2,6-Diphenylbenzo[1,2-<i>b</i>:4,5-<i>b</i>‘]dichalcogenophenes: A New Class of High-Performance Semiconductors for Organic Field-Effect Transistors
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CiNii Research
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- 資料種別
- 記事
- 出版年月日等
- 2004-04-03
- 出版年（W3CDTF）
- 2004-04-03
- タイトル（掲載誌）
- Journal of the American Chemical Society
- 巻号年月日等（掲載誌）
- 126 16
- 掲載巻
- 126
- 掲載号
- 16
- 掲載ページ
- 5084-5085
- 掲載年月日（W3CDTF）
- 2004-04-03
- ISSN（掲載誌）
- 00027863
- 出版事項（掲載誌）
- American Chemical Society (ACS)
- 対象利用者
- 一般
- 標準番号（その他）
- PMID : 15099088
- DOI
- 10.1021/ja0496930
- 作成日（W3CDTF）
- 2004-04-21
- 関連情報
- CCDC 239697: Experimental Crystal Structure Determination
- 参照
- Construction of Thienothiophene and Thienofuran Ring Systems via Ring Expansion of Difluorothiiranes Generated from DithioestersConstruction of Pinpoint-Fluorinated Benzothiophene Frameworks Using Palladium-Catalyzed Cyclization of o-(Fluorovinyl)phenyl-Substituted ThiophenesDirect Synthesis of Benzoselenophene and Benzothiophene Derivatives from 1,1-Diarylethenes and Biaryls by Chalcogen Cation-Mediated Successive Bond FormationNaphtho[2,3-<i>b</i>:6,7-<i>b</i>′]dichalcogenophenes: Syntheses, Characterizations, and Chalcogene Atom Effects on Organic Field-Effect Transistor and Organic Photovoltaic DevicesEffects of Selenium Atoms on [1]Benzochalcogenopheno[3,2-<i>b</i>][1]benzochalcogenophene-based Organic SemiconductorsAlkylated 2,6-Bis(dicyanomethylene)-2,6-dihydrobenzo[1,2-<i>b</i>:4,5-<i>b</i>′]dithiophenes: New Soluble n-Channel Organic Semiconductors for Air-stable OFETsAir-Stable and High-Mobility Organic Semiconductors Based on Heteroarenes for Field-Effect TransistorsSolution-Processed and Air-Stable n-Type Organic Thin-Film Transistors Based on Thiophene-Fused Dicyanoquinonediimine (DCNQI) DeriativesAngular-shaped naphthodifurans, naphtho[1,2-b;5,6-b′]- and naphtho[2,1-b;6,5-b′]-difuran: are they isoelectronic with chrysene?Naphthodithiophenes as building units for small molecules to polymers; a case study for in-depth understanding of structure–property relationships in organic semiconductorsSynthesis and characterization of heterofluorenes containing four-coordinated group 13 elements: theoretical and experimental analyses and comparison of structures, optical properties and electronic statesSelf-organized one-dimensional columns of benzo[b]thiophene-fused tetraazaporphyrinsSodium Sulfide-Promoted Thiophene-Annulations: Powerful Tools for Elaborating Organic Semiconducting MaterialsLinear- and Angular-Shaped Naphthodithiophenes: Selective Synthesis, Properties, and Application to Organic Field-Effect TransistorsBis(methylthio)tetracenes: Synthesis, Crystal-Packing Structures, and OFET PropertiesDithiophene-Fused Tetracyanonaphthoquinodimethanes (DT-TNAPs): Synthesis and Characterization of π-Extended Quinoidal Compounds for n-Channel Organic SemiconductorNovel Field-effect Transistors Based on Bis(1,3-dithiol-2-ylidene) Compounds with a Conjugated Spacer GroupSynthesis and structure of bis(ethylenedioxy)‐1,4,5,8‐tetraselenanaphthaleneOrthogonally Functionalized Naphthodithiophenes: Selective Protection and BorylationLargely π-Extended Thienoacenes with Internal Thieno[3,2-<i>b</i>]thiophene Substructures: Synthesis, Characterization, and Organic Field-Effect Transistor ApplicationsEffects of chalcogen atom substitution on the optoelectronic and charge-transport properties in picene-type π-systemsNaphthobischalcogenadiazole Conjugated Polymers: Emerging Materials for Organic ElectronicsIsomerically Pure Anthra[2,3-<i>b</i>:6,7-<i>b</i>′]-difuran (<i>anti</i>-ADF), -dithiophene (<i>anti</i>-ADT), and -diselenophene (<i>anti</i>-ADS): Selective Synthesis, Electronic Structures, and Application to Organic Field-Effect TransistorsSynthesis, Properties, Crystal Structures, and Semiconductor Characteristics of Naphtho[1,2-<i>b</i>:5,6-<i>b</i>′]dithiophene and -diselenophene DerivativesBilayered Crystalline Organic Semiconductors for Solution-processed OFETs: Asymmetrically-substituted Smectic Liquid Crystal of Benzo[1,2-b:4,5-b′]dithiophene DerivativesBis(ethylenedioxy)-1,4,5,8-tetraselenanaphthalene: The First Example of Tetraselenanaphthalene2,6-Dialkylbenzo[1,2-<i>b</i>:4,5-<i>b</i>′]dithiophenes (C<i>n</i>-BDTs) as Soluble Organic Semiconductors for Solution-processed Organic Field-effect Transistors[1]Benzothieno[3,2-b][1]benzothiophenes- and dinaphtho[2,3-b:2′,3′-f]thieno[3,2-b]thiophene-based organic semiconductors for stable, high-performance organic thin-film transistor materialsU‐Shaped Heteroacenes Embedded with Heavy Chalcogen Atoms: Unique Bilayer Self‐Organization of Crooked π‐Cores Enabling Efficient Charge TransportThienoacene‐Based Organic SemiconductorsThienannulation: Efficient Synthesis of π‐Extended Thienoacenes Applicable to Organic SemiconductorsMolecular Modification of 2,6-Diphenylbenzo[1,2-<i>b</i>:4,5-<i>b</i>′]dichalcogenophenes by Introduction of Strong Electron-withdrawing Groups: Conversion from p- to n-Channel OFET MaterialsUnique Molecular Arrangement in Semiconducting Layer and FET Characteristics of Thin Film Transistors Based on 2,6-Dialkylbenzo[1,2-<i>b</i>:4,5-<i>b</i>′]diselenophenes (C<i>n</i>-BDSs)Effect of thiophene/furan substitution on organic field effect transistor properties of arylthiadiazole based organic semiconductorsQuinoidal Acenedichalcogenophenediones for Near-Infrared-Absorbing Organic Semiconductors: Effects of Chalcogen Atom Substitution on the Physicochemical and Carrier Transport PropertiesSemiconductor Properties of π‐Extended 2‐(Thiopyran‐4‐ylidene)‐1,3‐benzodithiole (TP‐BT) AnalogsSynthesis and chiroptical properties of stereogenic cyclic dimers based on 2,2′-biselenophene and [2.2]paracyclophaneDevelopment of New Semiconducting Materials for Durable High‐Performance Air‐Stable Organic Field‐Effect Transistors.Single-Crystal Field-Effect Transistors Based on Organic Selenium-Containing SemiconductorVol. 90 Commemorative Account : Fascinating Molecules and Reactions : The Chemical Society of Japan Award for Creative Work for 2014 : Thiophene-Fused Naphthalene Diimides : New Building Blocks for Electron Deficient π-Functional Materials
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- 国立情報学研究所 : CiNii Research
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