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2,1,3‐Benzothiadiazole and Derivatives: Synthesis, Properties, Reactions, and Applications in Light Technology of Small Molecules

https://doi.org/10.1002/ejoc.201201161

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Benzothiadiazole-based Conjugated Polymers for Organic Solar Cells

inferred← citeshttps://doi.org/10.1007/s10593-015-1683-8openalex-snapshot

A short and safe method for the synthesis of [1,2,5]oxadiazolo[3,4-c] pyridine

inferred← citeshttps://doi.org/10.1007/s10593-017-2099-4openalex-snapshot

Suzuki cross-coupling reactions of 4,7-dibromo[1, 2, 5]selenadiazolo[3,4-c]pyridine – a path to new solar cell components

inferred← citeshttps://doi.org/10.1007/s10895-025-04703-2openalex-snapshot

Synthesis of 2-(3,5-diarylaminophenyl)-2h-benzo[d][1,2,3]triazoles With Aggregation Induced Emission Properties and Its Applications as a Blue OLED Component

inferred← citeshttps://doi.org/10.1007/s11082-021-03162-wopenalex-snapshot

Butterfly-shaped hole transport materials with outstanding photovoltaic properties for organic solar cells

inferred← citeshttps://doi.org/10.1007/s11101-023-09862-3openalex-snapshot

The effects of exogenously applied antioxidants on plant growth and resilience

inferred← citeshttps://doi.org/10.1007/s11172-022-3499-xopenalex-snapshot

Synthesis and crystal structure of a luminescent metal-organic framework based on 4,7-(4-carboxyphenyl)-2,1,3-benzoxadiazole

inferred← citeshttps://doi.org/10.1007/s11426-020-9901-4openalex-snapshot

Recent progress of electronic materials based on 2,1,3-benzothiadiazole and its derivatives: synthesis and their application in organic light-emitting diodes

inferred← citeshttps://doi.org/10.1007/s11998-025-01138-zopenalex-snapshot

Synthesis and purification of carbon dots from fluorescent precursors as colorant for fluorescent ink

inferred← citeshttps://doi.org/10.1007/s40010-016-0275-zopenalex-snapshot

Theoretical Design of Benzoselenadiazole Based Organic Donor Molecules for Solar Cell Applications

inferred← citeshttps://doi.org/10.1007/s40843-024-3197-3openalex-snapshot

A-D-A′-D-A-type non-fused ring electron acceptors for organic solar cells and photodetectors

inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14813-9openalex-snapshot

1,2,5-Thiadiazoles

inferred← citeshttps://doi.org/10.1016/bs.aihch.2015.04.002openalex-snapshot

The Literature of Heterocyclic Chemistry, Part XIII, 2012–2013

inferred← citeshttps://doi.org/10.1016/bs.aihch.2016.04.009openalex-snapshot

Heterocyclic Building Blocks for Organic Semiconductors

inferred← citeshttps://doi.org/10.1016/bs.aihch.2026.03.001openalex-snapshot

Hetero-antiaromatics: 1,3,2,4-Benzodithiadiazines and related compounds

inferred← citeshttps://doi.org/10.1016/j.bioorg.2018.12.025openalex-snapshot

Synthesis of novel quinoline-based thiadiazole, evaluation of their antileishmanial potential and molecular docking studies

inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104467openalex-snapshot

BODIPY based red emitters: Synthesis, computational and biological studies

inferred← citeshttps://doi.org/10.1016/j.bmc.2013.10.019openalex-snapshot

A novel nitro-substituted benzothiadiazole as fluorescent probe for tumor cells under hypoxic condition

inferred← citeshttps://doi.org/10.1016/j.ccr.2025.217410openalex-snapshot

Weak bonds-driven AIE and AIEE effects in benzothiadiazole derivatives: a critical review

inferred← citeshttps://doi.org/10.1016/j.ccr.2026.218213openalex-snapshot

Single-selenium-atom engineering: a rising strategy reshaping organic photosensitizers in photodynamic therapy

inferred← citeshttps://doi.org/10.1016/j.chroma.2013.10.075openalex-snapshot

Dithienyl benzothiadiazole derivatives: A new type of stationary phases for capillary gas chromatography

inferred← citeshttps://doi.org/10.1016/j.colsurfa.2024.134658openalex-snapshot

Designing strategically functionalized hybrid porous polymers with octavinylsilsesquioxane/dibenzo[g,p]chrysene/benzo[c]-1,2,5-thiadiazole units for rapid removal of Rhodamine B dye from water

inferred← citeshttps://doi.org/10.1016/j.dyepig.2016.10.005openalex-snapshot

Synthesis and properties of benzothiadiazole-pyridine system: The modulation of optical feature

inferred← citeshttps://doi.org/10.1016/j.dyepig.2017.08.055openalex-snapshot

Synthesis and properties of new benzothiadiazole-based push-pull dyes for p-type dye sensitized solar cells

inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.03.043openalex-snapshot

Influence of the structure of electron-donating aromatic units in organosilicon luminophores based on 2,1,3-benzothiadiazole electron-withdrawing core on their absorption-luminescent properties

inferred← citeshttps://doi.org/10.1016/j.dyepig.2018.12.012openalex-snapshot

Phase-dependent photoluminescence of non-symmetric 2,1,3-benzothiadiazole liquid crystals

inferred← citeshttps://doi.org/10.1016/j.dyepig.2020.108377openalex-snapshot

Designing highly luminescent aryloxy-benzothiadiazole derivatives with aggregation-induced enhanced emission

inferred← citeshttps://doi.org/10.1016/j.dyepig.2020.108668openalex-snapshot

Synthesis and thermal, electrochemical, and photophysical investigation of carbazole/diphenyl benzothiadiazole-based fluorophores

inferred← citeshttps://doi.org/10.1016/j.dyepig.2020.108703openalex-snapshot

Synthesis and photo-electro-thermal characterization of non-symmetrical 4,7-dibromobenzo[c][1,2,5]thiadiazole derivatives

inferred← citeshttps://doi.org/10.1016/j.dyepig.2020.109005openalex-snapshot

Plasma membrane staining with fluorescent hybrid benzothiadiazole and coumarin derivatives: Tuning the cellular selection by molecular design

inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109345openalex-snapshot

Expanding benzothiadiazole-tetrazole photo-triggered click reaction with chloride ion into reaction-based chloride ion receptor

inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110308openalex-snapshot

How to achieve near unity fluorescence quantum yields on gold(I) benzothiadiazole-based derivatives

inferred← citeshttps://doi.org/10.1016/j.dyepig.2022.110978openalex-snapshot

Mono-silylated 2,1,3-benzothiadiazole-based precursors. Molecular scaffolds for obtaining fluorescent organic-inorganic hybrid materials with tailored photophysical properties

inferred← citeshttps://doi.org/10.1016/j.dyepig.2023.111213openalex-snapshot

Polyaryl substituted imidazobenzothiadiazoles as multifunctional organic fluorescent materials for visualization of latent fingerprints and lysosome staining

inferred← citeshttps://doi.org/10.1016/j.dyepig.2023.111388openalex-snapshot

Intense millisecond-long red luminescence from heteroleptic Cu(I) 2,1,3-benzothiadiazole complexes

inferred← citeshttps://doi.org/10.1016/j.dyepig.2023.111533openalex-snapshot

Aryloxy-benzothiadiazole-chalcone and aryloxy-benzothiadiazole-fluorene AIEE luminogens: Synthesis, photophysical properties, and electroluminescence evaluation

inferred← citeshttps://doi.org/10.1016/j.dyepig.2025.112922openalex-snapshot

Polycyclic 1,2,5-chalcogenadiazole dyes: structural, optical, and redox properties in neutral and radical-ion states (chalcogen = S, Se)

inferred← citeshttps://doi.org/10.1016/j.dyepig.2025.113006openalex-snapshot

Isobenzothiadiazole-based dichroic dyes for smart windows

inferred← citeshttps://doi.org/10.1016/j.dyepig.2025.113100openalex-snapshot

Shining a light on benzo[c][1,2,5]thiadiazole photocatalysts

inferred← citeshttps://doi.org/10.1016/j.dyepig.2026.113934openalex-snapshot

Influence of positional isomerism and connector nature on the optical properties of benzothiadiazole-based push-pull chromophores

inferred← citeshttps://doi.org/10.1016/j.electacta.2021.138064openalex-snapshot

Polyhedral oligomeric silsesquioxanes appended conjugated soluble polymers based on thieno[3,4-c]pyrrole-4,6‑dione acceptor unit

inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115395openalex-snapshot

Benzothiadiazole-functionalized Zr-MOF nanosheets enable visible-light mediated photocatalytic oxidation of sulfides in water

inferred← citeshttps://doi.org/10.1016/j.jfluchem.2014.06.019openalex-snapshot

New fluorinated 1,2-diaminoarenes, quinoxalines, 2,1,3-arenothia(selena)diazoles and related compounds

inferred← citeshttps://doi.org/10.1016/j.jfluchem.2016.01.009openalex-snapshot

Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine

inferred← citeshttps://doi.org/10.1016/j.jlumin.2026.121945openalex-snapshot

Photophysical, photochemical and thermodynamic properties of novel linear organic luminophores based on 2,1,3-benzothiadiazole with various donor moieties

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2016.09.016openalex-snapshot

A benzothiadiazole-supported N-heterocyclic carbene and its rhodium and iridium complexes

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2023.122711openalex-snapshot

Organometallic palladium(II) complexes with N-((pyridin-2-yl)methylene)-4-amino-2,1,3-benzothiadiazole: synthesis, characterization and reactivity

inferred← citeshttps://doi.org/10.1016/j.jorganchem.2023.122875openalex-snapshot

Synthesis, characterization and photophysics of polyplatinaynes based on bis(9,9-dibutyl-2,7-fluorenyl)-2,1,3-benzothiadiazole derivatives

inferred← citeshttps://doi.org/10.1016/j.jpowsour.2018.07.001openalex-snapshot

Comparing calendar and cycle life stability of redox active organic molecules for nonaqueous redox flow batteries

inferred← citeshttps://doi.org/10.1016/j.matpr.2020.03.501openalex-snapshot

Theoretical studies of squaraine and functionalized 2,1,3-benzothiadiazole molecules for solar cell applications

inferred← citeshttps://doi.org/10.1016/j.mencom.2018.09.001openalex-snapshot

Charge-transfer chemistry of chalcogen–nitrogen π-heterocycles

inferred← citeshttps://doi.org/10.1016/j.mencom.2020.03.011openalex-snapshot

Role of benzothiadiazole substituents in white electroluminescent single macromolecules of fluorene-based copolymers

inferred← citeshttps://doi.org/10.1016/j.mencom.2024.04.001openalex-snapshot

Recognition and sensing of Lewis bases by 1,2,5-chalcogenadiazoles

inferred← citeshttps://doi.org/10.1016/j.microc.2021.106551openalex-snapshot

A large Stokes shift probe based enhanced ICT strategy for Hg2+-detection in cancer cells and zebrafish

inferred← citeshttps://doi.org/10.1016/j.molliq.2019.04.121openalex-snapshot

Effect of the linkages on the self-assembly and photophysical properties of 4,7-diphenyl-2,1,3-benzothiadiazole-based luminescent polycatenars

inferred← citeshttps://doi.org/10.1016/j.molliq.2020.114277openalex-snapshot

2,1,3-Benzothiadiazole dyes conjugated with benzothiazole and benzoxazole: Synthesis, solvatochromism and solid-state properties

inferred← citeshttps://doi.org/10.1016/j.molliq.2024.125425openalex-snapshot

Click for Light: Synthesis of bent (Benzothiadiazolyl)triazole luminescent liquid crystals via click Chemistry

inferred← citeshttps://doi.org/10.1016/j.molliq.2026.129270openalex-snapshot

2,1,3-benzothiadiazole-based probe exhibits inverted fluorosolvatochromism and aggregation-induced emission

inferred← citeshttps://doi.org/10.1016/j.molstruc.2016.11.050openalex-snapshot

Synthesis, characterization and photophysical properties of luminescent non-symmetric 4-pyridyl benzothiadiazole derivatives

inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.145171openalex-snapshot

Influence of side‑chloro substitution on the thermal and photophysical properties of 2,1,3-benzothiadiazole-based liquid crystals

inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.147599openalex-snapshot

Positive fluorosolvatochromism in N,N-dimethyl-4-amino-2,1,3-benzothiadiazole: A polarity-sensitive fluorescent probe

inferred← citeshttps://doi.org/10.1016/j.optmat.2014.04.019openalex-snapshot

Improvement of intramolecular charge transfer within a donor–acceptor blend by doping novel synthesized benzothiadiazole small molecules in solid state

inferred← citeshttps://doi.org/10.1016/j.orgel.2018.01.022openalex-snapshot

Effects of vinylene and azomethine bridges on optical, theoretical electronic structure and electrical properties of new anthracene and carbazole based π-conjugated molecules

inferred← citeshttps://doi.org/10.1016/j.poly.2017.09.048openalex-snapshot

The hows and whys of peculiar coordination of 4-amino-2,1,3-benzothiadiazole

inferred← citeshttps://doi.org/10.1016/j.poly.2017.11.017openalex-snapshot

Noncovalent interactions and photophysical properties of new Ag(I) complexes with 4-amino-2,1,3-benzothiadiazole

inferred← citeshttps://doi.org/10.1016/j.polymer.2014.04.004openalex-snapshot

Random vs. alternating donor-acceptor copolymers: A comparative study of absorption and field effect mobility

inferred← citeshttps://doi.org/10.1016/j.polymer.2017.11.024openalex-snapshot

Efficient benzodithiophene and thienopyrroledione containing random polymers as components for organic solar cells

inferred← citeshttps://doi.org/10.1016/j.polymer.2025.129056openalex-snapshot

Fluorinated benzo[c][1,2,5]selenadiazole-based electrochromic polymers: Effects of heteroatom substitution and fluorination on performance

inferred← citeshttps://doi.org/10.1016/j.progpolymsci.2017.03.003openalex-snapshot

Recent advances in high performance donor-acceptor polymers for organic photovoltaics

inferred← citeshttps://doi.org/10.1016/j.reactfunctpolym.2018.08.011openalex-snapshot

Benzothiadiazole-based donor–acceptor nanoparticles with solvatochromic and thermoresponsive properties

inferred← citeshttps://doi.org/10.1016/j.rechem.2024.101494openalex-snapshot

Synthesis and evaluation of linearly fused thiadiazolocoumarins as prospects with broad-spectrum bioactivity

inferred← citeshttps://doi.org/10.1016/j.saa.2022.120913openalex-snapshot

Synthesis and application of a highly fluorescent styryl-benzothiadiazole derivative as a chemosensor for ethanol in hydroalcoholic solutions

inferred← citeshttps://doi.org/10.1016/j.saa.2022.122242openalex-snapshot

A naphthol hydrazone Schiff base bearing benzothiadiazole unit for fluorescent detection of Fe3+ in PC3 cells

inferred← citeshttps://doi.org/10.1016/j.saa.2025.126090openalex-snapshot

Rod-like D-π-A-π-D Schiff base liquid crystal for continuous ion sensing, live cell imaging, fingerprint imaging and WLED

inferred← citeshttps://doi.org/10.1016/j.snb.2014.12.056openalex-snapshot

Studies on UV–vis and fluorescence changements in Co2+ and Cu2+ recognition by a new benzimidazole–benzothiadiazole derivative

inferred← citeshttps://doi.org/10.1016/j.snb.2020.127701openalex-snapshot

Highly fluorescent lipophilic 2,1,3-benzothiadiazole fluorophores as optical sensors for tagging material and gasoline adulteration with ethanol

inferred← citeshttps://doi.org/10.1016/j.snb.2020.128530openalex-snapshot

Appending ionic liquids to fluorescent benzothiadiazole derivatives: Light up and selective lysosome staining

inferred← citeshttps://doi.org/10.1016/j.snb.2020.128998openalex-snapshot

A benzothiadiazole-quinoline hybrid sensor for specific bioimaging and surgery procedures in mice

inferred← citeshttps://doi.org/10.1016/j.tet.2014.06.096openalex-snapshot

1,2,5-Thiadiazole 2-oxides: selective synthesis, structural characterization, and electrochemical properties

inferred← citeshttps://doi.org/10.1016/j.tet.2014.06.110openalex-snapshot

Highly emissive dimesitylboryl-substituted 2,1,3-benzothiadiazole derivatives: photophysical properties and efficient fluorescent sensor for fluoride anions

inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.017openalex-snapshot

Substitution effects on the properties of 10,13-disubstituted dipyrido[3,2-a:2′,3′-c]phenazine donor–acceptor compounds and their ruthenium(II) complexes

inferred← citeshttps://doi.org/10.1016/j.tet.2016.04.046openalex-snapshot

Surprising characteristics of D–A-type functional dyes by introducing 4-alkoxythiazoles as the donor-unit

inferred← citeshttps://doi.org/10.1016/j.tet.2018.05.042openalex-snapshot

Synthesis and characterization of non-symmetrical photoswitchable DTE(OMe) sensitizers

inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.106openalex-snapshot

Direct synthesis of fused 1,2,5-selenadiazoles from 1,2,5-thiadiazoles

inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.06.052openalex-snapshot

Phenoxy-benzothiadiazole dyes: Synthesis, photophysical properties and preliminary application in OLEDs

inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.152230openalex-snapshot

Fused 1,2,5-thia- and 1,2,5-selenadiazoles: Synthesis and application in materials chemistry

inferred← citeshttps://doi.org/10.1021/acs.biochem.7b00056openalex-snapshot

The Cation−π Interaction Enables a Halo-Tag Fluorogenic Probe for Fast No-Wash Live Cell Imaging and Gel-Free Protein Quantification

inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.7b00048openalex-snapshot

Specific Imaging of Intracellular Lipid Droplets Using a Benzothiadiazole Derivative with Solvatochromic Properties

inferred← citeshttps://doi.org/10.1021/acs.cgd.0c00253openalex-snapshot

Relationship between Crystal Structure, Crystal Morphology, and Mechanochromic Luminescence of Triphenylimidazolylbenzothiadiazole Derivatives

inferred← citeshttps://doi.org/10.1021/acs.cgd.2c00420openalex-snapshot

Slip-Stacking of Benzothiadiazole Can Provide a Robust Structural Motif for Porous Hydrogen-Bonded Organic Frameworks

inferred← citeshttps://doi.org/10.1021/acs.chemmater.6b02813openalex-snapshot

Benzo[d][1,2,3]thiadiazole (isoBT): Synthesis, Structural Analysis, and Implementation in Semiconducting Polymers

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6b01039openalex-snapshot

Tuning the Rainbow: Systematic Modulation of Donor–Acceptor Systems through Donor Substituents and Solvent

inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6b02863openalex-snapshot

Two 3D Cd(II) Metal–Organic Frameworks Linked by Benzothiadiazole Dicarboxylates: Fantastic S@Cd6 Cage, Benzothiadiazole Antidimmer, and Dual Emission

inferred← citeshttps://doi.org/10.1021/acs.jcim.4c02414openalex-snapshot

Integrating Machine Learning and SHAP Analysis to Advance the Rational Design of Benzothiadiazole Derivatives with Tailored Photophysical Properties

inferred← citeshttps://doi.org/10.1021/acs.joc.0c01031openalex-snapshot

Fluorescent Benzoselenadiazoles: Synthesis, Characterization, and Quantification of Intracellular Lipid Droplets and Multicellular Model Staining

inferred← citeshttps://doi.org/10.1021/acs.joc.0c01805openalex-snapshot

Deciphering the Dynamics of Organic Nanoaggregates with AIEE Effect and Excited States: Lipophilic Benzothiadiazole Derivatives as Selective Cell Imaging Probes

inferred← citeshttps://doi.org/10.1021/acs.joc.2c00641openalex-snapshot

A Series of D–A–D Structured Disilane-Bridged Triads: Structure and Stimuli-Responsive Luminescence Studies

inferred← citeshttps://doi.org/10.1021/acs.joc.5c00536openalex-snapshot

Benzothiadiazole-Centered Donor–Acceptor–Donor Systems: Synthesis, Characterization, and PFAS-Induced Fluorochromism

inferred← citeshttps://doi.org/10.1021/acs.joc.5c02414openalex-snapshot

Benzo[1,2,3]thiadiazole as an Attractive Heteroaromatic Platform for Two-Photon Absorbing (TPA) Fluorophores: TPA Enhancement in Quasi-Quadrupolar S,N-Heteroarene-Cored Dyes via Skeletal Editing and Regioisomeric Control

inferred← citeshttps://doi.org/10.1021/acs.joc.6b00245openalex-snapshot

Synthesis, Structure, Properties, and Bioimaging of a Fluorescent Nitrogen-Linked Bisbenzothiadiazole

inferred← citeshttps://doi.org/10.1021/acs.joc.6b00789openalex-snapshot

Red Phosphorescence from Benzo[2,1,3]thiadiazoles at Room Temperature

inferred← citeshttps://doi.org/10.1021/acs.joc.6b01831openalex-snapshot

4-Amino-2,1,3-benzothiadiazole as a Removable Bidentate Directing Group for the Pd(II)-Catalyzed Arylation/Oxygenation of sp 2 /sp 3 β-C–H Bonds of Carboxamides

inferred← citeshttps://doi.org/10.1021/acs.joc.6b02778openalex-snapshot

Molecular Organization of 2,1,3-Benzothiadiazoles in the Solid State

inferred← citeshttps://doi.org/10.1021/acs.joc.9b00130openalex-snapshot

Palladium Catalyst with Task-Specific Ionic Liquid Ligands: Intracellular Reactions and Mitochondrial Imaging with Benzothiadiazole Derivatives

inferred← citeshttps://doi.org/10.1021/acs.jpca.3c04798openalex-snapshot

Multiconfigurational Calculations and Experimental Resonant Raman/SERRS of a Donor–Acceptor Thiadiazole Dye

inferred← citeshttps://doi.org/10.1021/acs.jpca.5c06566openalex-snapshot

Dynamic Electronic Coupling in the Self-Exchange Charge Transfer Reaction of Benzothiadiazole Redoxmer in Acetonitrile Calculated with Constrained Density Functional Theory

inferred← citeshttps://doi.org/10.1021/acs.jpca.6b00447openalex-snapshot

Benzo[c][1,2,5]thiadiazole Donor–Acceptor Dyes: A Synthetic, Spectroscopic, and Computational Study

inferred← citeshttps://doi.org/10.1021/acs.jpca.8b05361openalex-snapshot

Walking the Emission Tightrope: Spectral and Computational Analysis of Some Dual-Emitting Benzothiadiazole Donor–Acceptor Dyes

inferred← citeshttps://doi.org/10.1021/acs.jpcc.1c07151openalex-snapshot

Fascinating Supramolecular Assembly through Noncovalent Interactions Involving Anions in Organic Ionic Crystals

inferred← citeshttps://doi.org/10.1021/acs.jpcc.2c08663openalex-snapshot

Substituent Effect on Stimuli-Responsive Donor–Acceptor Framework-Based 2-Thiohydantoins for Monitoring Nonanal Vapors

inferred← citeshttps://doi.org/10.1021/acs.jpcc.3c06218openalex-snapshot

Ultra-Photostable Random Lasing Coming from the Benzothiadiazole Derivative Dye-Doped Organic System

inferred← citeshttps://doi.org/10.1021/acs.jpcc.4c01515openalex-snapshot

Thin Films of Conjugated Chalcogenadiazole: Growth, Structure, and Optical Properties of Substituted Selenadiazoloquinoxaline

inferred← citeshttps://doi.org/10.1021/acs.jpcc.5c06408openalex-snapshot

Growth, Structure and Optical Properties of Neat, Bilayer and Codeposited Thin Films: Combining Dibenzoselenadiazoloquinoxaline with Diindenoperylene and Pentacene

inferred← citeshttps://doi.org/10.1021/acs.jpcc.7b04647openalex-snapshot

Spectroscopic Investigation and Theoretical Modeling of Benzothiadiazole-Based Charge-Transfer Chromophores: From Solution to Nanoaggregates

inferred← citeshttps://doi.org/10.1021/acs.jpcc.8b01434openalex-snapshot

Elucidating Factors Controlling Long-Term Stability of Radical Anions for Negative Charge Storage in Nonaqueous Redox Flow Batteries

inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01310openalex-snapshot

Tetrazolo[1,5-a]pyridine-Containing π-Conjugated Systems: Synthesis, Properties, and Semiconducting Characteristics

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03620openalex-snapshot

Pyrazine-Linked End-Functionalized Helicenes: Impact of π-Extension on Frontier Orbital Localization and Chiroptical Properties

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00412openalex-snapshot

Large-Size Star-Shaped Conjugated (Fused) Triphthalocyaninehexaazatriphenylene

inferred← citeshttps://doi.org/10.1021/acsabm.2c01054openalex-snapshot

Biosensors Based on Graphene Oxide Functionalized with Benzothiadiazole-Derived Ligands for the Detection of Cholesterol

inferred← citeshttps://doi.org/10.1021/acsaelm.0c00656openalex-snapshot

Conducting Nanofibers: Diagonal Scrolling of 2D Nanosheets into 1D Nanostructures via In Situ Self-Assembly

inferred← citeshttps://doi.org/10.1021/acsami.0c07586openalex-snapshot

Benzothiadiazole Aryl-amine Based Materials as Efficient Hole Carriers in Perovskite Solar Cells

inferred← citeshttps://doi.org/10.1021/acsami.7b02903openalex-snapshot

Visible-to-NIR Electrochromic Device Prepared from a Thermally Polymerizable Electroactive Organic Monomer

inferred← citeshttps://doi.org/10.1021/acsanm.5c01423openalex-snapshot

Silver Nanoparticles Embedded in COFs as Reusable Photocatalyst for Oxidative Coupling of Benzylic Amine and Carboxylation of Benzyl Alcohol Derivatives

inferred← citeshttps://doi.org/10.1021/acsanm.6c02207openalex-snapshot

Bisphenazine-Based Porous Aromatic Frameworks for Photocatalytic and Electrocatalytic Oxygen Activation

inferred← citeshttps://doi.org/10.1021/acsaom.5c00596openalex-snapshot

Recent Advances in Red and Near-Infrared Organic Room-Temperature Phosphorescent Materials

inferred← citeshttps://doi.org/10.1021/acsapm.5c00012openalex-snapshot

Nitrogen- and Sulfur-Rich Microporous Carbons Derived from Conjugated Microporous Polymers for CO2 Uptake, Supercapacitor Energy Storage, and Electrochemical Hydrogen Production

inferred← citeshttps://doi.org/10.1021/acscatal.8b00407openalex-snapshot

Poly(benzothiadiazoles) and Their Derivatives as Heterogeneous Photocatalysts for Visible-Light-Driven Chemical Transformations

inferred← citeshttps://doi.org/10.1021/acsenergylett.0c01447openalex-snapshot

Fluorescence-Enabled Self-Reporting for Redox Flow Batteries

inferred← citeshttps://doi.org/10.1021/acsomega.5c10011openalex-snapshot

Responsive Supramolecular Sensors Based on Pillar[5]arene–BTD Complexes for Aqueous Sensing: From Static Quenching to Anion and DNA Recognition

inferred← citeshttps://doi.org/10.1021/acsomega.6b00289openalex-snapshot

Synthesis of Near-Infrared Fluorescent Two-Photon-Absorbing Fluorenyl Benzothiadiazole and Benzoselenadiazole Derivatives

inferred← citeshttps://doi.org/10.1021/acsomega.7b00416openalex-snapshot

Preferential Mitochondrial Localization of a Goniothalamin Fluorescent Derivative

inferred← citeshttps://doi.org/10.1021/acsomega.7b01055openalex-snapshot

Synthesis of Salts of 1,2,5,6- and 1,4,5,8-Naphthalenetetramine

inferred← citeshttps://doi.org/10.1021/acsomega.8b00434openalex-snapshot

From Live Cells to Caenorhabditis elegans : Selective Staining and Quantification of Lipid Structures Using a Fluorescent Hybrid Benzothiadiazole Derivative

inferred← citeshttps://doi.org/10.1021/acsphyschemau.5c00118openalex-snapshot

Interplay of Aggregation-Induced Enhanced Emission and Thermally Activated Delayed Fluorescence in Asymmetric Fluorenyl–Benzothiadiazole Derivatives

inferred← citeshttps://doi.org/10.1021/ar500468popenalex-snapshot

Benzothiadiazole Derivatives as Fluorescence Imaging Probes: Beyond Classical Scaffolds

inferred← citeshttps://doi.org/10.1021/jacs.1c04810openalex-snapshot

Linker Engineering toward Full-Color Emission of UiO-68 Type Metal–Organic Frameworks

inferred← citeshttps://doi.org/10.1021/jacs.9b03956openalex-snapshot

Excited-State Dynamics in Fully Conjugated 2D Covalent Organic Frameworks

inferred← citeshttps://doi.org/10.1021/jacsau.5c01768openalex-snapshot

Emissive Room-Temperature Ionic Liquids Enabled by Dialkylphospholium-Based Tetracyclic Cores with Bulky Counter Anions

inferred← citeshttps://doi.org/10.1021/jo4005734openalex-snapshot

Donor–Acceptor Ferrocenyl-Substituted Benzothiadiazoles: Synthesis, Structure, and Properties

inferred← citeshttps://doi.org/10.1021/jo401384gopenalex-snapshot

Asymmetrical/Symmetrical D−π–A/D−π–D Thiazole-Containing Aromatic Heterocyclic Fluorescent Compounds Having the Same Triphenylamino Chromophores

inferred← citeshttps://doi.org/10.1021/jo402111qopenalex-snapshot

Aryl-Substituted Unsymmetrical Benzothiadiazoles: Synthesis, Structure, and Properties

inferred← citeshttps://doi.org/10.1021/jo502773gopenalex-snapshot

Synthesis, Optical Properties, and Electronic Structures of Nucleobase-Containing π-Conjugated Oligomers

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