4,7‐Dimethyl‐4,7‐dihydro[1,2,5]thiadiazolo[3,4‐<i>b</i>]‐pyrazin, ein neuer Elektronendonor mit einem 12π‐Elektronensystem

Yamashita, Yoshiro; Eguchi, Junko; Suzuki, Takanori; Kabuto, Chizuko; Miyashi, Tsutomu; Tanaka, Shoji

doi:10.1002/ange.19901020629

Cited by 3 publications

(1 citation statement)

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“…Benzidine‐type electron donors fused with bis‐2,1,3‐chalcogenediazole units (Scheme ) were synthesized 66b. Electrostatic interactions between heterocycles may be a useful tool, which is suggested by various types of molecular networks formed by the chalcogen–nitrogen contacts in the crystals of 2,1,3‐chalcogenadiazole derivatives 66c,66d. Derivatives 62a , b and 64a , b displayed multistage redox behavior.…”

Section: Synthesis Chemical Properties Sulfur Extrusion and Mismentioning

confidence: 99%

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

et al. 2012

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2,1,3‐Benzothiadiazole (BTD) is one of the most important nuclei used in the chemistry of photoluminescent compounds and applicable for light technology. The understanding of its properties and reactions is fundamental for the design and application of these derivatives in molecular organic electronic devices and for other technologies. As a result of their potential as constituents of organic light‐emitting diodes, solar cells, liquid crystals, dyes, photovoltaic cells, and many others, attention has been focused on BTD π‐extended derivatives with potential use in this exciting area. Herein, we describe their syntheses, properties, reactions, and selected examples of applications in light technology using by BTD (small molecules) as the core.

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Section: Synthesis Chemical Properties Sulfur Extrusion and Mismentioning

confidence: 99%