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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.
inferredcites →https://doi.org/10.1002/adma.200801650openalex-snapshotSemiconducting Thienothiophene Copolymers: Design, Synthesis, Morphology, and Performance in Thin‐Film Organic Transistors
inferredcites →https://doi.org/10.1002/adma.200802031openalex-snapshotDithieno[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
inferredcites →https://doi.org/10.1021/cr8004229openalex-snapshotFunctional Oligothiophenes: Molecular Design for Multidimensional Nanoarchitectures and Their Applications
inferredcites →https://doi.org/10.1021/ja964229jopenalex-snapshotInteraction of Oxygen with Conjugated Polymers: Charge Transfer Complex Formation with Poly(3-alkylthiophenes)
inferredcites →https://doi.org/10.1021/ma0488111openalex-snapshotSupramolecular Ordering, Thermal Behavior, and Photophysical, Electrochemical, and Electroluminescent Properties of Alkoxy-Substituted Yne-Containing Poly(phenylene−vinylene)s
inferredcites →https://doi.org/10.1021/ma702073mopenalex-snapshotDialkyl-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-snapshotPoly(3,6-dihexyl-thieno[3,2-b]thiophene vinylene): Synthesis, Field-Effect Transistors, and Photovoltaic Properties
inferredcites →https://doi.org/10.1021/ol9010745openalex-snapshotFacile and Scalable Synthesis of the Fused-Ring Heterocycles Thieno[3,2-b]thiophene and Thieno[3,2-b]furan
inferredcites →https://doi.org/10.1038/44359openalex-snapshotTwo-dimensional charge transport in self-organized, high-mobility conjugated polymers
inferredcites →https://doi.org/10.1039/a701877kopenalex-snapshotThienothiophenes. Part 2.1 Synthesis, metallation and bromine→lithium exchange reactions of thieno[3,2-b]thiophene and its polybromo derivatives
inferredcites →https://doi.org/10.1039/b301149fopenalex-snapshotLinearly extended tetrathiafulvalene analogues with fused thiophene units as π-conjugated spacers
inferredcites →https://doi.org/10.1039/b407794fopenalex-snapshotPhotovoltaic action of conjugated polymer/fullerene bulk heterojunction solar cells using novel PPE-PPV copolymers
inferredcites →https://doi.org/10.1039/b415481aopenalex-snapshot3,4-Ethylenedioxythiophene (EDOT) as a versatile building block for advanced functional π-conjugated systems
inferredcites →https://doi.org/10.3390/10010279openalex-snapshotChemical 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.
inferred← citeshttps://doi.org/10.1002/aoc.3325openalex-snapshotGreen synthesis of palladium nanoparticles using Pistacia atlantica kurdica gum and their catalytic performance in Mizoroki–Heck and Suzuki–Miyaura coupling reactions in aqueous solutions
inferred← citeshttps://doi.org/10.1002/aoc.3711openalex-snapshotIron oxide nanoparticles coated with green tea extract as a novel magnetite reductant and stabilizer sorbent for silver ions: Synthetic application of Fe3O4@green tea/Ag nanoparticles as magnetically separable and reusable nanocatalyst for reduction of 4‐nitrophenol
inferred← citeshttps://doi.org/10.1002/aoc.3737openalex-snapshotSilver nanoparticle‐decorated multiwalled carbon nanotube/pramipexole nanocomposite: Synthesis, characterization and application as an antibacterial agent
inferred← citeshttps://doi.org/10.1002/asia.201402925openalex-snapshotDiindolo[2,3‐b:2′,3′‐f]pyrrolo[3,2‐b]pyrroles as Electron‐Rich, Ladder‐Type Fluorophores: Synthesis and Optical Properties
inferred← citeshttps://doi.org/10.1002/bio.4640openalex-snapshotNew pyrrolo[3,2‐b]pyrroles with AIE characteristics for detection of dichloromethane and chloroform
inferred← citeshttps://doi.org/10.1002/pol.20200398openalex-snapshotPhotoinduced 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-snapshotCopolymers of 4‐thieno[3,2‐b]thiophen‐3‐ylbenzonitrile with anthracene and biphenyl; synthesis, characterization, electronic, optical, and thermal properties
inferred← citeshttps://doi.org/10.1007/s10562-016-1963-7openalex-snapshotSchiff 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-snapshotWITHDRAWN: 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.cattod.2017.04.033openalex-snapshotWITHDRAWN: CuI catalyst heterogenized on melamine-pyridines immobilized SBA-15: Heterogeneous and recyclable nanocatalyst for Ullmann-type C-N coupling reactions
inferred← citeshttps://doi.org/10.1016/j.cattod.2017.04.040openalex-snapshotWITHDRAWN: 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.dyepig.2017.08.056openalex-snapshotImproved synthesis of tetraaryl-1,4-dihydropyrrolo[3,2-b]pyrroles a promising dye for organic electronic devices: An experimental and theoretical approach
inferred← citeshttps://doi.org/10.1016/j.eurpolymj.2023.112028openalex-snapshotSynthesis, Photophysical properties and OFET application of thienothiophene and benzothiadiazole based Donor-π-Acceptor-π (D-π -A-π) type conjugated polymers
inferred← citeshttps://doi.org/10.1016/j.jcis.2017.02.023openalex-snapshotPreparation of core/shell nanostructure Fe3O4@PEG400-SO3H as heterogeneous and magnetically recyclable nanocatalyst for one-pot synthesis of substituted pyrroles by Paal-Knorr reaction at room temperature
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123250openalex-snapshotBio-supported of silver nanoparticles over magnetic nanoparticles: Assessmentof its catalytic reaction for the propargylamines synthesis and study of its antioxidant and anti-colon cancer consequences
inferred← citeshttps://doi.org/10.1016/j.polymer.2020.122954openalex-snapshotSurface characterization, electrochromic and capacitive properties of poly(N-(4-(4-thieno[3,2-b]thiophen-3-yl-phenyl)phenyl)-N-phenylbenzenamine) film
inferred← citeshttps://doi.org/10.1016/j.tet.2013.08.008openalex-snapshotWITHDRAWN: One-pot three-component synthesis of pyrano[3,2-d]isoxazoles catalyzed by N,N,N,N-tetramethylguanidinium formate [TMG][HCO2] as mild basic ionic liquid under mild conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.10.012openalex-snapshotCuI catalyst heterogenized on melamine-pyridines immobilized SBA-15: Heterogeneous and recyclable nanocatalyst for Ullmann-type C N coupling reactions
inferred← citeshttps://doi.org/10.1021/acs.jpcb.1c09448openalex-snapshotTriphenylamine/4,4′-Dimethoxytriphenylamine-Functionalized Thieno[3,2-b]thiophene Fluorophores with a High Quantum Efficiency: Synthesis and Photophysical Properties
inferred← citeshttps://doi.org/10.1021/acssuschemeng.1c07240openalex-snapshotTriphenylamine/Tetraphenylethylene Substituted 4-Thieno[3,2-b]thiophen-3-ylbenzonitriles: Synthesis, Photophysical-Electronic Properties, and Applications
inferred← citeshttps://doi.org/10.1021/cr500271aopenalex-snapshotThienothiophenes, Dithienothiophenes, and Thienoacenes: Syntheses, Oligomers, Polymers, and Properties
inferred← citeshttps://doi.org/10.1039/c4ob00143eopenalex-snapshotQuadrupolar, emission-tunable π-expanded 1,4-dihydropyrrolo[3,2-b]pyrroles – synthesis and optical properties
inferred← citeshttps://doi.org/10.1039/c4ra14668aopenalex-snapshotPalladium nanoparticles supported on 1,3-dicyclohexylguanidine functionalized mesoporous silica SBA-15 as highly active and reusable catalyst for the Suzuki–Miyaura cross-coupling reaction
inferred← citeshttps://doi.org/10.1039/c4ra14964eopenalex-snapshotSelective hydrogen peroxide oxidation of sulfides to sulfones with carboxylated multi-walled carbon nano tubes (MWCNTs-COOH) as heterogeneous and recyclable nanocatalysts under organic solvent-free conditions
inferred← citeshttps://doi.org/10.1039/c6gc01975gopenalex-snapshotPreparation of polydopamine sulfamic acid-functionalized magnetic Fe 3 O 4 nanoparticles with a core/shell nanostructure as heterogeneous and recyclable nanocatalysts for the acetylation of alcohols, phenols, amines and thiols under solvent-free conditions
inferred← citeshttps://doi.org/10.1039/c6tc01285jopenalex-snapshotNovel organoboron compounds derived from thieno[3,2-b]thiophene and triphenylamine units for OLED devices
inferred← citeshttps://doi.org/10.1039/c9ra08023fopenalex-snapshotConcise synthesis of 3-alkylthieno[3,2- b ]thiophenes; building blocks for organic electronic and optoelectronic materials
inferred← citeshttps://doi.org/10.1039/d0tc01715aopenalex-snapshotTetraphenylethylene substituted thienothiophene and dithienothiophene derivatives: synthesis, optical properties and OLED applications
inferred← citeshttps://doi.org/10.1039/d2ra05768aopenalex-snapshotDithieno[3,2- b :2′,3′- d ]thiophene (DTT): an emerging heterocyclic building block for future organic electronic materials & functional supramolecular chemistry
inferred← citeshttps://doi.org/10.1039/d2tc01222gopenalex-snapshotHigh-performance, low-voltage organic field-effect transistors using thieno[3,2- b ]thiophene and benzothiadiazole co-polymers
inferred← citeshttps://doi.org/10.1039/d2tc02371gopenalex-snapshotSolution-processable donor–π–acceptor type thieno[3,2- b ]thiophene derivatives; synthesis, photophysical properties and applications
inferred← citeshttps://doi.org/10.3390/org5040027openalex-snapshotSynthesis of Thieno[3,2-b]thiophenes from 2,5-Dicarbonyl 3-Nitrothiophenes via Nucleophilic Aromatic Substitution of the Nitro Group with Thiolates
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