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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 241472생성일: 2026년 10월 26일

Nitrogen → Azobenzene

https://huagongshe.com/reaction/241472

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참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물9-[4-[(4-Nonoxyphenyl)diazenyl]phenoxy]nonyl prop-2-enoateHCID 89549536—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물AzobenzeneHCID 2272—

반응 조건

온도64 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08652352B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-89d5f8b069624e83980fc4878835cdcc
출처 메모uspto-grants-2014_02