Works matching DE "TRIPHENYLAMINE"
Results: 594
Fluorescence emission modification of triphenylamine derivatives by aggregate formation in solution or by mechanical stress in solid state.
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- Emergent Scientist, 2024, v. 8, p. 1, doi. 10.1051/emsci/2023004
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Caulerpa lentillifera Seaweed Extract as Natural Sensitizer for Dye‐Sensitized Solar Cell.
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- Macromolecular Symposia, 2023, v. 407, n. 1, p. 1, doi. 10.1002/masy.202100359
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Exploring the impact of tailored π-linkers on perovskite solar cell efficiency: a computational study in triphenylamine-based hole transport material design.
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- Optical & Quantum Electronics, 2024, v. 56, n. 6, p. 1, doi. 10.1007/s11082-024-06902-w
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Theoretical insights into metal-free oligothiophene-centered dye with A–D–A framework via end group modification for DSSCs.
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- Optical & Quantum Electronics, 2024, v. 56, n. 6, p. 1, doi. 10.1007/s11082-024-06802-z
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Structural, photophysical and optoelectronic activity of triphenylamine-based push–pull chromophores: a theoretical study.
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- Optical & Quantum Electronics, 2022, v. 54, n. 12, p. 1, doi. 10.1007/s11082-022-04239-w
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Design and theoretical study of phenothiazine-based low bandgap dye derivatives as sensitizers in molecular photovoltaics.
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- Optical & Quantum Electronics, 2020, v. 52, n. 11, p. N.PAG, doi. 10.1007/s11082-020-02600-5
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Computational analysis on D–π–A based perylene organic efficient sensitizer in dye-sensitized solar cells.
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- Optical & Quantum Electronics, 2020, v. 52, n. 3, p. 1, doi. 10.1007/s11082-020-02273-0
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Quantum chemical study of the effect of π-bridge on the optical and electronic properties of sensitizers for DSSCs incorporating dioxythiophene and thiophene units.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2016, v. 135, n. 10, p. 1, doi. 10.1007/s00214-016-1989-3
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Predicting light absorption properties of anthocyanidins in solution: a multi-level computational approach.
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- Theoretical Chemistry Accounts: Theory, Computation, & Modeling, 2016, v. 135, n. 6, p. 1, doi. 10.1007/s00214-016-1911-z
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Novel thiophene-containing push-pull chromophores that include carbazole and triphenylamine moieties: study of optical and electrochemical properties.
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- Chemistry of Heterocyclic Compounds, 2016, v. 52, n. 6, p. 379, doi. 10.1007/s10593-016-1899-2
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2-amino-5-aryl- and 2-amino-5-hetaryl-3-cyano-6-(2-thienyl)pyridines as Organic Dyes for Dye-Sensitized Solar Cells: Synthesis, Quantum-Chemical Calculations, Spectral and Electrochemical Properties.
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- Chemistry of Heterocyclic Compounds, 2014, v. 50, n. 6, p. 814, doi. 10.1007/s10593-014-1536-x
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Photovoltaic Molecule Containing Bi-4-Hexyl-Thienylenevinylene(BHTV)as the Conjugated Pi-Bridge for Bulk-Heterojunction Organic Solar Cells.
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- Journal of Changzhou University (Natural Science Edition) / Changzhou Daxue Xuebao (Ziran Kexue Ban), 2018, v. 30, n. 6, p. 17, doi. 10.3969/j.issn.2095-0411.2018.06.003
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Can A Double-Doped Device Modification of A Standard Bilayer OLED Improve the Photo- And/or Electro-luminescence Efficiency? A Case Study of Architecture Design in Fluorescent Devices with A Potential Roadmap for High-Efficiency Phosphorescent Devices.
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- Comments on Inorganic Chemistry, 2022, v. 42, n. 3, p. 145, doi. 10.1080/02603594.2021.1992399
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New conjugated electroluminescent triphenylamine-containing polymers with side-chain pyridin-2-ylimidazo[1,5- a]pyridine groups for polymer light-emitting diodes.
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- Doklady Chemistry, 2013, v. 450, n. 2, p. 165, doi. 10.1134/S0012500813060050
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Research progress of triphenylamine dye sensitizers of solar cells.
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- Journal of Hebei University of Science & Technology, 2015, v. 36, n. 2, p. 210, doi. 10.7535/hbkd.2015yx02015
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Effect of natural dye combination and pH extraction on the performance of dye-sensitized photovoltaics solar cell.
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- International Journal of Renewable Energy Development, 2023, v. 12, n. 6, p. 1054, doi. 10.14710/ijred.2023.56172
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Solution-processed deep-blue (y∼0.06) fluorophores based on triphenylamine-imidazole (donor-acceptor) for OLEDs: computational and experimental exploration.
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- Journal of Information Display, 2022, v. 23, n. 1, p. 53, doi. 10.1080/15980316.2021.1959429
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Interfaces and pattern resolution of inkjet-printed organic light-emitting diodes with a novel hole transport layer.
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- Journal of Information Display, 2021, v. 22, n. 2, p. 91, doi. 10.1080/15980316.2020.1866090
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Electrochemical and spectrophotometric properties of polymers based on derivatives of di- and triphenylamines as promising materials for electronic applications.
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- Designed Monomers & Polymers, 2015, v. 18, n. 8, p. 770, doi. 10.1080/15685551.2015.1078110
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Synthesis, properties, and self-polymerization of hole-transporting carbazole- and triphenylamine-based hydrazone monomers.
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- Designed Monomers & Polymers, 2014, v. 17, n. 3, p. 255, doi. 10.1080/15685551.2013.840499
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Linear and hyperbranched triphenylamine-based polyarylenevinylenes: a comparative optoelectronic study.
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- Designed Monomers & Polymers, 2014, v. 17, n. 2, p. 156, doi. 10.1080/15685551.2013.840495
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Synthesis and study of optical properties of linear and hyperbranched conjugated polymers containing thiophene and triphenylamine units.
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- Designed Monomers & Polymers, 2014, v. 17, n. 1, p. 7, doi. 10.1080/15685551.2013.771313
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Observation of aligned dipoles and angular chromism of exciplexes in organic molecular heterostructures.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-42976-y
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The host–guest inclusion driven by host-stabilized charge transfer for construction of sequentially red-shifted mechanochromic system.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39956-7
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Effect of Exchange-correlation Functionals on Ground State Geometries, Optoelectronic and Charge Transfer of Triphenylamine-based Dyes.
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- Orbital: The Electronic Journal of Chemistry, 2022, v. 14, n. 1, p. 45, doi. 10.17807/orbital.v14i1.1682
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Leishmaniasis Cutánea, Reconstrucción 3D, ulcera, seguimiento.
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- Óptica Pura y Aplicada, 2022, v. 55, n. 1, p. 1, doi. 10.7149/OPA.55.1.51085
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Synthesis, self-assembly and photophysical properties of AIEE-active triphenylamine-based discotic liquid crystals.
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- Journal of the Iranian Chemical Society, 2022, v. 19, n. 11, p. 4411, doi. 10.1007/s13738-022-02611-x
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Acceptor substituent effect on triphenylamine-based organic dye sensitizers for DSSCs: quantum chemical study.
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- Journal of the Iranian Chemical Society, 2021, v. 18, n. 6, p. 1279, doi. 10.1007/s13738-020-02112-9
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Design, synthesis of organic sensitizers containing carbazole and triphenylamine π-bridged moiety for dye-sensitized solar cells.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 9, p. 1923, doi. 10.1007/s13738-019-01663-w
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The Effect of TCNE and TCNQ Acceptor Units on Triphenylamine-Naphthalenediimide Push-Pull Chromophore Properties.
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- European Journal of Organic Chemistry, 2021, v. 2021, n. 18, p. 2615, doi. 10.1002/ejoc.202100198
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Reversible Addition of Cyanide to Triphenylamine Attached Difluoroboron β‐Diketonate Facilitated Selective Colorimetric and Fluorimetric Detection of Cyanide Ion.
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- European Journal of Organic Chemistry, 2020, v. 2020, n. 8, p. 993, doi. 10.1002/ejoc.201901820
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Influence of Donor‐Substituents on Triphenylamine Chromophores Bearing Pyridine Fragments.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 9, p. 1921, doi. 10.1002/ejoc.201900026
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Manipulation of Donor-Acceptor Interactions in Carbazole-Based Emitters by Chromophore Choice To Achieve Near-UV Emission.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 45, p. 6660, doi. 10.1002/ejoc.201701285
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Toward Sustainable Organic Semiconductors from a Broad Palette of Green Reactions.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 19, p. 2707, doi. 10.1002/ejoc.201700317
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Starburst Triphenylamine-Based Donor-Acceptor-Type Small Molecules for Solution-Processed Organic Solar Cells.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 4, p. 799, doi. 10.1002/ejoc.201501376
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N-Substituted Dicyanomethylphenyl Radicals: Dynamic Covalent Properties and Formation of Stimuli-Responsive Cyclophanes by Self-Assembly.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 30, p. 8634, doi. 10.1002/anie.201603409
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Evidence for Interfacial Halogen Bonding.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 20, p. 5956, doi. 10.1002/anie.201510641
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Pyridyl Pyrrolide Boron Complexes: The Facile Generation of Thermally Activated Delayed Fluorescence and Preparation of Organic Light-Emitting Diodes.
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- Angewandte Chemie International Edition, 2016, v. 55, n. 9, p. 3017, doi. 10.1002/anie.201509231
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ATriphenylamine with Two Phenoxy Radicals Having Unusual Bonding Patterns and a Closed-Shell Electronic State.
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- Angewandte Chemie International Edition, 2015, v. 54, n. 28, p. 8267, doi. 10.1002/anie.201502949
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Fluorene-based conjugates with geminal donor-acceptor: synthesis, photophysical properties and theoretical studies.
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- Journal of Chemical Sciences, 2024, v. 136, n. 2, p. 1, doi. 10.1007/s12039-024-02249-7
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Novel ternary exciplex system based on TCTA dendrimer with a new linking type amongst various functional donors.
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- Journal of Materials Science: Materials in Electronics, 2022, v. 33, n. 14, p. 11403, doi. 10.1007/s10854-022-08113-z
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Imidazo[1,2-a]pyridine based deep-blue emitter: effect of donor on the optoelectronic properties.
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- Journal of Materials Science: Materials in Electronics, 2021, v. 32, n. 22, p. 26838, doi. 10.1007/s10854-021-07060-5
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Studies on photophysical and electrochemical properties of triphenylamine α, β-unsaturated ketone side-arm PAE CPs.
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- Journal of Materials Science: Materials in Electronics, 2021, v. 32, n. 9, p. 11426, doi. 10.1007/s10854-021-05505-5
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A scalable synthesis of carbon nanotube ink for Pad-dry-deposition method for solar cell application.
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- Journal of Materials Science: Materials in Electronics, 2021, v. 32, n. 5, p. 6123, doi. 10.1007/s10854-021-05330-w
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Synthesis of a Novel Dinuclear Ruthenium(III) Ono Pincer Complex Containing a M–M Bond: an XRD Study.
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- Journal of Structural Chemistry, 2023, v. 64, n. 11, p. 2082, doi. 10.1134/S0022476623110057
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Coordination Polymers Constructed from the 3,3′,5,5′-Biphenyltetracarboxylic Acid Ligand and Their Application for Anti-Lung Cancer Reagents.
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- Journal of Structural Chemistry, 2020, v. 61, n. 5, p. 789, doi. 10.1134/S0022476620050157
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Studies of Carbon Dioxide Capture on Porous Chitosan Derivative.
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- Journal of Dispersion Science & Technology, 2016, v. 37, n. 2, p. 155, doi. 10.1080/01932691.2015.1035388
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Estimation of Imatinib in pure and pharmaceutical forms using triphenyl methane dyes.
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- International Journal of Pharmaceutical Research (09752366), 2018, v. 10, n. 2, p. 167
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Triphenylamine-Based Solid-State Emissive Fluorene Derivative with Aggregation-Induced Emission Enhancement Characteristics.
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- Celal Bayar University Journal of Science, 2024, v. 20, n. 3, p. 100, doi. 10.18466/cbayarfbe.1516889
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A Novel Donor-π-Acceptor Type Sensitizer for Dye Sensitized Photochemical Hydrogen Generation.
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- Celal Bayar University Journal of Science, 2021, v. 17, n. 2, p. 167, doi. 10.18466/cbayarfbe.844704
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