Expression of anti-Kasha's emission from amino benzothiadiazole and its utilization for fluorescent chemosensors and organic light emitting materials

Borylated Arylamine–Benzothiadiazole Donor–Acceptor Materials as Low-LUMO, Low-Band-Gap Chromophores

(2017) Daniel L. Crossley et al.   ORGANOMETALLICS

Charge carrier mobility in one-dimensional aligned π-stacks of conjugated small molecules with a benzothiadiazole central unit

(2017) Deyan Raychev et al.   PHYSICAL CHEMISTRY CHEMICAL PHYSICS

Teaching an old acceptor new tricks: rationally employing 2,1,3-benzothiadiazole as input to design a highly efficient red thermally activated delayed fluorescence emitter

(2017) Fan Ni et al.   Journal of Materials Chemistry C

The Strong Light-Emission Materials in the Aggregated State: What Happens from a Single Molecule to the Collective Group

(2017) Qianqian Li et al.   Advanced Science

“Wine-Dark Sea” in an Organic Flow Battery: Storing Negative Charge in 2,1,3-Benzothiadiazole Radicals Leads to Improved Cyclability

(2017) Wentao Duan et al.   ACS Energy Letters

Difluorobenzothiadiazole-Based Small-Molecule Organic Solar Cells with 8.7% Efficiency by Tuning of π-Conjugated Spacers and Solvent Vapor Annealing

(2016) Jin-Liang Wang et al.   ADVANCED FUNCTIONAL MATERIALS

Asymmetric-Indenothiophene-Based Copolymers for Bulk Heterojunction Solar Cells with 9.14% Efficiency

(2016) Meng Wang et al.   ADVANCED MATERIALS

Effect of Systematically Tuning Conjugated Donor Polymer Lowest Unoccupied Molecular Orbital Levels via Cyano Substitution on Organic Photovoltaic Device Performance

(2016) Abby Casey et al.   CHEMISTRY OF MATERIALS

Novel 2,1,3-benzothiadiazole derivatives used as selective fluorescent and colorimetric sensors for fluoride ion

(2016) Jiefei Wu et al.   DYES AND PIGMENTS

Excited-state intramolecular proton-transfer reaction demonstrating anti-Kasha behavior

(2016) Huan-Wei Tseng et al.   Chemical Science

Enhancing the power conversion efficiency of polymer solar cells to 9.26% by a synergistic effect of fluoro and carboxylate substitution

(2016) Yahui Liu et al.   Journal of Materials Chemistry A

Benzothiadiazole building units in solution-processable small molecules for organic photovoltaics

(2016) Jia Du et al.   Journal of Materials Chemistry A

Benzothiadiazole Derivatives as Fluorescence Imaging Probes: Beyond Classical Scaffolds

(2015) Brenno A. D. Neto et al.   ACCOUNTS OF CHEMICAL RESEARCH

Medium Bandgap Conjugated Polymer for High Performance Polymer Solar Cells Exceeding 9% Power Conversion Efficiency

(2015) Jae Woong Jung et al.   ADVANCED MATERIALS

Enhancing electron affinity and tuning band gap in donor–acceptor organic semiconductors by benzothiadiazole directed C–H borylation

(2015) D. L. Crossley et al.   Chemical Science

Preparation of aggregation-induced emission dots for long-term two-photon cell imaging

(2015) Qiang Ye et al.   Journal of Materials Chemistry B

New Molecular Donors with Dithienopyrrole as the Electron-Donating Group for Efficient Small-Molecule Organic Solar Cells

(2014) Hung-I Lu et al.   CHEMISTRY OF MATERIALS

Designed Benzothiadiazole Fluorophores for Selective Mitochondrial Imaging and Dynamics

(2014) Pedro H. P. R. Carvalho et al.   CHEMISTRY-A EUROPEAN JOURNAL

A study on the photophysics of 9-amino-10-cyanoanthracene: probing its dual absorption and emission behavior

(2014) Sharmistha Dutta Choudhury et al.   PHYSICAL CHEMISTRY CHEMICAL PHYSICS

Oligothiophene-Bridged Bis(arylene ethynylene) Small Molecules for Solution-Processible Organic Solar Cells with High Open-Circuit Voltage

(2013) Qian Liu et al.   Chemistry-An Asian Journal

Controllable Direct Arylation: Fast Route to Symmetrical and Unsymmetrical 4,7-Diaryl-5,6-difluoro-2,1,3-benzothiadiazole Derivatives for Organic Optoelectronic Materials

(2013) Junxiang Zhang et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

On the dual emission of p-dimethylaminobenzonitrile and its photophysical implications

(2013) Javier Catalán   PHYSICAL CHEMISTRY CHEMICAL PHYSICS

Molecular Design of Photovoltaic Materials for Polymer Solar Cells: Toward Suitable Electronic Energy Levels and Broad Absorption

(2012) Yongfang Li   ACCOUNTS OF CHEMICAL RESEARCH

Controlling growth of molecular crystal aggregates for efficient optical waveguides

(2012) Songhua Chen et al.   CHEMICAL COMMUNICATIONS

D–π–A–π–D type benzothiadiazole–triphenylamine based small molecules containing cyano on the π-bridge for solution-processed organic solar cells with high open-circuit voltage

(2012) Shaohang Zeng et al.   CHEMICAL COMMUNICATIONS

Organic Sensitizers Including π-Conjugated Fluorene–Benzothiadiazole Bridge for Dye-sensitized Solar Cells

(2012) Mutsumi Kimura et al.   CHEMISTRY LETTERS

What Determines the Rate of Excited-State Intramolecular Electron-Transfer Reaction of 4-(N,N′-dimethylamino)benzonitrile in Room Temperature Ionic Liquids? A Study in [bmim][PF6]

(2012) Kotni Santhosh et al.   CHEMPHYSCHEM

High-performance dye-sensitized solar cells based on 5,6-bis-hexyloxy-benzo[2,1,3]thiadiazole

(2012) Hsien-Hsin Chou et al.   JOURNAL OF MATERIALS CHEMISTRY

Solution-Processed Organic Solar Cells with Power Conversion Efficiencies of 2.5% using Benzothiadiazole/Imide-Based Acceptors

(2011) Jason T. Bloking et al.   CHEMISTRY OF MATERIALS

Synthesis and applications of difluorobenzothiadiazole based conjugated polymers for organic photovoltaics

(2011) Zhao Li et al.   JOURNAL OF MATERIALS CHEMISTRY

Ultrahigh Mobility in Polymer Field-Effect Transistors by Design

(2011) Hoi Nok Tsao et al.   JOURNAL OF THE AMERICAN CHEMICAL SOCIETY

Synthesis, properties and highly selective mitochondria staining with novel, stable and superior benzothiadiazole fluorescent probes

(2011) Brenno A. D. Neto et al.   RSC Advances

A Low-Bandgap Diketopyrrolopyrrole-Benzothiadiazole-Based Copolymer for High-Mobility Ambipolar Organic Thin-Film Transistors

(2010) Prashant Sonar et al.   ADVANCED MATERIALS

Luminescent 2,1,3-benzothiadiazole-based liquid crystalline compounds

(2007) André A. Vieira et al.   JOURNAL OF MOLECULAR STRUCTURE