Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241472Generated: October 25, 2026

Nitrogen → Azobenzene

https://huagongshe.com/reaction/241472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
Reactant9-[4-[(4-Nonoxyphenyl)diazenyl]phenoxy]nonyl prop-2-enoateHCID 89549536—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductAzobenzeneHCID 2272—

Reaction Conditions

Temperature64 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08652352B2
Source datasetuspto-grants-2014_02
ORD IDord-89d5f8b069624e83980fc4878835cdcc
Source noteuspto-grants-2014_02