A Soluble α-Dithienotetrathiafulvalene Derivative for Organic Field-effect Transistors
スポンサーリンク
概要
- 論文の詳細を見る
- 2012-04-05
著者
-
Takimiya Kazuo
Department Of Applied Chemistry Faculty Of Engineering Hiroshima University
-
Miyazaki Eigo
Department Of Applied Chemistry Graduate School Of Engineering Hiroshima University
-
Doi Iori
Department Of Applied Chemistry Graduate School Of Engineering Hiroshima University
-
Doi Iori
Department Of Applied Chemistry Faculty Of Engineering Hiroshima University
-
GOSHOME Kiyotaka
Department of Applied Chemistry, Faculty of Engineering, Hiroshima University
関連論文
- 21pGS-4 高移動度ジオクチルベンゾチエノベンゾチオフェン結晶性塗布膜のホール効果(21pGS 界面デバイス1,領域7(分子性固体・有機導体))
- 25aXP-3 チオフェンオリゴマーの超高速分光(超高速現象,領域5(光物性))
- Thermodynamic Study of an Incommensurate Organic Superconductor (MDT-TSF)(AuI_2)_(Condensed matter: structure and mechanical and thermal properties)
- 27pYL-8 有機伝導体(EDT-TSF)_2X(X=GaCl_4, FeCl_4)の結晶構造と物性(τ-型, および各種相転移,領域7(分子性固体・有機導体))
- 30pRB-2 不整合格子を有する有機超伝導体(MDT-TS)I_xBr_yの物性(30pRB 超伝導物質,領域7(分子性固体・有機導体))
- 27pYD-7 Dinaphthothienothiophene薄膜トランジスタのホール効果(界面・分子デバイス3,領域7,分子性固体・有機導体)
- 21pWB-4 有機不整合格子系伝導体(MDT-TS)(I_3)_の構造と輸送特性(陽ラジカル塩,単一成分系,領域7(分子性固体・有機導体))
- 27pYL-6 放射光を用いた有機不整合格子系超伝導体(MDT-TS)(AuI_2)_の変調構造の観測(τ-型, および各種相転移,領域7(分子性固体・有機導体))
- Isotropic Uniaxial Strain Effect on the Incommensurate Organic Superconductor: (MDT-TS)(AuI_2)_(Condensed matter: electronic structure and electrical, magnetic, and optical properties)
- 21aRA-4 不整合格子を有する有機超伝導体(MDT-TS)(AuI_2)_の巨大非線形伝導と自発交流発振(β,β''塩・高電場効果,領域7,分子性固体・有機導体)
- Development of New Semiconducting Materials for Durable High-performance Air-stable Organic Field-effect Transistors
- Molecular Modification of 2,6-Diphenylbenzo[1,2-b:4,5-b']dichalcogenophenes by Introduction of Strong Electron-withdrawing Groups : Conversion from p- to n-Channel OFET Materials
- 25pYF-10 不整合格子系有機伝導体(MDT-TS)I_Br_おける非線形伝導(25pYF 電荷秩序等,領域7(分子性固体・有機導体))
- Thin Film Characteristics and FET Performances of β-Octyl-substituted Long Oligothiophenes
- Synthesis and Photovoltaic Properties of Tetrathiafulvalene-Oligothiophene-Fullerene Triads
- Development and Photovoltaic Performance of Oligothiophene-sensitized TiO_2 Solar Cells
- 30pRB-1 有機不整合格子系伝導体(MDT-TS)(AuI_2)_の基底状態(30pRB 超伝導物質,領域7(分子性固体・有機導体))
- 新規電界発光(EL)材料として嵩高いテルフェニルピリジン,トリチルフェニルピリジンおよびテルチエニルピリジンをリガンドとするイリジウム錯体
- Anisotropic Three-dimensional Superconductivity of the Incommensurate Organic Superconductor (MDT-ST)(I_3)_(Condensed Matter : Electronic Structure, Electrical, Magnetic and Optical Properties)
- 24pYK-11 (MDT-TS)(Aul_2)_の一軸圧縮による物性(π-d系1, N-1移転,領域7(分子性固体・有機導体))
- 第50回中国四国産学連携化学フォーラム
- Dendrimer-Encapsulated Oligothiophenes
- 14aTM-2 有機不整合格子系超伝導体 (MDT-TSF)(I_3)_ のフェルミ面(陽ラジカル塩・ET 塩 : α型, 領域 7)
- Synthesis and Structures of Highly Conducting Charge-Transfer Salts of Selenium Containing TTM-TTP Derivatives
- Synthesis and Photovoltaic Effects of Oligothiophenes Incorporated with Two [60]Fullerenes
- 28pWL-12 ヨウ素無限鎖をもつ有機不整合格子系超伝導体(MDT-ST)(I_3)_の構造と電子状態(BETS塩・陽ラジカル塩)(領域7)
- 28pWL-11 不整合格子を持つ新規有機超伝導体(MDT-TS)(AuI_2)_(BETS塩・陽ラジカル塩)(領域7)
- 含セレン有機伝導体の最近の進歩 : 新合成法,新物質,新伝導体
- Synthesis and Structures of Neutral Crystals and Charge-Transfer Salts of Selenium Containing TMET-TTP Derivatives
- 20aXE-9 有機超伝導体 (MDT-TTF)_2(AuI_2) と (MDT-TSF)(AuI_2)_ の低温熱容量特性
- Oligothiophene/fullerene Dyads as Active Photovoltaic Materials
- 28aZA-6 ヨウ素無限鎖をもつ超伝導性有機不整合結晶 (MDT-ST) (I_3)_ の超伝導特性
- 次世代エレクトロニクス素子に向けた ナノ共役分子の開発と機能
- Preparation and Characterization of Novel Aromatic-inserted Tris-fused Tetrathiafulvalenes
- Synthesis, Structures, and Properties of Two Isomeric Naphthodithiophenes and Their Methyl, Methylthio, and 2-Thienyl Derivatives ; Application to Coductive Charge-Transfer Complexes and Low-Bandgap Polymers
- Synthess, Optical, and Conductive Properties of Long Oligothiophenes and Their Utilization as Molecular Wires
- Synthesis and Properties of a Series of the Longest Oligothiophenes up to the 48-mer
- Structures and Properties of (TMEO-ST-TTP)_2AsF_6
- Syntheses and Properties of 11,11,12,12-Tetracyano-2,6-anthraquinodimethane (TANT) and Its 9,10-Dichloro Derivative as Novel Extensive Electron Acceptors
- Double - Bridged Tetrathiafulvalenophanes as Novel Electron Donors : Syntheses, Structures, and Properties of Three Structural Isomers
- Facile Preparation and Charge-Transfer Complexes of Naphtho[1,8-bc:4,5-b'c']dithiophene and 2,5-Dimethyl and Bis(methylthio) Derivatives
- Facile Preparation and Charge-Transfer Complexes of Naphtho[1,8-bc:4,5-b'c']dithiophene and 2,5-Dimethyl and Bis(methylthio) Derivatives
- Alkylated 2,6-Bis(dicyanomethylene)-2,6-dihydrobenzo[1,2-b:4,5-b']dithiophenes : New Soluble n-Channel Organic Semiconductors for Air-stable OFETs
- Molecular Modification of 2,7-Diphenyl[1]benzothieno[3,2-b]benzothiophene (DPh-BTBT) with Diarylamino Substituents : From Crystalline Order to Amorphous State in Evaporated Thin Films
- Unique Molecular Arrangement in Semiconducting Layer and FET Characteristics of Thin Film Transistors Based on 2,6-Dialkylbenzo[1,2-b:4,5-b']diselenophenes (C_n-BDSs)
- 2,6-Dialkylbenzo[1,2-b:4,5-b']dithiophenes (C_n-BDTs) as Soluble Organic Semiconductors for Solution-processed Organic Field-effect Transistors
- 23pRL-7 高移動度低分子材料C_8-BTBTにおけるキャリアの電場誘起ESR観測(23pRL 界面デバイス1,領域7(分子性固体・有機導体))
- 24pRL-10 塗布結晶化法による有機半導体単結晶とその高移動度トランジスタ特性(24pRL 界面デバイス2,領域7(分子性固体・有機導体))
- Aminopropyl-Glucose Sequentially Grafted Mesoporous Silica Nanocomposite as a Novel Boron Adsorbent
- Conductive, Magnetic, and Optical Properties of Sterically Hindered Dodecithiophenes. Evidence for the Coexistence of Bipolaron and π-Dimer
- Synthesis and Characterization of N-Acyl-substituted PyrroloTTF Derivatives and Improved Air-stability of PyrroloTTF-based OFETs
- Structures and Electrical Properties of β- and θ-(BTM-TTP)_2SbF_6
- New Stable Metallic Salt Based on a Donor Molecule Containing peri-Ditellurium Bridges, TMTTeN(SCN)_
- Spectroscopic Study of Isostructural Charge-Transfer Salts:Non-metallic DMTTA-BF_4 and Metallic DMTSA-BF_4
- Metallic Properties of 1:1 Charge-Transfer Salt,Dimethyltetraselenoanthracene-Tetrafluoroborate (DMTSA-BF_4)
- TTF-Cytosine Dyad as an Electron-donor Molecule Having Proton-accepting Ability : Formation of Hemiprotonated Cytosine Dimer in I_3^- Salt
- Introduction of Amino Groups into the Dibenzo-TTF π-System : Enhanced Electron-Donating Ability and Intermolecular Hydrogen Bonding
- Transformation of Double Hydrogen-bonding Motifs of TTF-Uracil System by Redox Change
- First Syntheses of Iodinated1,6-Dithiapyrene Derivatives
- 23pRL-2 高移動度有機半導休材料の孤立分子のESR解析(23pRL 界面デバイス1,領域7(分子性固体・有機導体))
- Recent Synthetic Advances of Tetrathiafulvalene-Based Organic Conductors
- Synthesis and Properties of Bis(ethyleneseleno)tetrathiafulvalene (BES-TTF) and Diselenolotetrathiafulvalene (DS-TTF) as Novel Electron Donors
- Synthesis and Properties of New Tetrathiapentalene Donors Composed of Vinylogous TTFs
- Structures and Electrical Properties of (BTM-TS-TTP)_4PF_6
- WANTS-NEEDS-SEEDS 3次元有機トランジスタ--縦型チャネルの集積化による有機トランジスタの高性能化
- Solution-Processed Dioctylbenzothienobenzothiophene-Based Top-Gate Organic Transistors with High Mobility, Low Threshold Voltage, and High Electrical Stability
- Very High Mobility in Solution-Processed Organic Thin-Film Transistors of Highly Ordered [1]Benzothieno[3,2-b]benzothiophene Derivatives
- Three Structural Isomers of Dinaphthothieno[3,2-b]thiophenes : Elucidation of Physicochemical Properties, Crystal Structures, and Field-Effect Transistor Characteristics
- Efficient Photocurrent Generation at Dinaphtho[2,3-b:2',3'-f]thieno[3,2-b]thiophene/C_ Bilayer Interface
- 28aTN-7 C_8-BTBTのFETデバイスにおける電場誘起ESR信号のシミュレーション解析(28aTN 界面デバイス,領域7(分子性固体・有機導体))
- Two Isomeric Didecyl-dinaphtho〔2,3-b:2',3'-f〕thieno〔3,2-b〕thiophenes : Impact of Alkylation Positions on Packing Structures and Organic Field Effect Transistor Characteristics (Special Issue : Applied Physics on Materials Research)
- A Soluble α-Dithienotetrathiafulvalene Derivative for Organic Field-effect Transistors
- Electroconductive π-Junction Au Nanoparticles
- Development of Organic Conductors with Self-Assembled Architectures of Biomolecules : Synthesis and Crystal Structures of Nucleobase-Functionalized Tetrathiafulvalene Derivatives
- Syntheses and Properties of Dimethyl and Tetramethyl Anthra(1,9-cd:4,10-c'd')bis(1,2)dichalcogenoles and Their Charge-Transfer Complexes.