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Concise Syntheses, Polymers, and Properties of 3-Arylthieno[3,2-b]thiophenes

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1 of the 41 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1126/science.289.5479.599 (notice 2002-11-01).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Plastic Solar Cells
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Light‐Emitting Polythiophenes
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Semiconducting Thienothiophene Copolymers: Design, Synthesis, Morphology, and Performance in Thin‐Film Organic Transistors
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Dithieno[2,3‐d;2′,3′‐d′]benzo[1,2‐b;4,5‐b′]dithiophene (DTBDT) as Semiconductor for High‐Performance, Solution‐Processed Organic Field‐Effect Transistors
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Molecular Engineering of the Band Gap of π‐Conjugated Systems: Facing Technological Applications
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Reductive degradation of nitrobenzene in aqueous solution by zero-valent iron
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From thiophene to Sulflower
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Dithienothiophenes
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A new reaction of P4S10 and Lawesson's reagent; a new method for the synthesis of dithieno[3,2-b;2′,3′-d]thiophenes
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Rigid oligomers based on the combination of 3,6-dimethoxythieno[3,2-b]thiophene and 3,4-ethylenedioxythiophene
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Materials and Devices toward Fully Solution Processable Organic Light-Emitting Diodes
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Conjugated poly(thiophenes): synthesis, functionalization, and applications
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Functional Oligothiophenes: Molecular Design for Multidimensional Nanoarchitectures and Their Applications
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A Berzelius Reagent, Phosphorus Decasulfide (P4S10), in Organic Syntheses
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Ultrathin Organic Films Grown by Organic Molecular Beam Deposition and Related Techniques
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Synthetic Principles for Bandgap Control in Linear π-Conjugated Systems
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Alkylsubstituted Thienothiophene Semiconducting Materials: Structure−Property Relationships
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Interaction of Oxygen with Conjugated Polymers: Charge Transfer Complex Formation with Poly(3-alkylthiophenes)
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Supramolecular Ordering, Thermal Behavior, and Photophysical, Electrochemical, and Electroluminescent Properties of Alkoxy-Substituted Yne-Containing Poly(phenylene−vinylene)s
inferredcites →https://doi.org/10.1021/ma049107nopenalex-snapshot
Alkyl-Substituted Thieno[3,2-b]thiophene Polymers and Their Dimeric Subunits
inferredcites →https://doi.org/10.1021/ma702073mopenalex-snapshot
Dialkyl-Substituted Thieno[3,2-b]thiophene-Based Polymers Containing 2,2‘-Bithiophene, Thieno[3,2-b]thiophene, and Ethynylene Spacers
inferredcites →https://doi.org/10.1021/ma801923copenalex-snapshot
Poly(3,6-dihexyl-thieno[3,2-b]thiophene vinylene): Synthesis, Field-Effect Transistors, and Photovoltaic Properties
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Facile and Scalable Synthesis of the Fused-Ring Heterocycles Thieno[3,2-b]thiophene and Thieno[3,2-b]furan
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Light-emitting diodes with variable colours from polymer blends
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Two-dimensional charge transport in self-organized, high-mobility conjugated polymers
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Thienothiophenes. Part 2.1 Synthesis, metallation and bromine→lithium exchange reactions of thieno[3,2-b]thiophene and its polybromo derivatives
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Linearly extended tetrathiafulvalene analogues with fused thiophene units as π-conjugated spacers
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Photovoltaic action of conjugated polymer/fullerene bulk heterojunction solar cells using novel PPE-PPV copolymers
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3,4-Ethylenedioxythiophene (EDOT) as a versatile building block for advanced functional π-conjugated systems
inferredcites →https://doi.org/10.1039/b417803nopenalex-snapshot
Scientific importance, properties and growing applications of poly(3,4-ethylenedioxythiophene)
inferredcites →https://doi.org/10.1039/b900979eopenalex-snapshot
Thieno[3,2-b]thiophene oligomers and their applications as p-type organic semiconductors
inferredcites →https://doi.org/10.1039/c1jm10406copenalex-snapshot
Fluorescence and visual sensing of nitroaromatic explosives using electron rich discrete fluorophores
inferredcites →https://doi.org/10.1063/1.125387openalex-snapshot
Polymer diodes with high rectification
inferredcites →https://doi.org/10.1063/1.98799openalex-snapshot
Organic electroluminescent diodes
inferredcites →https://doi.org/10.1070/rc2005v074n03abeh000889openalex-snapshot
The latest achievements in thienothiophene chemistry
inferredcites →https://doi.org/10.1126/science.289.5479.599openalex-snapshot
An Organic Solid State Injection Laser
inferredcites →https://doi.org/10.2174/1570193043403118openalex-snapshot
Thienothiophenes: Synthesis and Applications
inferredcites →https://doi.org/10.3390/10010279openalex-snapshot
Chemical and Photochemical Synthesis of Substituted Dihydro-thieno[2',3':4,5]thieno[2,3-c]quinolin-6-ones and Tetrahydro-dithieno[2,3-b:2',3'-d]thieno[2'',3''c:2'',3''c’]diquinolin-6,14-dione

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1002/bio.4640openalex-snapshot
New pyrrolo[3,2‐b]pyrroles with AIE characteristics for detection of dichloromethane and chloroform
inferred← citeshttps://doi.org/10.1002/chem.201501401openalex-snapshot
Reversible Doping of a Dithienothiophene‐Based Conjugated Microporous Polymer
inferred← citeshttps://doi.org/10.1002/chem.201505052openalex-snapshot
Z‐Shaped Pyrrolo[3,2‐b]pyrroles and Their Transformation into π‐Expanded Indolo[3,2‐b]indoles
inferred← citeshttps://doi.org/10.1002/cplu.201700158openalex-snapshot
Pyrrolo[3,2‐b]pyrrole as the Central Core of the Electron Donor for Solution‐Processed Organic Solar Cells
inferred← citeshttps://doi.org/10.1002/ejoc.201600806openalex-snapshot
Synthesis, Fluorescence, and Two‐Photon Absorption Properties of Push–Pull 5‐Arylthieno[3,2‐b]thiophene Derivatives
inferred← citeshttps://doi.org/10.1002/pol.20200398openalex-snapshot
Photoinduced step‐growth polymerization of thieno[3,4‐b] thiophene derivatives. The substitution effect on the reactivity and electrochemical properties
inferred← citeshttps://doi.org/10.1002/pol.20200635openalex-snapshot
Copolymers of 4‐thieno[3,2‐b]thiophen‐3‐ylbenzonitrile with anthracene and biphenyl; synthesis, characterization, electronic, optical, and thermal properties
inferred← citeshttps://doi.org/10.1002/slct.201600697openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/slct.201700174openalex-snapshot
White Light Emitting Polymers Possessing Thienothiophene and Boron Units
inferred← citeshttps://doi.org/10.1002/slct.202003273openalex-snapshot
A Bifunctional Bulky Thienothiophene Derivative; Synthesis, Electronic‐Optical Properties and OLED Applications
inferred← citeshttps://doi.org/10.1007/7081_2014_129openalex-snapshot
Fused Thiophenes and Some Oligomers and Polymers Therefrom
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Phosphorus Pentasulfide in Heterocycle Synthesis
inferred← citeshttps://doi.org/10.1007/s10562-016-1963-7openalex-snapshot
Schiff Base-Functionalized Multi Walled Carbon Nano Tubes to Immobilization of Palladium Nanoparticles as Heterogeneous and Recyclable Nanocatalyst for Suzuki Reaction in Aqueous Media Under Mild Conditions
inferred← citeshttps://doi.org/10.1016/j.cattod.2017.04.028openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cattod.2017.04.033openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cattod.2017.04.040openalex-snapshot
WITHDRAWN: Multi walled carbon nanotubes modified with mercapto-melamine groups for the stabilization of palladium nanoparticles: An efficient nanocatalyst for the Suzuki reaction in aqueous media under mild conditions
inferred← citeshttps://doi.org/10.1016/j.cej.2021.133868openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.dyepig.2017.08.056openalex-snapshot
Improved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
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Synthesis and Electropolymerization of Bis(phenylthieno[3,2-b]thiophenes)– (4,4'-dinonyl-2,2'-bithiazole) co-monomer
inferred← citeshttps://doi.org/10.1016/j.electacta.2016.12.153openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.electacta.2021.138688openalex-snapshot
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Synthesis and characterization of 3-(4-fluorophenyl)thieno[3,2-b]thiophene and 3,3’-(4- fluorophenyl)dithieno[3,2-b;2’,3’-d]thiophene molecules
inferred← citeshttps://doi.org/10.1016/j.electacta.2021.139020openalex-snapshot
Synthesis and optoelectronic and charge storage characterizations of conducting polymers based on tetraphenylethylene and thienothiophenes
inferred← citeshttps://doi.org/10.1016/j.est.2024.113272openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2018.05.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2022.111167openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2023.112028openalex-snapshot
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