sensor for Dicarboxylic Acids Based on Aggregation-induced Emission; https://cir.nii.ac.jp/crid/1360290709485560064; Discrimination of dicarboxylic acids <i>via</i> assembly-induced emission; https://cir.nii.ac.jp/crid/1362262946359026816; Cofacial porphyrin dimers assembled from N-heterocyclic carbene–metal bonds; https://cir.nii.ac.jp/crid/1360016870600489344; Molecular recognition by multiple metal coordination inside wavy-stacked macrocycles; https://cir.nii.ac.jp/crid/1050001202649183104; Triphenylamine‐Based Open and Macrocyclic Receptors: A Study Towards Selectivite Recognition of Aliphatic Dicarboxylates; https://cir.nii.ac.jp/crid/1360016865847821952; Triggering Assembly and Disassembly of a Supramolecular Cage; https://cir.nii.ac.jp/crid/1361981470225272960; Magnetic Circular Dichroism Spectroscopy of <i>meso</i>-Tetraphenylporphyrin-Derived Hydroporphyrins and Pyrrole-Modified Porphyrins; https://cir.nii.ac.jp/crid/1360574096202681856; Preorganized Fluorescent Receptor for the Preferential Binding of the Glutarate Anion; https://cir.nii.ac.jp/crid/1361137045991831040; Complexation and sensing of dicarboxylate anions and dicarboxylic acids; https://cir.nii.ac.jp/crid/1361418520349301760; Translation of Dicarboxylate Structural Information to Fluorometric Optical Signals through Self‐Assembly of Guanidinium‐Tethered Oligophenylenevinylene; https://cir.nii.ac.jp/crid/1360285704968092928; New carbazolo[1,2-a]carbazole derivative as ionophore for anion-selective electrodes: Remarkable recognition towards dicarboxylate anions; https://cir.nii.ac.jp/crid/1360861292546931968; Porphyrin-based sensor nanoarchitectonics in diverse physical detection modes; https://cir.nii.ac.jp/crid/1360565166834164608; A viologen-urea-based anion receptor: Colorimetric sensing of dicarboxylate anions; https://cir.nii.ac.jp/crid/1360016869158230912; Four-component assembly in the crystalline state driven by amidinium–carboxylate salt bridge formation from an aqueous solution; https://cir.nii.ac.jp/crid/1363951794328882944; Unusual conformational preference of an aromatic secondary urea: solvent-dependent open-closed conformational switching of N,N′-bis(porphyrinyl)urea; https://cir.nii.ac.jp/crid/1360004233565921408; Diagnosis and management of glutaric aciduria type I – revised recommendations; https://cir.nii.ac.jp/crid/1360861290854222208; Synthesis, Binding and Fluorescence Studies of Bis-2-amidopyrrole Receptors for Bis-carboxylate Anions; https://cir.nii.ac.jp/crid/1360861293017268480; Effects of Basis Set Superposition Error on Optimized Geometries and Complexation Energies of Organo-Alkali Metal Cation Complexes; https://cir.nii.ac.jp/crid/1360016868099698688; Application of MCD spectroscopy to porphyrinoids; https://cir.nii.ac.jp/crid/1363951793438204288; Highly Enantioselective Recognition of Dicarboxylic Acid Substrates by the Control of Nonlinear Responses; https://cir.nii.ac.jp/crid/1360011144052000000; Triphenylamine-based novel PET sensors in selective recognition of dicarboxylic acids; https://cir.nii.ac.jp/crid/1360574094858956928; Anthracene-coupled Pyridine Amines: A New “Off–On” Switch for Molecular Recognition Studies on Dicarboxylic Acids; https://cir.nii.ac.jp/crid/1360283694087534464; Directed H-bonding inhibition in molecular recognition: an NMR case study of the H-bonding of a dicarboxylic acid with a new mixed diamide receptor having one adjacent pyridine-N-oxide; https://cir.nii.ac.jp/crid/1360579818180644864; Binuclear Cu2+ complex mediated discrimination between l-glutamate and l-aspartate in water; https://cir.nii.ac.jp/crid/1360016867247322752; A Dimetallic Cage with a Long Ellipsoidal Cavity for the Fluorescent Detection of Dicarboxylate Anions in Water; https://cir.nii.ac.jp/crid/1363670319337690368; Synthetic receptors for carboxylic acids and carboxylates; https://cir.nii.ac.jp/crid/1360011144123042816; Sensitivity and specificity of free and total glutaric acid and 3‐hydroxyglutaric acid measurements by stable‐isotope dilution assays for the diagnosis of glutaric aciduria type I; https://cir.nii.ac.jp/crid/1361981468561563392; Syn-Anti Conformational Changes in Zinc Porphyrin Dimers Induced by Temperature-Controlled Alcohol Ligation; https://cir.nii.ac.jp/crid/1361137044281496704; Efficient chirality transcription utilizing a cerium(IV) double decker porphyrin: a prototype for development of a molecular memory system; https://cir.nii.ac.jp/crid/1360292621559357952; Cystinophanes, a Novel Family of Aromatic-Bridged Cystine Cyclic Peptides: Synthesis, Crystal Structure, Molecular Recognition, and Conformational Studies; https://cir.nii.ac.jp/crid/1360855571398971264; Molecular Recognition: The Demonstration of 1,3-Bis[(pyrid-2-ylamino)carbonyl]adamantane as an Exceptionally Versatile Assembler of One-Dimensional Motifs; https://cir.nii.ac.jp/crid/1362544419517500288; Novel electrochemical sensors for neutral molecules; https://cir.nii.ac.jp/crid/1364233269292614784; Self-Assembling, Chromogenic Receptors for the Recognition of Dicarboxylic Acids; https://cir.nii.ac.jp/crid/1363388845318094464; Metal templated receptors for the effective complexation of dicarboxylates; https://cir.nii.ac.jp/crid/1362825893427847680; Hydrogen-bonding control of molecular self-assembly: formation of a 2 + 2 complex in solution and in the solid state; https://cir.nii.ac.jp/crid/1360011145621043584; Molecular recognition: hydrogen-bonding receptors that function in highly competitive solvents; https://cir.nii.ac.jp/crid/1361981468347216896; Molecular recognition: a remarkably simple receptor for the selective complexation of dicarboxylic acids; https://cir.nii.ac.jp/crid/1360011145179286016; Dabco-metalloporphyrin binding: ternary complexes, host-guest chemistry and the measurement of .pi.-.pi. interactions; https://cir.nii.ac.jp/crid/1360855571111852544; Synthesis of naphthalene-bridged porphyrin dimers and their orientation-dependent exciton coupling; https://cir.nii.ac.jp/crid/1361137044630397312; Anion receptor molecules. Chain length dependent selective binding of organic and biological dicarboxylate anions by ditopic polyammonium macrocycles; https://cir.nii.ac.jp/crid/1363388843383932160; LCAO MO SCFπ-electron calculations on the magnetic circular dichroism of porphin, protoporphyrin, and porphyrin a; https://cir.nii.ac.jp/crid/1360574094578347520
• 参照（URI）: https://cir.nii.ac.jp/crid/1370298339664521366; https://cir.nii.ac.jp/crid/1370298339664521353; https://cir.nii.ac.jp/crid/1370298339664521363
• 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: 国立国会図書館デジタルコレクション; https://dl.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