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Highly Efficient and Stable Solar Cells Based on Thiazolothiazole and Naphthobisthiadiazole Copolymers.High-efficiency polymer solar cells with small photon energy loss.Thienoacene-based organic semiconductors.Towards colorless transparent organic transistors: potential of benzothieno[3,2-b]benzothiophene-based wide-gap semiconductors.Quinacridone-Diketopyrrolopyrrole-Based Polymers for Organic Field-Effect Transistors.Tuning the effective spin-orbit coupling in molecular semiconductors.Organic superconductors with an incommensurate anion structure.Naphthobischalcogenadiazole Conjugated Polymers: Emerging Materials for Organic Electronics.5, 10-linked naphthodithiophenes as the building block for semiconducting polymers.Dinaphthopentalenes: pentalene derivatives for organic thin-film transistors.High-mobility semiconducting naphthodithiophene copolymers.Synthesis, properties, crystal structures, and semiconductor characteristics of naphtho[1,2-b:5,6-b']dithiophene and -diselenophene derivatives.Quinoidal oligothiophenes: towards biradical ground-state species.Flexible low-voltage organic transistors with high thermal stability at 250 °C.Synthetic procedure for various selenium-containing electron donors of the bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) type.Thiophene-thiazolothiazole copolymers: significant impact of side chain composition on backbone orientation and solar cell performances.2,6-Diphenylbenzo[1,2-b:4,5-b']dichalcogenophenes: a new class of high-performance semiconductors for organic field-effect transistors.2,6-Diarylnaphtho[1,8-bc:5,4-b'c']dithiophenes as new high-performance semiconductors for organic field-effect transistors.Very Strong Binding for a Neutral Calix[4]pyrrole Receptor Displaying Positive Allosteric Binding.Reversible Dimerization and Polymerization of a Janus Diradical To Produce Labile C-C Bonds and Large Chromic Effects.Syntheses, structures, spectroscopic properties, and pi-dimeric interactions of [n.n]quinquethiophenophanes.Polyether-bridged sexithiophene as a complexation-gated molecular wire for intramolecular photoinduced electron transfer.Fluorescence up-conversion study of excitation energy transport dynamics in oligothiophene-fullerene linked dyads.Highly soluble [1]benzothieno[3,2-b]benzothiophene (BTBT) derivatives for high-performance, solution-processed organic field-effect transistors.Changes in electrochemical and optical properties of oligoalkylthiophene film induced by bipolaron formation.Synthesis and photophysical properties of two dual oligothiophene-fullerene linkage molecules as photoinduced long-distance charge separation systems.Effects of extension or prevention of pi-conjugation on photoinduced electron transfer processes of ferrocene-oligothiophene-fullerene triads.Drastic change of molecular orientation in a thiazolothiazole copolymer by molecular-weight control and blending with PC61BM leads to high efficiencies in solar cells.Methylthionated benzo[1,2-b:4,5-b']dithiophenes: a model study to control packing structures and molecular orientation in thienoacene-based organic semiconductors.N,N'-Bis(2-cyclohexylethyl)naphtho[2,3-b:6,7-b']dithiophene Diimides: Effects of Substituents.[2,2']Bi[naphtho[2,3-b]furanyl]: a versatile organic semiconductor with a furan-furan junction.Linear- and angular-shaped naphthodithiophenes: selective synthesis, properties, and application to organic field-effect transistors.Soluble Dinaphtho[2,3-b:2',3'-f]thieno[3,2-b]thiophene Derivatives for Solution-Processed Organic Field-Effect Transistors.Solution-processible n-channel organic field-effect transistors based on dicyanomethylene-substituted terthienoquinoid derivative.Dithienyl Acenedithiophenediones as New π-Extended Quinoidal Cores: Synthesis and Properties.Facile synthesis of highly pi-extended heteroarenes, dinaphtho[2,3-b:2',3'-f]chalcogenopheno[3,2-b]chalcogenophenes, and their application to field-effect transistors.2,7-Diphenyl[1]benzothieno[3,2-b]benzothiophene, a new organic semiconductor for air-stable organic field-effect transistors with mobilities up to 2.0 cm2 V(-1) s(-1).Hybrid organic semiconductors including chalcogen atoms in pi-conjugated skeletons. Tuning of optical, redox, and vibrational properties by heavy atom conjugation.Implication of Fluorine Atom on Electronic Properties, Ordering Structures, and Photovoltaic Performance in Naphthobisthiadiazole-Based Semiconducting Polymers.N,N'-Unsubstituted Naphthodithiophene Diimide: Synthesis and Derivatization via N-Alkylation and -Arylation.
P50
Q36099526-E2B4941C-F62D-41FB-AAA7-5A80DF99B1B1Q36392333-4322E938-A5A3-4E33-9C4F-F039743FD69FQ37917706-F6EBB50F-3F9C-4DFF-859D-C9351FAE20AFQ38441667-1C4F7C43-BC21-40AB-9832-F549F0174286Q38624093-306ACC15-B8CD-4CF8-AFC3-797EE4F51293Q38685366-1BD95D4F-EBED-4D93-86CC-9830479B7B31Q39017265-5FAD508B-FE23-4F53-B4CB-1C26CAAE85DAQ39152638-DEEA1911-F277-4D0B-BA61-A749A90227F1Q41645284-59E17F91-BB7A-4FC4-B961-6565BE05011AQ42909428-E991B462-C195-4286-B0C1-B4639BB9CF7EQ43125248-23CA05D6-3E32-4FB2-81FF-4E8C21ED3454Q43184693-6DEBBE3E-F85A-4828-B129-8C96FE39742EQ43235850-ECB55633-10D5-4C9B-895F-ECB7FE1DDF78Q43471945-0C175D62-59BB-4654-8E4F-74AE9B60C891Q44021241-2DC8D86B-25A9-47A1-85A5-A5248B1F68CBQ44713395-CA544A08-A555-42D7-BF82-A3C6A4B23D06Q44852388-7FE09DB8-7F45-4F45-97C5-80C874391347Q45310161-C476BDA8-AF5B-4271-A35B-C6C3A77B843BQ46427846-88B18E21-6948-417A-BDC5-DC8FAA391E81Q46470963-CF9ADF5D-7D41-4ED0-8C0C-48CB1FB10454Q46519606-7C1BBE25-F3CA-4E50-87AC-805807104853Q46785312-E36F0B00-00CB-4426-9E8A-7FE0526DFD37Q46797510-08C06F4B-2BBD-4EE2-9022-47367CFB9E1CQ46877463-3134ED2B-1BFA-42F1-8B92-587DA6F8B762Q46938930-30CACE44-5EBF-485B-9C1A-0DFFA1BEC9AFQ46959456-D1C5A761-D32B-4338-A61F-1A141B5DADF6Q46982458-9E1ED452-5D5F-4819-B24A-404B7D0F11E1Q47334595-D23AAA8D-AC54-4EA9-8AC8-0A12B95EF23EQ48692705-73D6BEBC-F248-498C-B535-9BBB725538DBQ50222454-439F7535-596C-4904-9C23-4BB2E57B946EQ50247383-D16DA981-7396-405B-8FED-AAFEA60BA120Q50543188-F5C86D42-26D7-44F0-BBC3-E8672C882779Q50890288-47E4DC93-0049-4B1F-A304-8AC058F1A8D4Q50923516-C5F5D331-9BAC-477C-928B-233D5A07811DQ51070567-89510729-96E7-44D6-A078-EE5E48EDDA8DQ51071545-7AA16A1C-E16E-4A04-99DB-889D4304D0E4Q51128081-B7A78A83-BF0D-4EEF-ACF1-619969F4E7BCQ51185526-AB3305CD-7E71-4CCE-8A1C-957484CAE4ADQ51236805-807C01C4-9428-4E9E-AB8E-49A16FFDD6E7Q51244518-164BA46C-A5E7-4B5F-8A9B-6B983BB6BAAA
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Kazuo Takimiya
@ast
Kazuo Takimiya
@en
Kazuo Takimiya
@es
Kazuo Takimiya
@nl
Kazuo Takimiya
@sl
type
label
Kazuo Takimiya
@ast
Kazuo Takimiya
@en
Kazuo Takimiya
@es
Kazuo Takimiya
@nl
Kazuo Takimiya
@sl
prefLabel
Kazuo Takimiya
@ast
Kazuo Takimiya
@en
Kazuo Takimiya
@es
Kazuo Takimiya
@nl
Kazuo Takimiya
@sl
P1053
A-5841-2010
P106
P21
P31
P3829
P496
0000-0002-6001-1129
P569
2000-01-01T00:00:00Z