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化工社化工社 化学情報印刷レポート · 研究参考用
HRID 241472作成日:2026年10月26日

Nitrogen → Azobenzene

https://huagongshe.com/reaction/241472

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物9-[4-[(4-Nonoxyphenyl)diazenyl]phenoxy]nonyl prop-2-enoateHCID 89549536—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物AzobenzeneHCID 2272—

反応条件

温度64 °C

反応手順

The polymer precursors A9AB9 and DA9AB along with the surfactant AC10COONa were used, with the structure of each shown in FIG. 3. The azobenzene nanoparticles were synthesized using a mini-emulsion process. Similar processes have been described in documents 12 through 14. To prepare the instant nanoparticle, 15 mg of surfactant AC10COONa was dissolved in 10 ml of water. 20 mol % of A9AB9 and 80 mol % of DA9AB were mixed with 2 w % 2,2′-azoisobutyronitrile (AIBN) in 2 g of chloroform. The solution was added drop by drop to the surfactant solution and stirred for 1 hour. The mixture was then sonicated in an ice bath for 2 minutes at 90% amplitude using an Ultrasonic Processor (ACE Glass, Inc) with a probe (Model LV261). The resulting mini-emulsion was stirred at room temperature with N2 bubbled into it for 15 min to remove oxygen. With continuous stirring and bubbling of N2, the emulsion was then heated in an oil bath at 64° C. for 6 hours to remove chloroform and promote polymerization. A nanocolloid suspension comprising the desired nanoparticles was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08652352B2
出典データセットuspto-grants-2014_02
ORD IDord-89d5f8b069624e83980fc4878835cdcc
出典メモuspto-grants-2014_02