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Unencapsulated Air-stable Organic Field Effect Transistor by All Solution Processes for Low Power Vapor Sensing.High mobility polymer based on a π-extended benzodithiophene and its application for fast switching transistor and high gain photoconductor.Outlook and emerging semiconducting materials for ambipolar transistors.Qualitatively Incorrect Features in the TDDFT Spectrum of Thiophene-Based Compounds.Reducing dynamic disorder in small-molecule organic semiconductors by suppressing large-amplitude thermal motions.Heteroaromatic organic compound with conjugated multi-carbonyl as cathode material for rechargeable lithium batteriesRemarkable enhancement of charge carrier mobility of conjugated polymer field-effect transistors upon incorporating an ionic additive.Synthesis and Properties of Fully-Conjugated Indacenedithiophenes.Heteroatom substituted organic/polymeric semiconductors and their applications in field-effect transistors.Recent developments in synthetic methods for benzo[b]heteroles.Naphthobischalcogenadiazole Conjugated Polymers: Emerging Materials for Organic Electronics.Charge carrier mobility in organic molecular materials probed by electromagnetic waves.High-performance vertical organic transistors.Liquid crystals for organic thin-film transistors.Synthesis and characterization of heterofluorenes containing four-coordinated group 13 elements: theoretical and experimental analyses and comparison of structures, optical properties and electronic states.Thermal Molding of Organic Thin-Film Transistor Arrays on Curved Surfaces.Palladium(ii)-catalyzed synthesis of dibenzothiophene derivatives via the cleavage of carbon-sulfur and carbon-hydrogen bondsVersatile telluracycle synthesis via the sequential electrophilic telluration of C(sp2)-Zn and C(sp2)-H bonds.Syntheses of dibenzo[d,d']benzo[2,1-b:3,4-b']difuran derivatives and their application to organic field-effect transistors.Regioselective synthesis of C3 alkylated and arylated benzothiophenes.Enhanced performance of benzothieno[3,2-b]thiophene (BTT)-based bottom-contact thin-film transistors.Furan fused V-shaped organic semiconducting materials with high emission and high mobility.Extended conjugated donor-acceptor molecules with E-(1,2-difluorovinyl) and diketopyrrolopyrrole (DPP) moieties toward high-performance ambipolar organic semiconductors.Solution-processed anthradithiophene-PCBM p-n junction photovoltaic cells fabricated by using the photoprecursor method.A dicyanomethylene-substituted triangulene: effects of molecular-symmetry reduction and electron-accepting substituents on a fused polycyclic neutral π-radical system.Close encounters of the 3D kind - exploiting high dimensionality in molecular semiconductors.V-shaped organic semiconductors with solution processability, high mobility, and high thermal durability.Effects of stereoisomerism on the crystallization behavior and optoelectrical properties of conjugated molecules.Facile access to unsymmetrically substituted tellurium-boron based heterocycles.High activity and stability in the cross-coupling of aryl halides with disulfides over Cu-doped hierarchically porous zeolite ZSM-5.A series of π-extended thiadiazoles fused with electron-donating heteroaromatic moieties: synthesis, properties, and polymorphic crystals.Robust ethylenedioxythiophene-vinylene oligomers from fragile thiophene-vinylene cores: synthesis and optical, chemical and electrochemical properties of multicharged shapes.Multistep π dimerization of tetrakis(n-decyl)heptathienoacene radical cations: a combined experimental and theoretical study.Highly bent crystals formed by restrained π-stacked columns connected via alkylene linkers with variable conformations.Photooxidation of a Twisted Isoquinolinone.Synthesis and Properties of New N-Heteroheptacenes for Solution-Based Organic Field Effect Transistors.Ladder-type Heteroarenes: Up to 15 Rings with Five Imide Groups.Reversibility of temperature driven discrete layer-by-layer formation of dioctyl-benzothieno-benzothiophene films.Effects of chalcogen atom substitution on the optoelectronic and charge-transport properties in picene-type π-systems.Acid-induced chemoselective arylthiolations of electron-rich arenes in ionic liquids from sodium arylsulfinates: the reducibility of halide anions in [Hmim]Br.
P2860
Q27350149-9DAA40A1-5AC2-43DD-B029-C6051DBE5103Q33813826-5E0A3288-57E3-4533-9211-181DBC506F89Q35109845-E45D7495-969A-4CE0-8416-ED65B818D24AQ36136537-5DCDEC50-3D9A-4AA3-8482-A4D98E0F144BQ36610976-B884F70D-D4B2-41A7-A74B-E2BD808CB7F7Q36786458-2F4C2BCC-7262-41C3-8C04-F4911765B516Q37056183-A1923B10-7B29-453F-90C2-6D2F07F9666AQ37692005-45BA17DB-FED3-4A10-A897-E799F86ED6CEQ38192547-DDEA0224-F3AB-47C4-A726-A435ABC9249EQ38739731-735B6997-6589-46EF-8C18-9ADD09E0120FQ39152638-822080CC-B6D0-4E98-A490-9F6125CDC9E6Q39202047-167968E8-7CEC-425D-835E-B7B875286DB1Q39426466-01445E65-4013-4DDC-891E-D80A20D0D861Q39793082-AE0854B5-DEB5-441B-979E-C6AB3A09123FQ41100434-8F128038-6324-425B-B9DD-4DACBA31AF23Q41895818-8ADEC863-748C-454D-93FD-BA2290D67091Q41941753-9D4E26B4-CCAD-463E-BE01-83B9835B79B8Q42037977-1B2AA8AE-E34D-4291-9258-62E032D642A6Q42154148-4AC630CF-ADAE-4B4F-9864-8BE6653E22FEQ42314476-1F222306-7C7D-48AE-9728-8D1A044801B8Q43477595-0D74A4F5-F1BF-47D7-838D-EE4121D7B135Q43505105-F4504606-5D0F-40C9-8BD1-5910EB64C822Q43594997-2920E66F-83A9-4295-AF71-E7CDB82C3F6BQ44133175-1EACE146-4AAA-4045-93F9-5B53645184C2Q44964247-E7EF1D98-C445-4ECE-9DD2-590C3F4903F3Q45339305-F35EAC00-4D83-4F15-B892-43617AF055D6Q46009112-93B599D8-BB12-45C6-ACC2-7F65CA270F97Q46178174-A6ADA30E-87E1-493F-9EF6-40470F6FFCDDQ46360314-F55B5938-4751-4708-854C-C3D77A51E000Q46765796-2462BD84-B666-4E58-B9B1-D1FB952A9CE1Q46795521-AFC9AA9C-3C23-4F6E-8A42-8E170AED8179Q46812380-5F4D25F5-ABF4-45C4-9182-8786C4A2637BQ46864068-117F8EEE-B315-4CB3-B58D-46EDFB8D11EEQ47111549-271434E9-D05E-46DF-8D20-EE9593AF1F1FQ47571661-07CCC222-C3F9-4477-A548-C41A6EE69954Q47910795-1717CB8E-2332-4781-90B7-031C56BEBBF4Q47979110-3339233A-DEE3-4289-94B9-FA0DC3AFF436Q48045852-3C9B1634-DB25-4496-89D9-66D008FB92E4Q48104772-4358F14B-F45E-4C76-A6A3-BC3AF415AA4CQ48147481-AB04D877-C55B-4255-87B5-C4ECD0D11483
P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Thienoacene-based organic semiconductors.
@en
Thienoacene-based organic semiconductors.
@nl
type
label
Thienoacene-based organic semiconductors.
@en
Thienoacene-based organic semiconductors.
@nl
prefLabel
Thienoacene-based organic semiconductors.
@en
Thienoacene-based organic semiconductors.
@nl
P2860
P356
P1433
P1476
Thienoacene-based organic semiconductors
@en
P2093
Eigo Miyazaki
Shoji Shinamura
P2860
P304
P356
10.1002/ADMA.201102007
P407
P577
2011-08-15T00:00:00Z