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Synthesis of 1,3,5-Tris(phenylamino) Benzene Derivatives and Experimental and Theoretical Investigations of Their Antioxidation Mechanism
- Source :
- Industrial & Engineering Chemistry Research. 55:1819-1826
- Publication Year :
- 2016
- Publisher :
- American Chemical Society (ACS), 2016.
-
Abstract
- 1,3,5-Tris(phenylamino) benzene and a series of its substitution derivatives were synthesized. The structure of the as-synthesized products was confirmed by nuclear magnetic resonance spectroscopy and high resolution mass spectra. Moreover, the antioxidation behavior of 1,3,5-tris(phenylamino) benzene and its substitution derivatives as antioxidants in several ester oils was evaluated by a rotary oxygen bomb test and pressurized differential scanning calorimetry, while theoretical calculations were conducted to examine their antioxidation mechanism. It was found that 1,3,5-tris(phenylamino) benzene exhibits better antioxidation ability at elevated temperature (150 and 210 °C) than commonly used commercial antioxidant diphenylamine. In the meantime, the substitution groups exhibit significant effects on the antioxidation behavior of 1,3,5-tris(phenylamino) benzene and its derivatives. This is because the substituents result in changes in the molecular structure and electronic effect of the as-synthesized p...
- Subjects :
- General Chemical Engineering
Diphenylamine
chemistry.chemical_element
02 engineering and technology
General Chemistry
Nuclear magnetic resonance spectroscopy
010402 general chemistry
021001 nanoscience & nanotechnology
01 natural sciences
Medicinal chemistry
Oxygen
Industrial and Manufacturing Engineering
0104 chemical sciences
chemistry.chemical_compound
Differential scanning calorimetry
chemistry
Electronic effect
Mass spectrum
Organic chemistry
Molecule
0210 nano-technology
Benzene
Subjects
Details
- ISSN :
- 15205045 and 08885885
- Volume :
- 55
- Database :
- OpenAIRE
- Journal :
- Industrial & Engineering Chemistry Research
- Accession number :
- edsair.doi...........741cb33cea2f9307c2c19f342eff3cf6
- Full Text :
- https://doi.org/10.1021/acs.iecr.5b04295