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Accelerated Intramolecular Charge Transfer in Tetracyanobutadiene- and Expanded Tetracyanobutadiene-Incorporated Asymmetric Triphenylamine–Quinoxaline Push–Pull Conjugates
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Organic Nanomaterials: Synthesis, Characterization, and Device Applications
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Dibenzothiophene/Oxide and Quinoxaline/Pyrazine Derivatives Serving as Electron‐Transport Materials
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Triphenylamine Functionalized Unsymmetrical Quinoxalines
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Charge‐Transfer Chromophores by Cycloaddition–Retro‐electrocyclization: Multivalent Systems and Cascade Reactions
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Optical Stability of Axially Chiral Push–Pull‐Substituted Buta‐1,3‐dienes: Effect of a Single Methyl Group on the C60 Surface
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Intense Ground‐State Charge‐Transfer Interactions in Low‐Bandgap, Panchromatic Phthalocyanine–Tetracyanobuta‐1,3‐diene Conjugates
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Strong Ground‐ and Excited‐State Charge Transfer in C3‐Symmetric Truxene‐Derived Phenothiazine‐Tetracyanobutadine and Expanded Conjugates
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Interfacing High‐Energy Charge‐Transfer States to a Near‐IR Sensitizer for Efficient Electron Transfer upon Near‐IR Irradiation
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Photoinduced Charge Separation Prompted Intervalence Charge Transfer in a Bis(thienyl)diketopyrrolopyrrole Bridged Donor‐TCBD Push‐Pull System
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Red‐Light‐Emitting System Based on Aggregation of Donor–Acceptor Derivatives in Polar Aqueous Media
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Property Tuning in Charge‐Transfer Chromophores by Systematic Modulation of the Spacer between Donor and Acceptor
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Ultrafast Charge‐Separation in Triphenylamine‐BODIPY‐Derived Triads Carrying Centrally Positioned, Highly Electron‐Deficient, Dicyanoquinodimethane or Tetracyanobutadiene Electron‐Acceptors
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Excited‐State Electron Transfer in 1,1,4,4‐Tetracyanobuta‐1,3‐diene (TCBD)‐ and Cyclohexa‐2,5‐diene‐1,4‐diylidene‐Expanded TCBD‐Substituted BODIPY‐Phenothiazine Donor–Acceptor Conjugates
inferredcites →https://doi.org/10.1002/chem.202200348openalex-snapshot
Near‐IR Intramolecular Charge Transfer in Strongly Interacting Diphenothiazene‐TCBD and Diphenothiazene‐DCNQ Push‐Pull Triads
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Donor‐Substituted 1,1,4,4‐Tetracyanobutadienes (TCBDs): New Chromophores with Efficient Intramolecular Charge‐Transfer Interactions by Atom‐Economic Synthesis.
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Reactions between 1‐Ethynylazulenes and 7,7,8,8‐Tetracyanoquinodimethane (TCNQ): Preparation, Properties, and Redox Behavior of Novel Azulene‐Substituted Redox‐Active Chromophores
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Kinetics of Fluorescence Quenching by Electron and H‐Atom Transfer
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Design and photochemical study of supramolecular donor–acceptor systems assembled via metal–ligand axial coordination
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Synthesis and fluorescent properties of quinoxaline derived ionic liquids
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Novel Y-shaped AIEE-TICT active π-extended quinoxalines-based donor–acceptor molecules displaying acidofluorochromism and temperature dependent emission
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Synthesis and optical properties of bipolar quinoxaline-triphenylamine based stilbene compounds
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Radiative electron transfer in planar donor–acceptor quinoxaline derivatives
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Symmetric and Asymmetric Push–Pull Conjugates: Significance of Pull Group Strength on Charge Transfer and Separation
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Conversion of Large-Bandgap Triphenylamine–Benzothiadiazole to Low-Bandgap, Wide-Band Capturing Donor–Acceptor Systems by Tetracyanobutadiene and/or Dicyanoquinodimethane Insertion for Ultrafast Charge Separation
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Long-Lived Charge Separation and Applications in Artificial Photosynthesis
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Large π-Aromatic Molecules as Potential Sensitizers for Highly Efficient Dye-Sensitized Solar Cells
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Quinoxalines Incorporating Triarylamines: Potential Electroluminescent Materials with Tunable Emission Characteristics
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Chromophore-Labeled Quinoxaline Derivatives as Efficient Electroluminescent Materials
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Structural−Property Relationship in Pyrazino[2,3-g]quinoxaline Derivatives: Morphology, Photophysical, and Waveguide Properties
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Covalent and Noncovalent Phthalocyanine−Carbon Nanostructure Systems: Synthesis, Photoinduced Electron Transfer, and Application to Molecular Photovoltaics
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Subphthalocyanines Axially Substituted with a Tetracyanobuta-1,3-diene–Aniline Moiety: Synthesis, Structure, and Physicochemical Properties
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Controlling the Charge Transfer in D–A–D Chromophores Based on Pyrazine Derivatives
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Triphenylamine-modified quinoxaline derivatives as two-photon photoinitiators
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Unprecedented thermal rearrangement of push–pull-chromophore–[60]fullerene conjugates: formation of chiral 1,2,9,12-tetrakis-adducts
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Realizing artificial photosynthesis
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Bidirectional charge-transfer behavior in carbon-based hybrid nanomaterials
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Glotaran : A Java -Based Graphical User Interface for the R Package TIMP
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Zinc Tetrapyrrole Coordinated to Imidazole Functionalized Tetracyanobutadiene or Cyclohexa‐2,5‐diene‐1,4‐diylidene‐expanded‐tetracyanobutadiene Conjugates: Dark vs. Light‐Induced Electron Transfer
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Unique structural effect on the fluorosolvatochromism and dual fluorescence emission of D-π-A+ cationic chromophores with furyl bridge. An approach to white light emitters
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Near infrared absorbing derivatives of triphenylamine containing 1,1,4,4-tetracyanobutadiene or dicyanoquinodimethane moieties for fast responsive solitary and binary organic photodetectors
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Synthesis of Nonplanar Push–Pull Chromophores with Various Heterocyclic Moieties via [2 + 2] Cycloaddition-Retroelectrocyclization Reaction
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Synthesis and Understanding of the Role of Donor-Tetracyanobutadiene in Porphyrin β-Periphery toward Ultrafast Charge Transfer Dynamics
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Tetracyanobutadiene- and Dicyanoquinodimethane-Benzothiadiazole Push–Pull Systems: The Role of Terminal Electron Donors in Governing Intramolecular Charge Transfer
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Perylenediimide promoted charge transfer in tetracyano butadiene–triphenylamine (TCBD–TPA) and expanded-tetracyano butadiene–triphenylamine (DCNQ–TPA) push–pull conjugates
inferred← citeshttps://doi.org/10.1039/d6dt01578fopenalex-snapshot
Y-shaped quinoxaline-based chiral and racemic ferrocene naphthalimides for enhanced second harmonic generation and circularly polarized luminescence
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Photoinduced energy transfer in sulfur-based heterocyclic compounds and corrole dyads
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Theoretical Study of Copper Squarate as a Promising Adsorbent for Small Gases Pollutants
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